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N,N'-BIS(5-METHYLPYRIDIN-2-YL)UREA is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

63272-29-7

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63272-29-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 63272-29-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,2,7 and 2 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 63272-29:
(7*6)+(6*3)+(5*2)+(4*7)+(3*2)+(2*2)+(1*9)=117
117 % 10 = 7
So 63272-29-7 is a valid CAS Registry Number.

63272-29-7SDS

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 1,3-bis(5-methylpyridin-2-yl)urea

1.2 Other means of identification

Product number -
Other names Urea,N,N'-bis(5-methyl-2-pyridinyl)

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:63272-29-7 SDS

63272-29-7Downstream Products

63272-29-7Relevant academic research and scientific papers

Preparation method of substituted urea compound

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Paragraph 0066-0069; 0079, (2021/06/09)

The invention provides a preparation method of a substituted urea compound. The preparation method comprises the following steps: taking a nitrogen-containing heterocyclic compound and tetrahalomethane as raw materials, carrying out illumination catalytic reaction in the presence of a catalyst and a solvent to prepare the substituted urea compound and a halogen simple substance; the preparation method is wide in raw material source, phosgene, triphosgene and the like which are high in toxicity are prevented from being adopted as raw materials, the influence of the preparation process on the environment is reduced, and the atom utilization rate of the reaction is increased; the reaction conditions are mild, the operation is simple and convenient, the environmental pollution is reduced, and the reaction cost is reduced; the product yield is high, the halogen simple substance is co-produced, the additional value is high, a large amount of waste is prevented from being generated, and the method has high atom economy and environment friendliness and is beneficial to application and popularization.

A practical synthesis of ureas from 2-aminopicolines using microwave irradiation

Charris,Dominguez,Lopez

, p. 233 - 236 (2007/10/03)

Several symemetrically disubstituted ureas are synthesized by heating of urea with 2-aminopicoline analogues under enviromentally benign conditions without any solvent in a conventional microwave oven.

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