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Details

Stereochemistry ACHIRAL
Molecular Formula C14H14O2
Molecular Weight 214.2598
Optical Activity UNSPECIFIED
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of HYDROBENZOIN, MESO-

SMILES

O[C@@H]([C@@H](O)C1=CC=CC=C1)C2=CC=CC=C2

InChI

InChIKey=IHPDTPWNFBQHEB-OKILXGFUSA-N
InChI=1S/C14H14O2/c15-13(11-7-3-1-4-8-11)14(16)12-9-5-2-6-10-12/h1-10,13-16H/t13-,14+

HIDE SMILES / InChI

Molecular Formula C14H14O2
Molecular Weight 214.2598
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 2 / 2
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

PubMed

PubMed

TitleDatePubMed
Bidirectional metalation of hydrobenzoin: direct access to new chiral ligands and auxiliaries.
2009-05-07
Oxidative cleavage of hydrobenzoin by ACC/silica gel under ultrasound irradiation.
2009-01
Catalytic enantioselective allyl- and crotylboration of aldehydes using chiral diol x SnCl4 complexes. optimization, substrate scope and mechanistic investigations.
2008-07-02
Enantioselective oxidation of sulfides catalyzed by titanium complexes of 1,2-diarylethane-1,2-diols: effect of the aryl substitution.
2008-03
Production, properties and application to biocatalysis of a novel extracellular alkaline phenol oxidase from the thermophilic fungus Scytalidium thermophilum.
2006-08
A structural investigation of the N-B interaction in an o-(N,N-dialkylaminomethyl)arylboronate system.
2006-02-01
Migration behavior and enantioseparation of hydrobenzoin and structurally related compounds in capillary zone electrophoresis with a dual cyclodextrin system consisting of heptakis-(2,3-dihydroxy-6-O-sulfo)-beta-cyclodextrin and beta-cyclodextrin.
2005-11
Enantioseparations of hydrobenzoin and structurally related compounds in capillary zone electrophoresis using heptakis(2,3-dihydroxy-6-O-sulfo)-beta-cyclodextrin as chiral selector and enantiomer migration reversal of hydrobenzoin with a dual cyclodextrin system in the presence of borate complexation.
2004-08
Enantioseparation of benzoins and enantiomer migration reversal of hydrobenzoin in capillary zone electrophoresis with dual cyclodextrin systems and borate complexation.
2004-04-02
Comparative studies on the enantioseparation of hydrobenzoin and structurally related compounds by capillary zone electrophoresis with sulfated beta-cyclodextrin as the chiral selector in the presence and absence of borate complexation.
2004-04-02
Synthesis and characterization of carboxymethylated cyclosophoraose, and its inclusion complexation behavior.
2004-02-25
Asymmetric reduction of benzil to (S)-benzoin with whole cells of Bacillus cereus.
2003-12
Use of poly(sodium oleyl-L-leucylvalinate) surfactant for the separation of chiral compounds in micellar electrokinetic chromatography.
2003-09
Truly catalytic and enantioselective pinacol coupling of aryl aldehydes mediated by chiral Ti(III) complexes.
2003-07-11
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 22:58:30 GMT 2025
Edited
by admin
on Mon Mar 31 22:58:30 GMT 2025
Record UNII
CO9A49A84I
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ERYTHRO-HYDROBENZOIN
Preferred Name English
HYDROBENZOIN, MESO-
Common Name English
NSC-133570
Code English
MESO-1,2-DIPHENYLETHYLENE GLYCOL
Common Name English
MESO-STILBENE GLYCOL
Common Name English
MESO-HYDROBENZOIN
Common Name English
1,2-ETHANEDIOL, 1,2-DIPHENYL-, (1R,2S)-REL-
Systematic Name English
HYDROBENZOIN MESO-FORM [MI]
Common Name English
Code System Code Type Description
CHEBI
50015
Created by admin on Mon Mar 31 22:58:30 GMT 2025 , Edited by admin on Mon Mar 31 22:58:30 GMT 2025
PRIMARY
EPA CompTox
DTXSID701021446
Created by admin on Mon Mar 31 22:58:30 GMT 2025 , Edited by admin on Mon Mar 31 22:58:30 GMT 2025
PRIMARY
NSC
133570
Created by admin on Mon Mar 31 22:58:30 GMT 2025 , Edited by admin on Mon Mar 31 22:58:30 GMT 2025
PRIMARY
PUBCHEM
853018
Created by admin on Mon Mar 31 22:58:30 GMT 2025 , Edited by admin on Mon Mar 31 22:58:30 GMT 2025
PRIMARY
MERCK INDEX
m6085
Created by admin on Mon Mar 31 22:58:30 GMT 2025 , Edited by admin on Mon Mar 31 22:58:30 GMT 2025
PRIMARY Merck Index
CAS
579-43-1
Created by admin on Mon Mar 31 22:58:30 GMT 2025 , Edited by admin on Mon Mar 31 22:58:30 GMT 2025
PRIMARY
FDA UNII
CO9A49A84I
Created by admin on Mon Mar 31 22:58:30 GMT 2025 , Edited by admin on Mon Mar 31 22:58:30 GMT 2025
PRIMARY