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39031-76-0

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39031-76-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 39031-76-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,0,3 and 1 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 39031-76:
(7*3)+(6*9)+(5*0)+(4*3)+(3*1)+(2*7)+(1*6)=110
110 % 10 = 0
So 39031-76-0 is a valid CAS Registry Number.

39031-76-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,4,5-trihydroxy-6-(4-nitrophenoxy)oxane-2-carboxylic acid

1.2 Other means of identification

Product number -
Other names 4-Nitrophenyl |A-D-galact-uronide

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:39031-76-0 SDS

39031-76-0Downstream Products

39031-76-0Relevant articles and documents

Preparation method of substituted benzyl or substituted phenyl beta-D-hexuronic acid glucoside

-

, (2018/10/19)

The invention relates to the technical field of pharmaceutical and chemical industries, and discloses a preparation method of substituted benzyl or substituted phenyl beta-D-hexuronic acid glucoside.The preparation method comprises the steps of taking hexuronic acid as a raw material, and performing acetylation, selective acyl removal, methyl esterification, bromization, aethrization and alkalinealcoholysis to form substituted benzyl or substituted phenyl beta-hexuronic acid glucoside with a structural formula as follows as shown in the description, wherein n is equal to 0-1; and R is o-, m-or para-hydrogen, nitryl, methoxy or halogen. The method is mild in reaction condition, simple in step and suitable for large-scale preparation, and a reaction reagent is easy to obtain.

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