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60903-54-0

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60903-54-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 60903-54-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,9,0 and 3 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 60903-54:
(7*6)+(6*0)+(5*9)+(4*0)+(3*3)+(2*5)+(1*4)=110
110 % 10 = 0
So 60903-54-0 is a valid CAS Registry Number.

60903-54-0SDS

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 1-[2-methyl-5-(phenylcarbamoylamino)phenyl]-3-phenylurea

1.2 Other means of identification

Product number -
Other names N',N'''-Diphenyl-N,N''-(4-methyl-m-phenylen)-di-harnstoff

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:60903-54-0 SDS

60903-54-0Downstream Products

60903-54-0Relevant articles and documents

Synthesis and antitussive activity of obtucarbamate A derivatives

Gan, Xiuhai,Liang, Zhiyuan,Ma, Xiaoyun,Wei, Gang,Zhou, Qingdi

, (2020/06/01)

Obtucarbamate A was purified from Disporum cantoniense with good antitussive property. In present work, a series of obtucarbamate A derivatives were designed and synthesized from obtucarbamate A by microwave method, and their antitussive activity were evaluated. The results showed that the toluene diisocyanate was obtained with a yield of 95.1percent using a simple method, 1-methyl-2-pyrrolidinone as solvent, temperature of 190 °C, microwave irradiation at 60 W power for 30 min. All compounds have good antitussive activity, and small steric hindrance unsaturated groups of ester chains and amino groups favor activity. It is the first reported of obtucarbamate A derivatives used as antitussive, and the results provide a basis for the application of obtucarbamate derivatives as new antitussive.

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