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Merck
CN

384313

(+)-Dimethyl 2,3-O-isopropylidene-D-tartrate

98%

Synonym(s):

(4S,5S)-2,2-Dimethyl-1,3-dioxolane-4,5-dicarboxylic acid dimethyl ester, Dimethyl (4S,5S)-2,2-dimethyl-1,3-dioxolane-4,5-dicarboxylate

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About This Item

Empirical Formula (Hill Notation):
C9H14O6
CAS Number:
Molecular Weight:
218.20
UNSPSC Code:
12352005
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
3548490
Assay:
98%
Form:
liquid
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Quality Segment

assay

98%

form

liquid

optical activity

[α]20/D +54°, neat

refractive index

n20/D 1.439 (lit.)

bp

80-82 °C/0.1 mmHg (lit.)

density

1.19 g/mL at 25 °C (lit.)

functional group

ester, ether, ketal

SMILES string

COC(=O)[C@H]1OC(C)(C)O[C@@H]1C(=O)OC

InChI

1S/C9H14O6/c1-9(2)14-5(7(10)12-3)6(15-9)8(11)13-4/h5-6H,1-4H3/t5-,6-/m0/s1

InChI key

ROZOUYVVWUTPNG-WDSKDSINSA-N

General description

(+)-Dimethyl 2,3-O-isopropylidene-D-tartrate is a chiral reagent used in organic synthesis. It is prepared by the reaction-rectification process from D -tartrate, and 2,2-dimethoxypropane.{138]

Application

(+)-Dimethyl 2,3-O-isopropylidene-D-tartrate can be used as a starting material for the synthesis of:
  • Deuterated 1-deoxy-D-xylose.
  • C-terminal peptide -oxo-aldehydes using Fmoc solid-phase peptide synthesis methodology (SPPS).
  • Bis-Weinreb amide, a key intermediate for the preparation of myo-inositol analog via ring-closing metathesis.

Valuable building block for TADDOL chiral auxiliaries, dipyridine ligands, and threitols.


Storage Class

10 - Combustible liquids

wgk

WGK 3

flash_point_f

275.0 °F - closed cup

flash_point_c

135 °C - closed cup

ppe

Eyeshields, Gloves



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