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Details

Stereochemistry ACHIRAL
Molecular Formula C7H9NO
Molecular Weight 123.1525
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 4-HYDROXYBENZYLAMINE

SMILES

NCC1=CC=C(O)C=C1

InChI

InChIKey=RQJDUEKERVZLLU-UHFFFAOYSA-N
InChI=1S/C7H9NO/c8-5-6-1-3-7(9)4-2-6/h1-4,9H,5,8H2

HIDE SMILES / InChI

Molecular Formula C7H9NO
Molecular Weight 123.1525
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
(4-Hydroxy-phen-yl)methanaminium 2-(4-sulfanylphen-yl)acetate.
2009-09-05
Synthesis and biological evaluation of aminomethylphenol derivatives as inhibitors of the murine GABA transporters mGAT1-mGAT4.
2008-11
Inhibition of GABA shunt enzymes' activity by 4-hydroxybenzaldehyde derivatives.
2006-02
Inactivation of mitochondrial monoamine oxidase B by methylthio-substituted benzylamines.
2003-10-01
Fragmentation mechanisms of protonated benzylamines. Electrospray ionisation-tandem mass spectrometry study and ab initio molecular orbital calculations.
2003
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:58:54 GMT 2025
Edited
by admin
on Mon Mar 31 19:58:54 GMT 2025
Record UNII
7J7F85B7BI
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NSC-125720
Preferred Name English
4-HYDROXYBENZYLAMINE
Systematic Name English
4-HYDROXYBENZENEMETHANAMINE
Systematic Name English
P-CRESOL, .ALPHA.-AMINO-
Common Name English
P-HYDROXYBENZENEMETHANAMINE
Common Name English
P-(AMINOMETHYL)PHENO
Common Name English
(4-HYDROXYPHENYL)METHANAMINE
Systematic Name English
PHENOL, 4-(AMINOMETHYL)-
Systematic Name English
P-HYDROXYBENZYLAMINE
Common Name English
((4-HYDROXYPHENYL)METHYL)AMINE
Systematic Name English
Code System Code Type Description
CAS
696-60-6
Created by admin on Mon Mar 31 19:58:54 GMT 2025 , Edited by admin on Mon Mar 31 19:58:54 GMT 2025
PRIMARY
MESH
C048829
Created by admin on Mon Mar 31 19:58:54 GMT 2025 , Edited by admin on Mon Mar 31 19:58:54 GMT 2025
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PUBCHEM
97472
Created by admin on Mon Mar 31 19:58:54 GMT 2025 , Edited by admin on Mon Mar 31 19:58:54 GMT 2025
PRIMARY
EPA CompTox
DTXSID00219872
Created by admin on Mon Mar 31 19:58:54 GMT 2025 , Edited by admin on Mon Mar 31 19:58:54 GMT 2025
PRIMARY
NSC
125720
Created by admin on Mon Mar 31 19:58:54 GMT 2025 , Edited by admin on Mon Mar 31 19:58:54 GMT 2025
PRIMARY
FDA UNII
7J7F85B7BI
Created by admin on Mon Mar 31 19:58:54 GMT 2025 , Edited by admin on Mon Mar 31 19:58:54 GMT 2025
PRIMARY