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1-Cyano-3-phenylurea is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

41834-91-7

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41834-91-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 41834-91-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,8,3 and 4 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 41834-91:
(7*4)+(6*1)+(5*8)+(4*3)+(3*4)+(2*9)+(1*1)=117
117 % 10 = 7
So 41834-91-7 is a valid CAS Registry Number.

41834-91-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-cyano-3-phenylurea

1.2 Other means of identification

Product number -
Other names Phenylcarbamincyanid

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:41834-91-7 SDS

41834-91-7Relevant academic research and scientific papers

Production of 1-phenyl-3-cyanoureas

-

, (2008/06/13)

Disclosed herein is a method for producing 1-phenyl-3-cyanoureas with the general formula: STR1 by reacting the corresponding benzamide with an alkali metal or alkaline earth metal hypohalite followed by reaction with cyanamide.

Process for preparing quinazolines

-

, (2008/06/13)

2-Halo-4-aminoquinazolines are produced by a two-step process involving cyclization of 1-phenyl-3-cyanoureas or 1-phenyl-3-cyanothioureas in the presence of phosphorus halides and phosphorus oxyhalides to provide a phosphoquinazoline intermediate which is hydrolyzed to the quinazoline. Exemplary of the process is the intramolecular cyclization of 1-(3,4-dimethoxyphenyl)-3-cyanourea in the presence of phosphorus pentachloride and phosphorus oxychloride to a phosphoquinazoline intermediate which is subsequently hydrolyzed with formic acid to 2-chloro-4-amino-6,7-dimethoxy-quinazoline. The 2-halo-4-aminoquinazolines of the instant process are particularly valuable as intermediates in the preparation of 4-amino-2-(4-substituted-piperazin-l-yl)quinazolines useful in the treatment of cardiovascular disease, e.g. hypertension.

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