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Details

Stereochemistry ACHIRAL
Molecular Formula C8H7NO
Molecular Weight 133.1473
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 4-HYDROXYBENZYL CYANIDE

SMILES

OC1=CC=C(CC#N)C=C1

InChI

InChIKey=AYKYOOPFBCOXSL-UHFFFAOYSA-N
InChI=1S/C8H7NO/c9-6-5-7-1-3-8(10)4-2-7/h1-4,10H,5H2

HIDE SMILES / InChI

Approval Year

PubMed

PubMed

TitleDatePubMed
Host plant-dependent metabolism of 4-hydroxybenzylglucosinolate in Pieris rapae: substrate specificity and effects of genetic modification and plant nitrile hydratase.
2007 Nov
A critical quantum chemical and experimental study of the potentiality of direct labeling of the CN group with [(99m)Tc(CO)(3)](+) or [(186/188)Re(CO)(3)](+) in CN containing biomolecules.
2008 Oct
Novel phenolic glycosides, adenophorasides A-E, from Adenophora roots.
2010 Jul
Design of group IIA secreted/synovial phospholipase A(2) inhibitors: an oxadiazolone derivative suppresses chondrocyte prostaglandin E(2) secretion.
2010 Jun 1
Patents
Name Type Language
4-HYDROXYBENZYL CYANIDE
Systematic Name English
4-HYDROXYBENZENEACETONITRILE
Systematic Name English
NSC-76080
Code English
Code System Code Type Description
EPA CompTox
DTXSID90161856
Created by admin on Fri Dec 15 18:40:43 GMT 2023 , Edited by admin on Fri Dec 15 18:40:43 GMT 2023
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NSC
76080
Created by admin on Fri Dec 15 18:40:43 GMT 2023 , Edited by admin on Fri Dec 15 18:40:43 GMT 2023
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CHEBI
16667
Created by admin on Fri Dec 15 18:40:43 GMT 2023 , Edited by admin on Fri Dec 15 18:40:43 GMT 2023
PRIMARY
ECHA (EC/EINECS)
238-046-0
Created by admin on Fri Dec 15 18:40:43 GMT 2023 , Edited by admin on Fri Dec 15 18:40:43 GMT 2023
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CAS
14191-95-8
Created by admin on Fri Dec 15 18:40:43 GMT 2023 , Edited by admin on Fri Dec 15 18:40:43 GMT 2023
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FDA UNII
18Q5J224RM
Created by admin on Fri Dec 15 18:40:43 GMT 2023 , Edited by admin on Fri Dec 15 18:40:43 GMT 2023
PRIMARY
PUBCHEM
26548
Created by admin on Fri Dec 15 18:40:43 GMT 2023 , Edited by admin on Fri Dec 15 18:40:43 GMT 2023
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