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Details

Stereochemistry ACHIRAL
Molecular Formula C15H13NO2
Molecular Weight 239.2692
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of N-2-(7-HYDROXY-2-FLUORENYL)ACETAMIDE

SMILES

CC(=O)NC1=CC=C2C(CC3=CC(O)=CC=C23)=C1

InChI

InChIKey=RAYOKTUAMJNEFH-UHFFFAOYSA-N
InChI=1S/C15H13NO2/c1-9(17)16-12-2-4-14-10(7-12)6-11-8-13(18)3-5-15(11)14/h2-5,7-8,18H,6H2,1H3,(H,16,17)

HIDE SMILES / InChI

Molecular Formula C15H13NO2
Molecular Weight 239.2692
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Substance Class Chemical
Created
by admin
on Mon Mar 31 19:23:35 GMT 2025
Edited
by admin
on Mon Mar 31 19:23:35 GMT 2025
Record UNII
VGD8AM5AGN
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
N-2-(7-HYDROXY-2-FLUORENYL)ACETAMIDE
Common Name English
NSC-40566
Preferred Name English
7-HYDROXY-N-2-FLUORENYLACETAMIDE
Systematic Name English
ACETAMIDE, N-(7-HYDROXY-9H-FLUOREN-2-YL)-
Systematic Name English
N-(7-HYDROXY-2-FLUORENYL)ACETAMIDE
Systematic Name English
7-HYDROXY-2-ACETAMIDOFLUORENE
Systematic Name English
N-(7-HYDROXY-9H-FLUOREN-2-YL)ACETAMIDE
Systematic Name English
HYDROXY-2-ACETYLAMINOFLUORENE, 7-
Systematic Name English
7OH-2AAF
Common Name English
ACETAMIDE, N-(7-HYDROXYFLUOREN-2-YL)-
Systematic Name English
Code System Code Type Description
EPA CompTox
DTXSID30189837
Created by admin on Mon Mar 31 19:23:35 GMT 2025 , Edited by admin on Mon Mar 31 19:23:35 GMT 2025
PRIMARY
FDA UNII
VGD8AM5AGN
Created by admin on Mon Mar 31 19:23:35 GMT 2025 , Edited by admin on Mon Mar 31 19:23:35 GMT 2025
PRIMARY
CAS
363-49-5
Created by admin on Mon Mar 31 19:23:35 GMT 2025 , Edited by admin on Mon Mar 31 19:23:35 GMT 2025
PRIMARY
NSC
40566
Created by admin on Mon Mar 31 19:23:35 GMT 2025 , Edited by admin on Mon Mar 31 19:23:35 GMT 2025
PRIMARY
PUBCHEM
9695
Created by admin on Mon Mar 31 19:23:35 GMT 2025 , Edited by admin on Mon Mar 31 19:23:35 GMT 2025
PRIMARY