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Details

Stereochemistry ACHIRAL
Molecular Formula C13H13N
Molecular Weight 183.249
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of BENZYLANILINE

SMILES

C(NC1=CC=CC=C1)C2=CC=CC=C2

InChI

InChIKey=GTWJETSWSUWSEJ-UHFFFAOYSA-N
InChI=1S/C13H13N/c1-3-7-12(8-4-1)11-14-13-9-5-2-6-10-13/h1-10,14H,11H2

HIDE SMILES / InChI

Molecular Formula C13H13N
Molecular Weight 183.249
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Redetermination of 1-benzyl-3-furoyl-1-phenyl-thio-urea.
2009-02-28
Synthesis, characterization and catalytic activity of saturated and unsaturated N-heterocyclic carbene iridium(i) complexes.
2009-02-07
Anti-microtubule activity of tubeimoside I and its colchicine binding site of tubulin.
2008-09
de novo design and synthesis of N-benzylanilines as new candidates for VEGFR tyrosine kinase inhibitors.
2008-03-21
Optically sensed, molecular shuttles driven by acid-base chemistry.
2007-12-07
Copper-catalyzed amidation of sp3 C-H bonds adjacent to a nitrogen atom.
2007-09-13
Optical properties of the poly(N-benzylaniline) thin film.
2006-01-12
[2]pseudorotaxane formation with N-benzylanilinium axles and 24-crown-8 ether wheels.
2005-10-27
N-benzylideneaniline and N-benzylaniline are potent inhibitors of lignostilbene-alpha,beta-dioxygenase, a key enzyme in oxidative cleavage of the central double bond of lignostilbene.
2003-06
Synthesis, anticancer activity, and inhibition of tubulin polymerization by conformationally restricted analogues of lavendustin A.
2003-04-24
A new pathway for hydroamination. Mechanism of palladium-catalyzed addition of anilines to vinylarenes.
2002-02-20
Antidepressant activity of aspartic acid derivatives.
2001-04
Substance Class Chemical
Created
by admin
on Mon Mar 31 21:20:47 GMT 2025
Edited
by admin
on Mon Mar 31 21:20:47 GMT 2025
Record UNII
R1FVH9A316
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NSC-147284
Preferred Name English
BENZYLANILINE
MI  
Systematic Name English
BENZENAMINE, N-(PHENYLMETHYL)-
Systematic Name English
PHENYLBENZYLAMINE
Systematic Name English
BENZYLPHENYLAMINE
Systematic Name English
N-PHENYLBENZYLAMINE
Systematic Name English
N-PHENYL-N-BENZYLAMINE
Systematic Name English
N-PHENYLBENZENEMETHANAMINE
Systematic Name English
N-BENZYLPHENYLAMINE
Systematic Name English
BENZYLAMINE, N-PHENYL-
Systematic Name English
N-BENZYL-N-PHENYLAMINE
Systematic Name English
N-BENZYLBENZENAMINE
Systematic Name English
BENZYLANILINE [MI]
Common Name English
N-BENZYLANILINE
Systematic Name English
Code System Code Type Description
MERCK INDEX
m2399
Created by admin on Mon Mar 31 21:20:48 GMT 2025 , Edited by admin on Mon Mar 31 21:20:48 GMT 2025
PRIMARY Merck Index
ECHA (EC/EINECS)
203-100-4
Created by admin on Mon Mar 31 21:20:48 GMT 2025 , Edited by admin on Mon Mar 31 21:20:48 GMT 2025
PRIMARY
NSC
147284
Created by admin on Mon Mar 31 21:20:48 GMT 2025 , Edited by admin on Mon Mar 31 21:20:48 GMT 2025
PRIMARY
CAS
103-32-2
Created by admin on Mon Mar 31 21:20:48 GMT 2025 , Edited by admin on Mon Mar 31 21:20:48 GMT 2025
PRIMARY
EPA CompTox
DTXSID7059272
Created by admin on Mon Mar 31 21:20:48 GMT 2025 , Edited by admin on Mon Mar 31 21:20:48 GMT 2025
PRIMARY
PUBCHEM
66028
Created by admin on Mon Mar 31 21:20:48 GMT 2025 , Edited by admin on Mon Mar 31 21:20:48 GMT 2025
PRIMARY
FDA UNII
R1FVH9A316
Created by admin on Mon Mar 31 21:20:48 GMT 2025 , Edited by admin on Mon Mar 31 21:20:48 GMT 2025
PRIMARY
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