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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
Asymmetric reduction of benzil to (S)-benzoin with whole cells of Bacillus cereus.
2003 Dec
Use of poly(sodium oleyl-L-leucylvalinate) surfactant for the separation of chiral compounds in micellar electrokinetic chromatography.
2003 Sep
Enantioseparation of benzoins and enantiomer migration reversal of hydrobenzoin in capillary zone electrophoresis with dual cyclodextrin systems and borate complexation.
2004 Apr 2
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 Apr 2
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 Aug
Synthesis and characterization of carboxymethylated cyclosophoraose, and its inclusion complexation behavior.
2004 Feb 25
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 Nov
Production, properties and application to biocatalysis of a novel extracellular alkaline phenol oxidase from the thermophilic fungus Scytalidium thermophilum.
2006 Aug
A structural investigation of the N-B interaction in an o-(N,N-dialkylaminomethyl)arylboronate system.
2006 Feb 1
Catalytic enantioselective allyl- and crotylboration of aldehydes using chiral diol x SnCl4 complexes. optimization, substrate scope and mechanistic investigations.
2008 Jul 2
Enantioselective oxidation of sulfides catalyzed by titanium complexes of 1,2-diarylethane-1,2-diols: effect of the aryl substitution.
2008 Mar
Oxidative cleavage of hydrobenzoin by ACC/silica gel under ultrasound irradiation.
2009 Jan
Bidirectional metalation of hydrobenzoin: direct access to new chiral ligands and auxiliaries.
2009 May 7
Patents
Substance Class Chemical
Created
by admin
on Sat Dec 16 10:01:22 GMT 2023
Edited
by admin
on Sat Dec 16 10:01:22 GMT 2023
Record UNII
CO9A49A84I
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
HYDROBENZOIN, MESO-
Common Name English
ERYTHRO-HYDROBENZOIN
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 Sat Dec 16 10:01:22 GMT 2023 , Edited by admin on Sat Dec 16 10:01:22 GMT 2023
PRIMARY
EPA CompTox
DTXSID701021446
Created by admin on Sat Dec 16 10:01:22 GMT 2023 , Edited by admin on Sat Dec 16 10:01:22 GMT 2023
PRIMARY
NSC
133570
Created by admin on Sat Dec 16 10:01:22 GMT 2023 , Edited by admin on Sat Dec 16 10:01:22 GMT 2023
PRIMARY
PUBCHEM
853018
Created by admin on Sat Dec 16 10:01:22 GMT 2023 , Edited by admin on Sat Dec 16 10:01:22 GMT 2023
PRIMARY
MERCK INDEX
m6085
Created by admin on Sat Dec 16 10:01:22 GMT 2023 , Edited by admin on Sat Dec 16 10:01:22 GMT 2023
PRIMARY Merck Index
CAS
579-43-1
Created by admin on Sat Dec 16 10:01:22 GMT 2023 , Edited by admin on Sat Dec 16 10:01:22 GMT 2023
PRIMARY
FDA UNII
CO9A49A84I
Created by admin on Sat Dec 16 10:01:22 GMT 2023 , Edited by admin on Sat Dec 16 10:01:22 GMT 2023
PRIMARY