PHENACYLAMINE

Details

Stereochemistry	ACHIRAL
Molecular Formula	C8H9NO
Molecular Weight	135.1632
Optical Activity	NONE
Defined Stereocenters	0 / 0
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure Search

SMILES

NCC(=O)C1=CC=CC=C1

InChI

InChIKey=HEQOJEGTZCTHCF-UHFFFAOYSA-N

InChI=1S/C8H9NO/c9-6-8(10)7-4-2-1-3-5-7/h1-5H,6,9H2

HIDE SMILES / InChI

Molecular Formula	C8H9NO
Molecular Weight	135.1632
Charge	0
Count

Stereochemistry	ACHIRAL
Additional Stereochemistry	No
Defined Stereocenters	0 / 0
E/Z Centers	0
Optical Activity	NONE

Approval Year

Targets

Primary Target	Pharmacology	Condition	Potency
cytochrome P450 2A19 2 Target ID: 403149.0 Gene Symbol: CYP2A19 Sources: https://www.ncbi.nlm.nih.gov/pubmed/30599194	Inhibitor 8297
Cytochrome P450 2E1 25 Target ID: P79383 Gene ID: 403216.0 Gene Symbol: CYP2E1 Target Organism: Sus scrofa (Pig) Sources: https://www.ncbi.nlm.nih.gov/pubmed/30599194	Inhibitor 8297

PubMed

Title	Date	PubMed
Pyriform cortex beta-waves: odor-specific sensitization following repeated olfactory stimulation.	2001 Feb 23	11172777
Palatability of bird repellents to Rattus norvegicus.	2001 Jul	11464793
Comparison of key aroma compounds in cooked brown rice varieties based on aroma extract dilution analyses.	2002 Feb 27	11853489
"Untypical aging off-flavor" in wine: synthesis of potential degradation compounds of indole-3-acetic acid and kynurenine and their evaluation as precursors of 2-aminoacetophenone.	2002 Jul 17	12105962
Analysis of ketones by selected ion flow tube mass spectrometry.	2003	14648904
Possible coding for recognition of sexes, individuals and species in anal gland volatiles of Mustela eversmanni and M. sibirica.	2003 Jun	12826534
Characteristic aroma components of rennet casein.	2003 Nov 5	14582977
Transformation of 2-aminoacetophenone to ( S) -2-amino-1-phenylethanol by Arthrobacter sulfureus.	2004 Aug	15483382
Synthetic applicability and in situ recycling of a B-methoxy oxazaborolidine catalyst derived from cis-1-amino-indan-2-ol.	2004 Aug 5	15281774
Volatile composition and contribution to the aroma of spanish honeydew honeys. Identification of a new chemical marker.	2006 Jun 28	16787032
Purification and characterization of 2-aminoacetophenone reductase of newly isolated Burkholderia sp. YT.	2007 Nov	18086443
3-(2-Acetyl-anilino)propanoic acid.	2008 Nov 13	21581332
Silica gel-catalyzed one-pot syntheses in water and fluorescence properties studies of 5-amino-2-aryl-3H-chromeno[4,3,2-de][1,6]naphthyridine-4-carbonitriles and 5-amino-2-aryl-3H-quinolino[4,3,2-de][1,6]naphthyridine-4-carbonitriles.	2010 Jan-Feb	20025233
N-[2-(4-Methyl-2-quinol-yl)phen-yl]acetamide: a P1 structure with Z = 4.	2010 Jul 17	21588351
(E)-N-{2-[1-(Benzyl-imino)eth-yl]phen-yl}benzamide.	2010 Mar 3	21580590

Patents

Substance Class	Chemical Created by `admin` on `Sat Dec 16 04:19:00 GMT 2023` Edited by `admin` on `Sat Dec 16 04:19:00 GMT 2023`
Record UNII	4M571C83H7
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

PHENACYLAMINE

Systematic Name

English

.ALPHA.-DEMETHYLCATHINONE

Common Name

English

.OMEGA.-AMINOACETOPHENONE

Systematic Name

English

ACETOPHENONE, 2-AMINO-

Systematic Name

English

2-OXOPHENETHYLAMINE

Systematic Name

English

(2-OXO-2-PHENYLETHYL)AMINE

Systematic Name

English

2-OXO-2-PHENYLETHANAMINE

Systematic Name

English

1-PHENYL-2-AMINOETHANONE

Systematic Name

English

PHENACYLAMINE [MI]

Common Name

English

ACETOPHENONE, .ALPHA.-AMINO-

Systematic Name

English

2-AMINO-1-PHENYLETHANONE

Systematic Name

English

2-AMINOACETOPHENONE

Systematic Name

English

.ALPHA.-AMINOACETOPHENONE

Systematic Name

English

Classification Tree Code System Code

JECFA EVALUATION

2-AMINOACETOPHENONE