Skip to Content
MilliporeSigma
All Photos(1)

Key Documents

38406

Sigma-Aldrich

1,2:3,4-Di-O-isopropylidene-α-D-galactopyranose

purum, ≥97.0% (sum of enantiomers, GC)

Synonym(s):

1,2:3,4-Di-O-isopropylidene-D-galactopyranose

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C12H20O6
CAS Number:
Molecular Weight:
260.28
Beilstein/REAXYS Number:
1345410
EC Number:
MDL number:
UNSPSC Code:
12352200
PubChem Substance ID:

grade

purum

assay

≥97.0% (sum of enantiomers, GC)

optical activity

[α]20/D −59±1°, c = 3% in chloroform

refractive index

n20/D 1.466 (lit.)

bp

117 °C/0.015 mmHg (lit.)

density

1.143 g/mL at 25 °C (lit.)

storage temp.

2-8°C

SMILES string

CC1(C)O[C@H]2O[C@H](CO)[C@@H]3OC(C)(C)O[C@@H]3[C@H]2O1

InChI

1S/C12H20O6/c1-11(2)15-7-6(5-13)14-10-9(8(7)16-11)17-12(3,4)18-10/h6-10,13H,5H2,1-4H3/t6-,7+,8+,9-,10-/m1/s1

InChI key

POORJMIIHXHXAV-SOYHJAILSA-N

Looking for similar products? Visit Product Comparison Guide

Other Notes

Chiral building block[1][2][3]

Storage Class

12 - Non Combustible Liquids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves


Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

It looks like we've run into a problem, but you can still download Certificates of Analysis from our Documents section.

If you need assistance, please contact Customer Support.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Stephen Hanessian et al.
The Journal of organic chemistry, 62(3), 465-473 (1997-02-07)
A highly stereocontrolled synthesis of ring D/E precursor to reserpine has been developed starting from (-)-quinic acid as a chiral template. The total synthesis of (-)-reserpine is described through the cyclization of an immonium lactam intermediate.
H.B. Mereyala et al.
Tetrahedron Letters, 32, 7317-7317 (1991)
J. Gervay et al.
The Journal of Organic Chemistry, 56, 5448-5448 (1991)

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service