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5-Deoxy-D-lyxose is a monosaccharide, a type of sugar molecule, that is derived from L-Fucose, which is isolated from seaweed. It plays a significant role in various biological processes and has potential applications in different industries due to its unique chemical properties.

49694-62-4

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49694-62-4 Usage

Uses

Used in Pharmaceutical Industry:
5-Deoxy-D-lyxose is used as an intermediate in the synthesis of various pharmaceutical compounds. Its ability to be derived from L-Fucose, a naturally occurring substance, makes it a valuable component in the development of new drugs and therapies.
Used in Chemical Synthesis:
5-Deoxy-D-lyxose is used as a key component in the synthesis of Neopatulin, a naturally occurring compound with potential applications in various fields. Its role in the synthesis process highlights its importance in the creation of new and innovative products.

Check Digit Verification of cas no

The CAS Registry Mumber 49694-62-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,9,6,9 and 4 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 49694-62:
(7*4)+(6*9)+(5*6)+(4*9)+(3*4)+(2*6)+(1*2)=174
174 % 10 = 4
So 49694-62-4 is a valid CAS Registry Number.

49694-62-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name D-5-deoxy-lyxose

1.2 Other means of identification

Product number -
Other names D-lyxomethylose

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:49694-62-4 SDS

49694-62-4Relevant academic research and scientific papers

SYNTHESIS AND N.M.R.-SPECTRAL ANALYSIS OF UNENRICHED AND -ENRICHED 5-DEOXYPENTOSES AND 5-O-METHYLPENTOSES

Snyder. Joseph R.,Serianni, Anthony S.

, p. 169 - 188 (2007/10/02)

Chemical methods are described for preparing unenriched and -enriched 5-deoxy- and 5-O-methyl-pentoses in the D or L configuration.The 1H-n.m.r.-spectra of these compounds have been interpreted, and the 13C n.m.r. spectra assigned with the aid of 2-D 13C-1H chemical-shift correlation spectroscopy.Tautomeric forms (furanoses, hydrate, and aldehyde) in solution in 2H2O have been quantified with the aid of -enriched derivatives.Spectra of 5-deoxypentoses, and methyl pentofuranosides have been compared, in order to assess the effect of 5-C-deoxygenation and 5-O-methylation on chemical shifts and coupling constants (1H-1H, 13C-1H, and 13C-13C) and on the pentofuranose conformations.

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