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Details

Stereochemistry ACHIRAL
Molecular Formula C7H9N
Molecular Weight 107.1531
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of O-TOLUIDINE

SMILES

CC1=C(N)C=CC=C1

InChI

InChIKey=RNVCVTLRINQCPJ-UHFFFAOYSA-N
InChI=1S/C7H9N/c1-6-4-2-3-5-7(6)8/h2-5H,8H2,1H3

HIDE SMILES / InChI

Molecular Formula C7H9N
Molecular Weight 107.1531
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 Fri Dec 15 15:31:08 UTC 2023
Edited
by admin
on Fri Dec 15 15:31:08 UTC 2023
Record UNII
B635MZ0ZLU
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
O-TOLUIDINE
MI  
Common Name English
2-METHYLBENZENAMINE
Systematic Name English
O-METHYLBENZENAMINE
Common Name English
ORTHO-TOLUIDINE [IARC]
Common Name English
2-AMINOTOLUENE [HSDB]
Common Name English
O-METHYLANILINE
Common Name English
PRILOCAINE HYDROCHLORIDE IMPURITY B [EP IMPURITY]
Common Name English
O-TOLYLAMINE
Common Name English
O-AMINOTOLUENE
Common Name English
2-AMINOTOLUENE
HSDB  
Systematic Name English
2-METHYLPHENYLAMINE
Systematic Name English
PRILOCAINE RELATED COMPOUND A FREE BASE
Common Name English
2-AMINO-1-METHYLBENZENE
Systematic Name English
NSC-15348
Code English
1-AMINO-2-METHYLBENZENE
Systematic Name English
2-METHYL-1-AMINOBENZENE
Systematic Name English
O-TOLUIDINE [MI]
Common Name English
2-METHYLANILINE
Systematic Name English
PRILOCAINE IMPURITY B [EP IMPURITY]
Common Name English
2-TOLYLAMINE
Systematic Name English
BENZENAMINE, 2-METHYL-
Systematic Name English
Classification Tree Code System Code
NCI_THESAURUS C45178
Created by admin on Fri Dec 15 15:31:08 UTC 2023 , Edited by admin on Fri Dec 15 15:31:08 UTC 2023
Code System Code Type Description
CHEBI
66892
Created by admin on Fri Dec 15 15:31:08 UTC 2023 , Edited by admin on Fri Dec 15 15:31:08 UTC 2023
PRIMARY
WIKIPEDIA
o-Toluidine
Created by admin on Fri Dec 15 15:31:08 UTC 2023 , Edited by admin on Fri Dec 15 15:31:08 UTC 2023
PRIMARY
HSDB
2042
Created by admin on Fri Dec 15 15:31:08 UTC 2023 , Edited by admin on Fri Dec 15 15:31:08 UTC 2023
PRIMARY
ECHA (EC/EINECS)
202-429-0
Created by admin on Fri Dec 15 15:31:08 UTC 2023 , Edited by admin on Fri Dec 15 15:31:08 UTC 2023
PRIMARY
CAS
95-53-4
Created by admin on Fri Dec 15 15:31:08 UTC 2023 , Edited by admin on Fri Dec 15 15:31:08 UTC 2023
PRIMARY
EPA CompTox
DTXSID1026164
Created by admin on Fri Dec 15 15:31:08 UTC 2023 , Edited by admin on Fri Dec 15 15:31:08 UTC 2023
PRIMARY
MERCK INDEX
m10966
Created by admin on Fri Dec 15 15:31:08 UTC 2023 , Edited by admin on Fri Dec 15 15:31:08 UTC 2023
PRIMARY Merck Index
NCI_THESAURUS
C44429
Created by admin on Fri Dec 15 15:31:08 UTC 2023 , Edited by admin on Fri Dec 15 15:31:08 UTC 2023
PRIMARY
MESH
C023622
Created by admin on Fri Dec 15 15:31:08 UTC 2023 , Edited by admin on Fri Dec 15 15:31:08 UTC 2023
PRIMARY
FDA UNII
B635MZ0ZLU
Created by admin on Fri Dec 15 15:31:08 UTC 2023 , Edited by admin on Fri Dec 15 15:31:08 UTC 2023
PRIMARY
PUBCHEM
7242
Created by admin on Fri Dec 15 15:31:08 UTC 2023 , Edited by admin on Fri Dec 15 15:31:08 UTC 2023
PRIMARY
NSC
15348
Created by admin on Fri Dec 15 15:31:08 UTC 2023 , Edited by admin on Fri Dec 15 15:31:08 UTC 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
SALT/SOLVATE -> PARENT
Related Record Type Details
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
PARENT -> IMPURITY
CHROMATOGRAPHIC PURITY (TLC)
EP
Related Record Type Details
ACTIVE MOIETY