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83560-86-5

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83560-86-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 83560-86-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,5,6 and 0 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 83560-86:
(7*8)+(6*3)+(5*5)+(4*6)+(3*0)+(2*8)+(1*6)=145
145 % 10 = 5
So 83560-86-5 is a valid CAS Registry Number.
InChI:InChI=1/C15H14N2O5/c1-8-9(2)15(22)17(14(8)21)11-5-3-10(4-6-11)13(20)16-7-12(18)19/h3-6H,7H2,1-2H3,(H,16,20)(H,18,19)

83560-86-5SDS

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 2-[[4-(3,4-dimethyl-2,5-dioxopyrrol-1-yl)benzoyl]amino]acetic acid

1.2 Other means of identification

Product number -
Other names DMMHA

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:83560-86-5 SDS

83560-86-5Downstream Products

83560-86-5Relevant articles and documents

Synthesis and spectroscopic evidences of N-arylmaleimides and N-aryl-2,3-dimethylmaleimides

Fles, Dragutin,Vukovic, Radivoje,Kuzmic, Ana Erceg,Bogdanic, Grozdana,Pilizota, Vlasta,Karlovic, Damir,Markus, Kresimir,Wolsperger, Kristina,Vikic-Topic, Drazen

, p. 69 - 74 (2007/10/03)

A series of N-arylmaleimides (N-aryl-MI) and N-aryl-2,3-dimethylmaleimides (N-aryl-DiMeMI) were prepared by condensation of primary amines with maleic anhydride (MAn) and 2,3-dimethylmaleic anhydride (DiMeMAn), respectively. Preparation of N-aryl-MI proceeded through the formation of N-arylmaleamic acid, which subsequently cyclized to N-aryl-MI. In the reaction of N-arylamines with DiMeMAn, cyclic condensation products were formed in one step. By means of one- and two-dimensional 1H and 13C NMR spectroscopy it was proven that N-aryl-DiMeMI and not isomaleimides were formed by a one step reaction.

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