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2,4,6(1H,3H,5H)-Pyrimidinetrione, 1,3-bis(methoxymethyl)-5,5-diphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

97846-21-4

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97846-21-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 97846-21-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,8,4 and 6 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 97846-21:
(7*9)+(6*7)+(5*8)+(4*4)+(3*6)+(2*2)+(1*1)=184
184 % 10 = 4
So 97846-21-4 is a valid CAS Registry Number.

97846-21-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3-bis(methoxymethyl)-5,5-diphenyl-1,3-diazinane-2,4,6-trione

1.2 Other means of identification

Product number -
Other names 2,4,6(1H,3H,5h)-Pyrimidinetrione,1,3-bis(methoxymethyl)-5,5-diphenyl

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:97846-21-4 SDS

97846-21-4Relevant academic research and scientific papers

Method and reagents for N-alkylating ureides

-

, (2008/06/13)

A method of N-alkoxyalkylating ureides according to the invention comprises reacting a ureide of structure I with an alkylating agent of structure III in the presence of a basic catalyst in an aprotic reaction medium. The ureide may be a 5,5-disubstituted

Method of making barbituric acid derivatives

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, (2008/06/13)

There is disclosed an improved process for the preparation of 1,3-bis(alkoxyalkyl)- and 1,3-bis(benzyloxyalkyl)-5,5-disubstituted barbituric acid derivatives, such as 1,3-bis(methoxymethyl)phenobarbital, by reacting e.g., phenobarbital, preferably, a multiple molar excess of dimethoxymethane and an at least equimolar amount of anhydrous stannic chloride based on the amount of phenobarbital.

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