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69257-51-8

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69257-51-8 Usage

Molecular weight

191.17 g/mol

Type of compound

Chemical compound

Derivative of

Glucose

Common use

Substrate for the enzyme nitroaldose reductase

Potential applications

Pharmaceutical industry (antiviral and antibiotic medications)

Additional use

Research and laboratory settings as a reagent in organic synthesis

Physical appearance

White to off-white crystalline powder

Stability

Stable under normal conditions

Storage requirements

Cool, dry place away from direct sunlight and moisture

Check Digit Verification of cas no

The CAS Registry Mumber 69257-51-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,2,5 and 7 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 69257-51:
(7*6)+(6*9)+(5*2)+(4*5)+(3*7)+(2*5)+(1*1)=158
158 % 10 = 8
So 69257-51-8 is a valid CAS Registry Number.

69257-51-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-Desoxy-1-nitro-L-gluco-hexitol

1.2 Other means of identification

Product number -
Other names 1-nitro-1-deoxy-L-glucitol

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:69257-51-8 SDS

69257-51-8Relevant articles and documents

Larger laboratory scale synthesis of 5-methyluridine and formal synthesis of its L-enantiomer

Thiesen, Luciano J. Hoeltgebaum,Cabral, Nadia,Joselice E Silva, Maria,Bezerra, Gilson,Doboszewski, Bogdan

, p. 249 - 264 (2017/06/19)

A larger laboratory scale synthesis (>60 g per run) of 5-methyluridine is presented. The critical intermediate 1,2-O-isopropylidene-α-D-ribofuranose was prepared from very cheap D-glucose via D-allose. Its L-enantiomer was obtained from L-arabinose via L-glucose, and also from L-xylose. {figure presented}.

Synthesis of daunosamine

Grethe,Mitt,Williams,Uskokovic

, p. 5309 - 5315 (2007/10/02)

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