U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ACHIRAL
Molecular Formula C8H10O
Molecular Weight 122.1644
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of BENZYL METHYL ETHER

SMILES

COCC1=CC=CC=C1

InChI

InChIKey=GQKZBCPTCWJTAS-UHFFFAOYSA-N
InChI=1S/C8H10O/c1-9-7-8-5-3-2-4-6-8/h2-6H,7H2,1H3

HIDE SMILES / InChI

Approval Year

PubMed

PubMed

TitleDatePubMed
Chlorometabolite production by the ecologically important white rot fungus Bjerkandera adusta.
2001 Sep
The deprotonation of benzyl alcohol radical cations: a mechanistic dichotomy in the gas phase as in solution.
2002 Jan 18
Biradicals/zwitterions from thermolysis of enyne-isocyanates. Application to the synthesis of 2(1H)-pyridones, benzofuro[3,2-c]pyridin-1(2H)-ones, 2,5-dihydro-1H-pyrido[4,3-b]indol-1-ones, and related compounds.
2004 Jun 25
Synthesis and biological evaluation of phosphate prodrugs of 4-phospho-D-erythronohydroxamic acid, an inhibitor of 6-phosphogluconate dehydrogenase.
2007 Aug
Design, synthesis and SAR of potent statine-based BACE-1 inhibitors: exploration of P1 phenoxy and benzyloxy residues.
2008 Nov 1
6-methyl-2,4-disubstituted pyridazin-3(2H)-ones: a novel class of small-molecule agonists for formyl peptide receptors.
2009 Aug 27
Characterization of activity landscapes using 2D and 3D similarity methods: consensus activity cliffs.
2009 Feb
Structural elaboration of the surprising ortho-zincation of benzyl methyl ether.
2010 Apr 7
Dapdiamides, tripeptide antibiotics formed by unconventional amide ligases.
2010 Mar 26
Patents
Name Type Language
BENZYL METHYL ETHER
MI  
Systematic Name English
NSC-8058
Code English
1-(METHOXYMETHYL)BENZENE
Systematic Name English
(METHOXYMETHYL)BENZENE
Systematic Name English
.ALPHA.-METHOXYTOLUENE
Systematic Name English
METHYL BENZYL ETHER
Systematic Name English
BENZYL METHYL ETHER [MI]
Common Name English
Code System Code Type Description
ECHA (EC/EINECS)
208-705-7
Created by admin on Sat Dec 16 03:22:30 GMT 2023 , Edited by admin on Sat Dec 16 03:22:30 GMT 2023
PRIMARY
CAS
538-86-3
Created by admin on Sat Dec 16 03:22:30 GMT 2023 , Edited by admin on Sat Dec 16 03:22:30 GMT 2023
PRIMARY
EPA CompTox
DTXSID5060227
Created by admin on Sat Dec 16 03:22:30 GMT 2023 , Edited by admin on Sat Dec 16 03:22:30 GMT 2023
PRIMARY
PUBCHEM
10869
Created by admin on Sat Dec 16 03:22:30 GMT 2023 , Edited by admin on Sat Dec 16 03:22:30 GMT 2023
PRIMARY
NSC
8058
Created by admin on Sat Dec 16 03:22:30 GMT 2023 , Edited by admin on Sat Dec 16 03:22:30 GMT 2023
PRIMARY
FDA UNII
F22RLS78BD
Created by admin on Sat Dec 16 03:22:30 GMT 2023 , Edited by admin on Sat Dec 16 03:22:30 GMT 2023
PRIMARY
MERCK INDEX
m2413
Created by admin on Sat Dec 16 03:22:30 GMT 2023 , Edited by admin on Sat Dec 16 03:22:30 GMT 2023
PRIMARY Merck Index