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58936-19-9

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58936-19-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 58936-19-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,9,3 and 6 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 58936-19:
(7*5)+(6*8)+(5*9)+(4*3)+(3*6)+(2*1)+(1*9)=169
169 % 10 = 9
So 58936-19-9 is a valid CAS Registry Number.

58936-19-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name benzyl N-maleimidyl carbonate

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:58936-19-9 SDS

58936-19-9Downstream Products

58936-19-9Relevant articles and documents

Synthesis of N-Hydroxymaleimide and N-Hydroxyitaconimide and their Related Derivatives

Akiyama, Masayasu,Shimizu, Kazuyuki,Aiba, Seiichi,Banba, Fumio

, p. 2122 - 2125 (2007/10/02)

Thermolysis of alkyl and aryl carbonates of N-hydroxy-3,6-epoxy-1,2,3,6-tetrahydrophthalimide yielded the corresponding alkyl or aryl N-maleimidyl carbonates.The benzyl or phenyl carbonate afforded N-hydroxymaleimide, either by treatment with trifluoroacetic acid or by refluxing in methanol.N-hydroxyitaconimide was obtained by dehydration of N-hydroxyitaconamic acid with dicyclohexylcarbodi-imide (DCC).The DCC dehydration of N-acetoxy- and N-benzyloxy-itaconamic acids produced iminofuranones, which could be rearranged to imides.Deacylation of N-acetoxymaleimide was unsuccessful, whereas aminolysis of N-acetoxyitaconimide yielded the N-hydroxyimide.

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