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71573-09-6

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71573-09-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 71573-09-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,5,7 and 3 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 71573-09:
(7*7)+(6*1)+(5*5)+(4*7)+(3*3)+(2*0)+(1*9)=126
126 % 10 = 6
So 71573-09-6 is a valid CAS Registry Number.
InChI:InChI=1/C10H7NO4/c12-7-2-1-6(5-8(7)13)11-9(14)3-4-10(11)15/h1-5,12-13H

71573-09-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(3,4-dihydroxyphenyl) maleimide

1.2 Other means of identification

Product number -
Other names N-(3,4-dihydroxyphenyl)-maleimide

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:71573-09-6 SDS

71573-09-6Upstream product

71573-09-6Downstream Products

71573-09-6Relevant articles and documents

Process for the production of N-(hydroxyphenyl) maleimides

-

, (2008/06/13)

N-(hydroxyphenyl) maleimides of the general formula STR1 where R' stands for H, CH3, C2 H5, F, Cl, Br or I and n is an integer of 1-5 are produced by treating the corresponding maleamic acid or by treating the ester of said N-(hydroxyphenyl) maleimide at a temperature of 0-150° C. in the presence of at least one dehydrating agent selected from the group consisting of oxides and oxyacids of sulfur or phosphorus and alkali metal and alkaline earth metal salts of the said oxyacids. The corresponding maleamic acid can be obtained by reacting an aminophenol having one or more hydroxyl groups on its phenyl nucleus with maleic anhydride. The esters of the N-(hydroxyphenyl maleimide) can be obtained by reacting said aminophenol and said maleic anhydride in the presence of a conventional acid anhydride dehydrating agent and a conventional imide-forming cyclization catalyst.

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