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Details

Stereochemistry ACHIRAL
Molecular Formula C15H13NO
Molecular Weight 223.2698
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of N-3-FLUORENYLACETAMIDE

SMILES

CC(=O)NC1=CC=C2CC3=CC=CC=C3C2=C1

InChI

InChIKey=WIGMLEPKVNVQSQ-UHFFFAOYSA-N
InChI=1S/C15H13NO/c1-10(17)16-13-7-6-12-8-11-4-2-3-5-14(11)15(12)9-13/h2-7,9H,8H2,1H3,(H,16,17)

HIDE SMILES / InChI

Molecular Formula C15H13NO
Molecular Weight 223.2698
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Chromosomal localization of a unique gene by non-autoradiographic in situ hybridization.
1985-09-12
Effect of the structural isomer N-3-fluorenylacetamide on microsomal binding and hydroxylation of the carcinogen N-2-fluorenylacetamide.
1981-06-01
New 9-stubstituted 3-N,O-diacetylhydroxylaminofluorenes: enhanced electrophilicity and mutagenicity. Derivatives of fluorene. 38.
1980-03
Sensitivity of the conformation of deoxyguanosine to binding at the C-8 position by N-acetylated and unacetylated 2-aminofluorene.
1980
Microsomal metabolism of arylamides by the rat and guinea pig--I. Oxidation of N-3-fluorenylacetamide at carbon-atom-9--a major metabolic reaction.
1978
Separation and identification of metabolites of the arylamide, N-3-fluorenyl-acetamide, by high-pressure liquid chromatography.
1977-11-21
Mammary carcinogenesis in the rat by topical application of fluorenylhydroxamic acids and their acetates.
1977-01
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:53:01 GMT 2025
Edited
by admin
on Mon Mar 31 18:53:01 GMT 2025
Record UNII
4P9MD74D4T
Record Status Validated (UNII)
Record Version
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Name Type Language
N-3-FLUORENYLACETAMIDE
Systematic Name English
NSC-9865
Preferred Name English
N-ACETYL-3-AMINOFLUORENE
Systematic Name English
3-ACETYLAMINOFLUORENE
Systematic Name English
ACETAMIDE, N-FLUOREN-3-YL-
Systematic Name English
ACETAMIDE, N-9H-FLUOREN-3-YL-
Systematic Name English
Code System Code Type Description
PUBCHEM
22722
Created by admin on Mon Mar 31 18:53:01 GMT 2025 , Edited by admin on Mon Mar 31 18:53:01 GMT 2025
PRIMARY
EPA CompTox
DTXSID40212125
Created by admin on Mon Mar 31 18:53:01 GMT 2025 , Edited by admin on Mon Mar 31 18:53:01 GMT 2025
PRIMARY
NSC
9865
Created by admin on Mon Mar 31 18:53:01 GMT 2025 , Edited by admin on Mon Mar 31 18:53:01 GMT 2025
PRIMARY
MESH
C100047
Created by admin on Mon Mar 31 18:53:01 GMT 2025 , Edited by admin on Mon Mar 31 18:53:01 GMT 2025
PRIMARY
FDA UNII
4P9MD74D4T
Created by admin on Mon Mar 31 18:53:01 GMT 2025 , Edited by admin on Mon Mar 31 18:53:01 GMT 2025
PRIMARY
CAS
6292-55-3
Created by admin on Mon Mar 31 18:53:01 GMT 2025 , Edited by admin on Mon Mar 31 18:53:01 GMT 2025
PRIMARY