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Chemical compound
Acetophenone is the organic compound with the formula C6H5C(O)CH3. It is the simplest aromatic ketone. This colorless, viscous liquid is a precursor to
Acetophenone
Index of chemical compounds with the same name
Hydroxyacetophenone may refer to: 2-Hydroxyacetophenone (o-hydroxyacetophenone) 3-Hydroxyacetophenone (m-hydroxyacetophenone) 4-Hydroxyacetophenone (p
Hydroxyacetophenone
Chemical compound
synthetic ketone fragrance also known as OTNE (octahydrotetramethyl acetophenone) and by other commercial trade names such as: Iso E Super, Iso Gamma
Tetramethyl acetyloctahydronaphthalenes
Tetramethyl_acetyloctahydronaphthalenes
Class of enzymes
Acetophenone carboxylase (EC 6.4.1.8) is an enzyme with systematic name acetophenone:carbon-dioxide ligase (ADP-forming). This enzyme catalyses the following
Acetophenone_carboxylase
Riot control agent
chloride, also commonly known as chloroacetophenone, is a substituted acetophenone. It is a useful building block in organic chemistry. Apart from that
Phenacyl_chloride
functional group which is composed of the cyclic ketal of a diol with acetophenone. In pharmaceutical chemistry, it is present in algestone acetophenide
Acetophenide
Phenolic compound found in Norway spruces
Piceol is a phenolic compound found in the needles and in mycorrhizal roots of Norway spruces (Picea abies). Picein is the glucoside of piceol. In the
Piceol
Chemical compound
an organic compound with the formula CH3C6H4C(O)CH3. It is related to acetophenone with a methyl group at the 4-position. Two isomers, 2-methylacetophenone
4-Methylacetophenone
Type of aldol condensation reaction
more electrophilic than any unenolized acetophenone in solution. Therefore, the enolate formed from acetophenone will always preferentially attack the
Self-condensation
Topics referred to by the same term
nervous system Cranial nerves, CN 0 to CN XII CN gas, a substituted acetophenone used as a riot control agent Copernicium, symbol Cn, a chemical element
CN
Behavioral paradigm in which organisms learn to predict aversive events
transgenerationally. In one experiment, mice were conditioned to fear an acetophenone odor and then set up to breed subsequent generations of mice. Those subsequent
Fear_conditioning
Chemical compound
with the formula CH3OC6H4C(O)CH3. It can be viewed as derivative of acetophenone and of anisole. It has an aroma described as sweet, fruity, nutty, and
Acetanisole
Chemical reaction
concentrated ammonium hydroxide and pyridine) is the conversion of acetophenone to 2-phenylacetamide and phenylacetic acid The related Willgerodt–Kindler
Willgerodt_rearrangement
Intravenous medication used in anesthesia
Mecloqualone Methaqualone Methylmethaqualone Nitromethaqualone SL-164 Others Acetophenone Acetylglycinamide chloral hydrate Bromide compounds Lithium bromide Potassium
Propofol
Fluid produced by beavers
activity, of which the phenols 4-ethylphenol and catechol and the ketones acetophenone and 3-hydroxyacetophenone are strongest. Five additional compounds elicit
Castoreum
Chemical compound
Acetosyringone is a phenolic natural product and a chemical compound related to acetophenone and 2,6-dimethoxyphenol. It was first described in relation to
Acetosyringone
Aromatic organic chemical compound
Products of decomposition of cumene hydroperoxide are methylstyrene, acetophenone, and 2-phenylpropan-2-ol. It is produced by treatment of cumene with
Cumene_hydroperoxide
Organic compound with formula (CH3CO)2O
accelerate the reaction. Illustrative are the conversions of benzene to acetophenone and ferrocene to acetylferrocene: (C5H5)2Fe + (CH3CO)2O → (C5H5)Fe(C5H4COCH3)
Acetic_anhydride
Chemical compound
precursor to other organic compounds. It is prepared by bromination of acetophenone: C6H5C(O)CH3 + Br2 → C6H5C(O)CH2Br + HBr The compound was first reported
Phenacyl_bromide
Chemical compound
Ethyl methylphenylglycidate is usually prepared by the condensation of acetophenone and the ethyl ester of monochloroacetic acid in the presence of a base
Ethyl_methylphenylglycidate
Chemical compound
and endives. Racemic 1-phenylethanol is produced by the reduction of acetophenone by sodium borohydride. Alternatively, benzaldehyde can be reacted with
1-Phenylethanol
Industrial process
Byproducts of the cumene process to produce phenol and acetone are acetophenone and alpha-methylstyrene. Bisphenol A Dow process (phenol) Friedel Crafts
Cumene_process
Alternate scientific theory of scent perception
(fruit fly), which is ordinarily attracted to acetophenone, spontaneously dislikes deuterated acetophenone. This dislike increases with the number of deuteriums
Vibration_theory_of_olfaction
Class of CNS depressant drugs
Mecloqualone Methaqualone Methylmethaqualone Nitromethaqualone SL-164 Others Acetophenone Acetylglycinamide chloral hydrate Bromide compounds Lithium bromide Potassium
Benzodiazepine
Obsolete sedative–hypnotic drug
Mecloqualone Methaqualone Methylmethaqualone Nitromethaqualone SL-164 Others Acetophenone Acetylglycinamide chloral hydrate Bromide compounds Lithium bromide Potassium
Methaqualone
Rule for predicting outcomes of some addition reactions
in the hydration of phenylacetylene by auric catalysis, which gives acetophenone; although with a special ruthenium catalyst it provides the other regioisomer
Markovnikov's_rule
Disorder causing trouble with sleeping
Mecloqualone Methaqualone Methylmethaqualone Nitromethaqualone SL-164 Others Acetophenone Acetylglycinamide chloral hydrate Bromide compounds Lithium bromide Potassium
Insomnia
Pharmaceutical compound
names βk-NMPEA; FTS-096; FTS096; Methylaminoacetophenone; 2-(Methylamino)acetophenone; NM-AcP; MAA Drug class Norepinephrine–dopamine releasing agent Identifiers
Β-Keto-N-methylphenethylamine
Chemical reaction; acid hydrolysis of a nitroalkane salt to a ketone
converted the potassium salt of 1-phenylnitroethane with sulfuric acid to acetophenone. The reaction mechanism starting from the nitronate salt as the resonance
Nef_reaction
Starch pearls used as food
chemicals were found in the samples. Chemicals found included styrene, acetophenone, and brominated substances, which were not permitted as food additives
Tapioca_pearl
Antispasmodic drug
2-(1-piperidino)propiophenone is synthesized in turn by the aminomethylation of acetophenone using paraformaldehyde and piperidine in a Mannich reaction. In the second
Trihexyphenidyl
Chemical rearrangement
The Beckmann rearrangement scheme for acetophenone oxime under oxonium–acetic acid complex and hydronium–water complex.
Beckmann_rearrangement
Chemical compound
is an organic compound with the formula C9H8O. It is prepared using acetophenone, formaldehyde, and an amine hydrochloride in a Mannich reaction. It can
Acrylophenone
Medication for parasite infestations
Methylmethaqualone Nitromethaqualone SL-164 Volatiles/gases Acetone Acetophenone Acetylglycinamide chloral hydrate Aliflurane Benzene Butane Butylene
Ivermectin
Chemical compound
Mecloqualone Methaqualone Methylmethaqualone Nitromethaqualone SL-164 Others Acetophenone Acetylglycinamide chloral hydrate Bromide compounds Lithium bromide Potassium
Lemborexant
Phenomenon in chemistry
acts as a radical initiator. Carbonyl impurities in the polymer (cf. acetophenone) also absorb light in the near ultraviolet range (300 to 400 nm), forming
Photo-oxidation_of_polymers
Conversion of a carbonyl to an amine
example of this reaction is the synthesis of 1-phenylethylamine from acetophenone: Additionally, many systems catalyze reductive aminations with hydrogenation
Reductive_amination
Drug that reduces excitement without inducing sleep
Mecloqualone Methaqualone Methylmethaqualone Nitromethaqualone SL-164 Others Acetophenone Acetylglycinamide chloral hydrate Bromide compounds Lithium bromide Potassium
Sedative
Chemical compound
imines. 1-Phenylethylamine may be prepared by the reductive amination of acetophenone: C6H5C(O)CH3 + NH3 + H2 → C6H5CH(NH2)CH3 + H2O The Leuckart reaction
1-Phenylethylamine
Benzodiazepine medication
Mecloqualone Methaqualone Methylmethaqualone Nitromethaqualone SL-164 Others Acetophenone Acetylglycinamide chloral hydrate Bromide compounds Lithium bromide Potassium
Lorazepam
Phenethylamine derivative
(β-hydroxyphenethylamine) N-Methylphenethylamine β-Keto-N-methylphenethylamine Acetophenone Katz DP, Bhattacharya D, Bhattacharya S, Deruiter J, Clark CR, Suppiramaniam
2-Aminoacetophenone
Benzodiazepine sedative
Methylmethaqualone Nitromethaqualone SL-164 Volatiles/gases Acetone Acetophenone Acetylglycinamide chloral hydrate Aliflurane Benzene Butane Butylene
Diazepam
Preference of chemical bonding or breaking in one direction over others
according to Markovnikov's rule). For example, in a study involving acetophenones, this oxygen was preferentially inserted between the carbonyl and the
Regioselectivity
Sleep medication
Mecloqualone Methaqualone Methylmethaqualone Nitromethaqualone SL-164 Others Acetophenone Acetylglycinamide chloral hydrate Bromide compounds Lithium bromide Potassium
Zolpidem
Hydrocarbon compound; precursor to styrene and polystyrene
Once inside the body, ethylbenzene biodegrades to 1-phenylethanol, acetophenone, phenylglyoxylic acid, mandelic acid, benzoic acid and hippuric acid
Ethylbenzene
Chemical compound
Methylmethaqualone Nitromethaqualone SL-164 Volatiles/gases Acetone Acetophenone Acetylglycinamide chloral hydrate Aliflurane Benzene Butane Butylene
SAGE-324
Benzodiazepine research chemical
Mecloqualone Methaqualone Methylmethaqualone Nitromethaqualone SL-164 Others Acetophenone Acetylglycinamide chloral hydrate Bromide compounds Lithium bromide Potassium
Pynazolam
Chemical compound
sunscreen products. DBM is prepared by condensation of ethyl benzoate with acetophenone. Like other 1,3-diketones (or their enols), DBM condenses with a variety
Dibenzoylmethane
Chemical compound
susceptibility (χ) −83.73·10−6 cm3/mol Related compounds Related ketones Acetophenone Butyrophenone Except where otherwise noted, data are given for materials
Propiophenone
Pharmaceutical compound
Methylmethaqualone Nitromethaqualone SL-164 Volatiles/gases Acetone Acetophenone Acetylglycinamide chloral hydrate Aliflurane Benzene Butane Butylene
CF2-Etomidate
Chemical compound
compound with the chemical formula C 12H 8O. The structure contains acetophenone and a polyyne (pentadiynyl) portion, conjugated together as an ynone
Capillin
Class of depressant drugs derived from barbituric acid
Mecloqualone Methaqualone Methylmethaqualone Nitromethaqualone SL-164 Others Acetophenone Acetylglycinamide chloral hydrate Bromide compounds Lithium bromide Potassium
Barbiturate
Topics referred to by the same term
protein, a non-sperm component of semen Acepromazine, veterinary sedative Acetophenone, a chemical compound ACP1 (low molecular weight phosphotyrosine protein
ACP
Index of chemical compounds with the same molecular formula
C8H8O (molar mass: 120.15 g/mol, exact mass: 120.057515 u) may refer to: Acetophenone Methylbenzaldehydes 2-Methylbenzaldehyde 3-Methylbenzaldehyde 4-Methylbenzaldehyde
C8H8O
Benzodiazepine medication
Methylmethaqualone Nitromethaqualone SL-164 Volatiles/gases Acetone Acetophenone Acetylglycinamide chloral hydrate Aliflurane Benzene Butane Butylene
Alprazolam
Organic compound with a –C(=O)Cl group
(MeMgBr), 2-phenyl-2-propanol (3) is obtained in excellent yield. Although acetophenone (2) is an intermediate in this reaction, it is impossible to isolate
Acyl_chloride
Camera parts, features and technologies
products and UV radiation, producing substituted chlorinated phenols and acetophenones, which are known for their toxicity. Some organic UV filters under UV
UV_filter
Naming convention for stereoisomers of molecules
Re-face and Si-face. In the example displayed on the right, the compound acetophenone is viewed from the Re-face. Hydride addition as in a reduction process
Cahn–Ingold–Prelog priority rules
Cahn–Ingold–Prelog_priority_rules
Benzodiazepine used for anesthesia and procedural sedation
Mecloqualone Methaqualone Methylmethaqualone Nitromethaqualone SL-164 Others Acetophenone Acetylglycinamide chloral hydrate Bromide compounds Lithium bromide Potassium
Midazolam
Species of plant
Mecloqualone Methaqualone Methylmethaqualone Nitromethaqualone SL-164 Others Acetophenone Acetylglycinamide chloral hydrate Bromide compounds Lithium bromide Potassium
Kava
Thienotriazolodiazepine drug
Mecloqualone Methaqualone Methylmethaqualone Nitromethaqualone SL-164 Others Acetophenone Acetylglycinamide chloral hydrate Bromide compounds Lithium bromide Potassium
Brotizolam
Chemical compound
phenyl (C6D5) group may be purchased commercially, such as aniline, acetophenone, nitrobenzene, bromobenzene, and more. International Union of Pure and
Deuterated_benzene
Chemical compound
methods have been used to make tropic acid, for example starting from acetophenone (1). Tropic acid is used in the chemical synthesis of atropine and hyoscyamine
Tropic_acid
Chemical group (–N=C=S)
"Improved approaches in the synthesis of new 2-(1, 3-thiazolidin-2Z-ylidene)acetophenones". Arkivoc. 2005 (6): 356–365. doi:10.3998/ark.5550190.0006.631. hdl:2027/spo
Isothiocyanate
Chemical compound
Mecloqualone Methaqualone Methylmethaqualone Nitromethaqualone SL-164 Others Acetophenone Acetylglycinamide chloral hydrate Bromide compounds Lithium bromide Potassium
Paraldehyde
Chemical sedative and hypnotic drug
Mecloqualone Methaqualone Methylmethaqualone Nitromethaqualone SL-164 Others Acetophenone Acetylglycinamide chloral hydrate Bromide compounds Lithium bromide Potassium
Chloral_hydrate
Chemical compound
presence of gold or mercury reagents, phenylacetylene hydrates to give acetophenone: PhC2H + H2O → PhC(O)CH3 Alkyne Alkyne trimerisation Bordwell, F.G. (1988)
Phenylacetylene
Ionic compound (KBr)
Mecloqualone Methaqualone Methylmethaqualone Nitromethaqualone SL-164 Others Acetophenone Acetylglycinamide chloral hydrate Bromide compounds Lithium bromide Potassium
Potassium_bromide
Chemical compound
names α-Hydroxyacetosyringone 3',5'-Dimethoxy-4'-hydroxy-(2-hydroxy)acetophenone Identifiers CAS Number 90426-22-5 Y 3D model (JSmol) Interactive image
Danielone
Pharmaceutical compound
Methylmethaqualone Nitromethaqualone SL-164 Volatiles/gases Acetone Acetophenone Acetylglycinamide chloral hydrate Aliflurane Benzene Butane Butylene
CF3-Propoxate
Class of enzymes
following chemical reaction: (S)-1-phenylethanol + NAD+ H+ H+ acetophenone + NADH The enzyme is involved in degradation of ethylbenzene. Kniemeyer
(S)-1-phenylethanol dehydrogenase
(S)-1-phenylethanol_dehydrogenase
Primary alcohol compound (CH3CH2CH2OH)
Mecloqualone Methaqualone Methylmethaqualone Nitromethaqualone SL-164 Others Acetophenone Acetylglycinamide chloral hydrate Bromide compounds Lithium bromide Potassium
1-Propanol
Organic compound (CH3OC6H5) also named methoxybenzene
4-methoxyacetophenone: CH3OC6H5 + (CH3CO)2O → CH3OC6H4C(O)CH3 + CH3CO2H Unlike most acetophenones, but reflecting the influence of the methoxy group, methoxyacetophenone
Anisole
System for naming organic chemical compounds
carbonyl group as separate words followed by the word ketone. Acetone Acetophenone Benzophenone Ethyl isopropyl ketone Diethyl ketone The first three of
IUPAC nomenclature of organic chemistry
IUPAC_nomenclature_of_organic_chemistry
Primary male sex hormone
Methylmethaqualone Nitromethaqualone SL-164 Volatiles/gases Acetone Acetophenone Acetylglycinamide chloral hydrate Aliflurane Benzene Butane Butylene
Testosterone
Hydrocarbon compound (C6H6)
Methylmethaqualone Nitromethaqualone SL-164 Volatiles/gases Acetone Acetophenone Acetylglycinamide chloral hydrate Aliflurane Benzene Butane Butylene
Benzene
Chemical compound
is usually prepared by an aldol condensation between benzaldehyde and acetophenone. This reaction, which can be carried out without any solvent, is so reliable
Chalcone
Colourless non-flammable greenhouse gas
Methylmethaqualone Nitromethaqualone SL-164 Volatiles/gases Acetone Acetophenone Acetylglycinamide chloral hydrate Aliflurane Benzene Butane Butylene
Nitrous_oxide
Benzodiazepine medication
Methylmethaqualone Nitromethaqualone SL-164 Volatiles/gases Acetone Acetophenone Acetylglycinamide chloral hydrate Aliflurane Benzene Butane Butylene
Clonazepam
Organic compounds of the form >C=O
center. Acetone and benzophenone ((C6H5)2CO) are symmetrical ketones. Acetophenone (C6H5C(O)CH3) is an unsymmetrical ketone. Many kinds of diketones are
Ketone
SSRI antidepressant
Methylmethaqualone Nitromethaqualone SL-164 Volatiles/gases Acetone Acetophenone Acetylglycinamide chloral hydrate Aliflurane Benzene Butane Butylene
Fluoxetine
Triazolobenzodiazepine drug
Methylmethaqualone Nitromethaqualone SL-164 Volatiles/gases Acetone Acetophenone Acetylglycinamide chloral hydrate Aliflurane Benzene Butane Butylene
Flubromazolam
Flammable organic fuel (C4H10)
Methylmethaqualone Nitromethaqualone SL-164 Volatiles/gases Acetone Acetophenone Acetylglycinamide chloral hydrate Aliflurane Benzene Butane Butylene
Butane
Chemical compound
Mecloqualone Methaqualone Methylmethaqualone Nitromethaqualone SL-164 Others Acetophenone Acetylglycinamide chloral hydrate Bromide compounds Lithium bromide Potassium
Tert-Butyl_alcohol
Italian-Argentinian Bioelectronics and fragrance scientist
to support this prediction, with human subjects unable to distinguish acetophenone and its deuterated counterpart. The study was accompanied by an editorial
Luca_Turin
Triazolobenzodiazepine class medication
Mecloqualone Methaqualone Methylmethaqualone Nitromethaqualone SL-164 Others Acetophenone Acetylglycinamide chloral hydrate Bromide compounds Lithium bromide Potassium
Triazolam
Novel anticonvulsant and anxiolytic
Methylmethaqualone Nitromethaqualone SL-164 Volatiles/gases Acetone Acetophenone Acetylglycinamide chloral hydrate Aliflurane Benzene Butane Butylene
KRM-II-81
Antidepressant medication
Mecloqualone Methaqualone Methylmethaqualone Nitromethaqualone SL-164 Others Acetophenone Acetylglycinamide chloral hydrate Bromide compounds Lithium bromide Potassium
Mirtazapine
Chemical compound
2-Methoxyethanol),(1-Octanol + N,N-Dimethylacetamide), and (1-Octanol + Acetophenone) at Temperatures of (298.15, 308.15, and 318.15) K". Journal of Chemical
1-Octanol
Barbiturate
Mecloqualone Methaqualone Methylmethaqualone Nitromethaqualone SL-164 Others Acetophenone Acetylglycinamide chloral hydrate Bromide compounds Lithium bromide Potassium
Amobarbital
Species of plant in Erythroxylaceae family
having the following phytochemicals with potential drug use: Two new acetophenone diglycosides, erythroxylosides A and B; two known flavans, one known
Erythroxylum_cambodianum
Chemical reaction
synthesis, is a chemical reaction that forms a 2-aryl-indole from an α-bromo-acetophenone and excess aniline; it is named after August Bischler and Richard Möhlau [de]
Bischler–Möhlau indole synthesis
Bischler–Möhlau_indole_synthesis
Drug whose use induces sleep
Mecloqualone Methaqualone Methylmethaqualone Nitromethaqualone SL-164 Others Acetophenone Acetylglycinamide chloral hydrate Bromide compounds Lithium bromide Potassium
Hypnotic
Mixture of fragrant substance
of perfumes may cause allergic reactions of the skin. For instance, acetophenone, ethyl acetate[citation needed] and acetone while present in many perfumes
Perfume
Reaction in organic chemistry
the active form of the ruthenium catalyst complex is generated from 1, acetophenone coordinates to the complex via its carbonyl oxygen and agostically via
Murai_reaction
Class of organosilicon compounds of the form R3Si–O–CR=CR2
2, 6-bis-[ω-trimethylsiloxypolydimethylsiloxy-2′-dimethylsilylethyl] acetophenone. Polymer, 43(1), 29-35. doi:10.1016/S0032-3861(01)00602-4 (a) Wohl, R
Silyl_enol_ether
CH3OH; simplest possible alcohol
Methylmethaqualone Nitromethaqualone SL-164 Volatiles/gases Acetone Acetophenone Acetylglycinamide chloral hydrate Aliflurane Benzene Butane Butylene
Methanol
Chemical compound
Valerophenone is also an inhibitor of the enzyme carbonyl reductase. Acetophenone Butyrophenone Propiophenone Milstein, D.; Stille, J. K. (1978). "A general
Valerophenone
Hypnotic medication
Mecloqualone Methaqualone Methylmethaqualone Nitromethaqualone SL-164 Others Acetophenone Acetylglycinamide chloral hydrate Bromide compounds Lithium bromide Potassium
Eszopiclone
Organic reaction which inserts an alkene into a C-H bond of ethylene
reaction, which involves the insertion of alkenes into a C-H bond of acetophenone. The keto group directs the regiochemistry, stabilizing an aryl intermediate
Hydrovinylation
ACETOPHENONE
ACETOPHENONE
ACETOPHENONE
ACETOPHENONE
Boy/Male
Muslim
Plowman. Tiller. Old Arabic name.
Girl/Female
African, American, Australian, British, Chinese, Danish, English, Finnish, French, German, Greek, Indian, Parsi, Scandinavian, Scottish, Swedish
Thor Flight; Untamed; God of Battle; Thor's Struggle; Land; Light; Deity; Warrior
Boy/Male
Tamil
Bala Mohan | பாலாமோஹந
One who is attractive
Girl/Female
Arabic, Muslim
Pearls
Boy/Male
Assamese, Indian
Knowledge
Boy/Male
Spanish Teutonic
warrior.
Girl/Female
Hindu, Indian, Marathi, Sanskrit
Messenger of Love
Girl/Female
Tamil
Harijatha | ஹரிஜாதா
Fair haired
Boy/Male
Australian, Dutch, French, German, Norse, Russian, Scandinavian, Swedish
Ing's Soldier; Famous Ing-god
Boy/Male
Hindu
Radha and Lord Krishna
ACETOPHENONE
ACETOPHENONE
ACETOPHENONE
ACETOPHENONE
ACETOPHENONE