HYDROBENZOIN, (±)-

Details

Stereochemistry	RACEMIC
Molecular Formula	C14H14O2
Molecular Weight	214.2598
Optical Activity	( + / - )
Defined Stereocenters	2 / 2
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure Search

SMILES

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

InChI

InChIKey=IHPDTPWNFBQHEB-KBPBESRZSA-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-/m0/s1

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

Title	Date	PubMed
Synthesis of (+)-polyoxamic acid and D-sorbitol from simple achiral allylic halides employing (S,S)-hydrobenzoin as a chiral source.	2002-05-21	12122692
Chiral separation of enantiomeric 1,2-diamines using molecular imprinting method and selectivity enhancement by addition of achiral primary amines into eluents.	2002-01	11817724

Substance Class	Chemical Created by `admin` on `Mon Mar 31 22:42:52 GMT 2025` Edited by `admin` on `Mon Mar 31 22:42:52 GMT 2025`
Record UNII	UR8L8S2Y8M
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

HYDROBENZOIN, (±)-

Systematic Name

English

HYDROBENZOIN DL-FORM

Preferred Name

English

THREO-STILBENE GLYCOL

Common Name

English

DL-1,2-DIPHENYL-1,2-ETHANEDIOL

Common Name

English

HYDROBENZOIN DL-FORM [MI]

Common Name

English

1,2-ETHANEDIOL, 1,2-DIPHENYL-, (1S,2S)-REL-

Systematic Name

English

DL-HYDROBENZOIN

Common Name

English

ISOHYDROBENZOIN

Common Name

English

(±)-HYDROBENZOIN

Systematic Name

English

Code System Code Type Description

EPA CompTox

DTXSID801021449

Created by admin on Mon Mar 31 22:42:52 GMT 2025 , Edited by admin on Mon Mar 31 22:42:52 GMT 2025

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MERCK INDEX

m6085

Created by admin on Mon Mar 31 22:42:52 GMT 2025 , Edited by admin on Mon Mar 31 22:42:52 GMT 2025

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Merck Index

CAS

655-48-1

Created by admin on Mon Mar 31 22:42:52 GMT 2025 , Edited by admin on Mon Mar 31 22:42:52 GMT 2025

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FDA UNII

UR8L8S2Y8M

Created by admin on Mon Mar 31 22:42:52 GMT 2025 , Edited by admin on Mon Mar 31 22:42:52 GMT 2025

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