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94815-09-5

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94815-09-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 94815-09-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,8,1 and 5 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 94815-09:
(7*9)+(6*4)+(5*8)+(4*1)+(3*5)+(2*0)+(1*9)=155
155 % 10 = 5
So 94815-09-5 is a valid CAS Registry Number.

94815-09-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N-((2-Phthalimidoyl-oxycarbonyl)-phenyl)-carbamidsaeureethylester

1.2 Other means of identification

Product number -
Other names N-[(2-Phthalimidoyl-oxycarbonyl)-phenyl]-carbamidsaeureethylester

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:94815-09-5 SDS

94815-09-5Relevant articles and documents

Cyanic Acid Ester. 35. On Formation and Consecutive Reactions of N-Cyanato Phthalimide. New Specifically Activated and Blocked Isatoic Acid Derivatives

Martin, Dieter,Nadolski, Karin,Gruendemann, Egon

, p. 737 - 746 (2007/10/02)

Depending on the reaction conditions N-hydroxy-phthalimide affords on treatment with cyanogen bromide via N-cyanato phthalimide 2 the iminocarbonate 3 and isatoic acid derivatives 7 and 16.Both the latter react with nucleophiles as isatoic acid derivatives activated on the carboxylic group and protected on the carbamic group or vice versa, furnishing N,N-bis alkoxycarbonyl anthranilic acid amides 9, N-alkoxycarbonyl anthranilic acid 12, o-alkoxycarbonyl phenyl ureas 17 and the benzotriazepin-2,5-dione 14.The structures of the new compounds are proved by 1H-n.m.r. and 13C-n.m.r. measurements as well as independent synthesis.

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