Home Other Building Blocks (-)-Diethyl D-tartrate

(-)-Diethyl D-tartrate

CAS No.:
13811-71-7
Catalog Number:
AG0034OH
Molecular Formula:
C8H14O6
Molecular Weight:
206.1932
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
5g
98%
In Stock USA
United States
$13
- +
25g
98%
In Stock USA
United States
$19
- +
100g
98%
In Stock USA
United States
$57
- +
500g
98%
In Stock USA
United States
$188
- +
Product Description
Catalog Number:
AG0034OH
Chemical Name:
(-)-Diethyl D-tartrate
CAS Number:
13811-71-7
Molecular Formula:
C8H14O6
Molecular Weight:
206.1932
MDL Number:
MFCD00064451
IUPAC Name:
diethyl (2S,3S)-2,3-dihydroxybutanedioate
InChI:
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-/m0/s1
InChI Key:
YSAVZVORKRDODB-WDSKDSINSA-N
SMILES:
CCOC(=O)[C@H]([C@@H](C(=O)OCC)O)O
EC Number:
237-458-8
Properties
Complexity:
180  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
2  
Defined Bond Stereocenter Count:
0
Exact Mass:
206.079g/mol
Formal Charge:
0
Heavy Atom Count:
14  
Hydrogen Bond Acceptor Count:
6  
Hydrogen Bond Donor Count:
2  
Isotope Atom Count:
0
Molecular Weight:
206.194g/mol
Monoisotopic Mass:
206.079g/mol
Rotatable Bond Count:
7  
Topological Polar Surface Area:
93.1A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
-0.3  
Literature
Title Journal
Bioplastics from feather quill. Biomacromolecules 20111010
Biosynthetic chlorination of the piperazate residue in kutzneride biosynthesis by KthP. Biochemistry 20110712
Total synthesis of broussonetine F: the orthoamide Overman rearrangement of an allylic diol. Organic letters 20110218
A practical and azide-free synthetic approach to oseltamivir from diethyl D-tartrate. The Journal of organic chemistry 20100507
Effect of microemulsion component purity on the chromatographic figures of merit in chiral microemulsion electrokinetic chromatography. Journal of chromatography. A 20090417
Direct chlorination of alcohols with chlorodimethylsilane catalyzed by a gallium trichloride/tartrate system under neutral conditions. Organic & biomolecular chemistry 20080807
Use of large-scale chromatography in the preparation of armodafinil. Chirality 20080801
Natural products as an inspiration in the diversity-oriented synthesis of bioactive compound libraries. Natural product reports 20080801
Synthesis and characterization of mesoporous silica modified with chiral auxiliaries for their potential application as chiral stationary phase. Journal of chromatography. A 20080516
Separation of corticosteroids by microemulsion EKC with diethyl L-tartrate as the oil phase. Electrophoresis 20071001
Two-chiral component microemulsion EKC - chiral surfactant and chiral oil. Part 2: diethyl tartrate. Electrophoresis 20070801
Influence of microemulsion chirality on chromatographic figures of merit in EKC: results with novel three-chiral-component microemulsions and comparison with one- and two-chiral-component microemulsions. Electrophoresis 20070801
Spectroscopic investigation of the structures of dialkyl tartrates and their cyclodextrin complexes. The journal of physical chemistry. A 20070208
Synthesis and characterization of (S)-amino alcohol modified M41S as effective material for the enantioseparation of racemic compounds. Journal of chromatography. A 20061201
Total synthesis of the light-harvesting carotenoid peridinin. Angewandte Chemie (International ed. in English) 20060612
Total syntheses of naturally occurring diacetylenic spiroacetal enol ethers. The Journal of organic chemistry 20050722
Bifunctional nanocrystalline MgO for chiral epoxy ketones via Claisen-Schmidt condensation-asymmetric epoxidation reactions. Journal of the American Chemical Society 20040324
Synthesis and biological characterization of 1alpha,24,25-trihydroxy-2beta-(3-hydroxypropoxy)vitamin D(3) (24-hydroxylated ED-71). Steroids 20010101
Properties