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479035-71-7

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479035-71-7 Usage

Also known as

3,4-dihydroxytetrahydro-2H-pyran-2,5-dione

Class

Furandione derivatives

Uses

Production of resins and adhesives, cross-linking agent for polymers, manufacturing of pharmaceuticals, chemical intermediate in the synthesis of various organic compounds

Sustainable building block

Yes (due to renewable origin and versatile applications in multiple industries)

Check Digit Verification of cas no

The CAS Registry Mumber 479035-71-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,9,0,3 and 5 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 479035-71:
(8*4)+(7*7)+(6*9)+(5*0)+(4*3)+(3*5)+(2*7)+(1*1)=177
177 % 10 = 7
So 479035-71-7 is a valid CAS Registry Number.

479035-71-7SDS

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 bis(hydroxymethyl)maleic anhydride

1.2 Other means of identification

Product number -
Other names -

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:479035-71-7 SDS

479035-71-7Downstream Products

479035-71-7Relevant articles and documents

A new strategy for the synthesis of furan-3,4-dicarboxylic acid

Deshpande, Anil M.,Natu, Arvind A.,Argade, Narshinha P.

, p. 1010 - 1012 (2002)

A facile route to furan-3,4-dicarboxylic acid is described. Dimethylmaleic anhydride (1) on NBS-bromination followed by aqueous KOH treatment gave bis(hydroxymethyl)maleic anhydride (3), which on intramolecular Mitsunobu ring closure followed by esterification and DDQ-oxidation furnished the desired esters of furan-3,4-dicarboxylic acid 7a/b.

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