ChemicalBook--->CAS DataBase List--->7658-10-8

7658-10-8

7658-10-8 Structure

7658-10-8 Structure
IdentificationBack Directory
[Name]

6-Deoxy-L-talose
[CAS]

7658-10-8
[Synonyms]

L-6dTal
6-deoxytalose
L-Talomethylose
L-Talose, 6-deoxy-
[Molecular Formula]

C6H12O5
[MDL Number]

MFCD00269966
[MOL File]

7658-10-8.mol
[Molecular Weight]

164.16
Chemical PropertiesBack Directory
[Melting point ]

123-124°C
[storage temp. ]

Hygroscopic, -20°C Freezer, Under Inert Atmosphere
[solubility ]

DMF: 10mg/mL; DMSO: 20mg/mL; PBS (pH 7.2): 10mg/mL
[form ]

A solid
Hazard InformationBack Directory
[Description]

6-deoxy-L-Talose is a microbial monosaccharide that has been found in the cell wall of bacteria such as S. bovis and in the O-specific polysaccharide of LPS in species including E. coli and P. maltophilia. It is also a component of the surface glycopeptidolipids of M. avium.
[Chemical Properties]

White to Off-White Solid
[Uses]

6-Deoxy-L-talose (cas# 7658-10-8) is a compound useful in organic synthesis.
[Definition]

ChEBI: 6-deoxy-L-talose is an organic molecular entity.
[References]

[1] JOHN H. PAZUR. Glycans from streptococcal cell walls: An antigenic triheteroglycan of 6-deoxy-l-talose, l-rhamnose and d-galactose from Streptococcus bovis[J]. Archives of biochemistry and biophysics, 1972, 150 2: Pages 382-391. DOI: 10.1016/0003-9861(72)90053-7
[2] BARBARA JANN . NMR investigation of the 6-deoxy-l-talose-containing O45, O45-related (O45rel), and O66 polysaccharides of Escherichia coli[J]. Carbohydrate Research, 1995, 278 1: Pages 155-165. DOI: 10.1016/0008-6215(95)00243-6
[3] STEPHEN G. WILKINSON  W. J A  Lesley Galbraith. Lipopolysaccharides from Pseudomonas maltophilia: Composition of the lipopolysaccharide and structure of the side-chain polysaccharide from strain N.C.I.B. 9204[J]. Carbohydrate Research, 1983, 112 2: Pages 241-252. DOI: 10.1016/0008-6215(83)88289-5
[4] LINDSAY SWEET. Mycobacterium avium glycopeptidolipids require specific acetylation and methylation patterns for signaling through toll-like receptor 2.[J]. The Journal of Biological Chemistry, 2008, 283 48: 33221-33231. DOI: 10.1074/jbc.m805539200
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