DIETHYL TARTRATE

Details

Stereochemistry	ABSOLUTE
Molecular Formula	C8H14O6
Molecular Weight	206.1932
Optical Activity	UNSPECIFIED
Defined Stereocenters	2 / 2
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure Search

SMILES

CCOC(=O)[C@H](O)[C@@H](O)C(=O)OCC

InChI

InChIKey=YSAVZVORKRDODB-PHDIDXHHSA-N

InChI=1S/C8H14O6/c1-3-13-7(11)5(9)6(10)8(12)14-4-2/h5-6,9-10H,3-4H2,1-2H3/t5-,6-/m1/s1

HIDE SMILES / InChI

Molecular Formula	C8H14O6
Molecular Weight	206.1932
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
First total synthesis of (-)-ichthyothereol and its acetate.	2001 Aug 24	11511265
First total synthesis of (-)-AL-2.	2003 Jun 26	12816442
Self-assembly of an unpolar enantiomerically pure helicate-type metalla-cryptand.	2003 Oct 21	14594263
Total synthesis of mycalamide A.	2005 May 25	15898759
Studies on panax acetylenes: absolute structure of a new panax acetylene, and inhibitory effects of related acetylenes on the growth of L-1210 cells.	2007 Apr	17409548
Stereoselective total syntheses of three Lycopodium alkaloids, (-)-magellanine, (+)-magellaninone, and (+)-paniculatine, based on two Pauson-Khand reactions.	2007 Dec 21	18044932
Spectroscopic investigation of the structures of dialkyl tartrates and their cyclodextrin complexes.	2007 Feb 8	17266226
Studies toward the asymmetric synthesis of the right part of the mycalamides.	2007 Jan 19	17221953
Separation of corticosteroids by microemulsion EKC with diethyl L-tartrate as the oil phase.	2007 Oct	17893939
Development of chiral terminal-alkene-phosphine hybrid ligands for palladium-catalyzed asymmetric allylic substitutions.	2010 Jul 2	20536224
A practical and azide-free synthetic approach to oseltamivir from diethyl D-tartrate.	2010 May 7	20394411
Manganese catalyzed cis-dihydroxylation of electron deficient alkenes with H(2)O(2).	2010 Oct 7	20714666
Enantioselective synthesis of the novel chiral sulfoxide derivative as a glycogen synthase kinase 3beta inhibitor.	2010 Sep	20823611

Patents

Substance Class	Chemical Created by `admin` on `Fri Dec 15 19:17:37 GMT 2023` Edited by `admin` on `Fri Dec 15 19:17:37 GMT 2023`
Record UNII	OQ72CPY58Z
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

DIETHYL TARTRATE

Systematic Name

English

DIETHYL (2R,3R)-(+)-TARTRATE

Common Name

English

DIETHYL (+)-TARTRATE

Systematic Name

English

BUTANEDIOIC ACID, 2,3-DIHYDROXY- (2R,3R)-, 1,4-DIETHYL ESTER

Common Name

English

BUTANEDIOIC ACID, 2,3-DIHYDROXY- (2R,3R)-, DIETHYL ESTER

Common Name

English

L-DIETHYL TARTRATE

Common Name

English

NSC-44808

Code

English

DIETHYL TARTRATE [MI]

Common Name

English

DIETHYL 1,2-DIHYDROXY-1,2-ETHANEDICARBOXYLATE

Systematic Name

English

BUTANEDIOIC ACID, 2,3-DIHYDROXY-(R-(R*,R*))-, DIETHYL ESTER

Common Name

English

DIETHYL L-TARTRATE

Systematic Name

English

TARTARIC ACID, DIETHYL ESTER

Common Name

English

FEMA NO. 2378

Code

English

DIETHYL (2R,3R)-2,3-DIHYDROXYSUCCINATE

Systematic Name

English

(R,R)-TARTARIC ACID DIETHYL ESTER

Systematic Name

English

DIETHYL TARTRATE [FHFI]

Common Name

English

(+)-(R,R)-DIETHYL TARTRATE

Systematic Name

English

(R,R)-DIETHYL TARTRATE

Systematic Name

English

DIETHYL L-(+)-TARTRATE

Systematic Name

English

L-TARTARIC ACID DIETHYL ESTER

Systematic Name

English

Classification Tree Code System Code

JECFA EVALUATION

DIETHYL TARTRATE