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1261629-31-5

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1261629-31-5 Usage

General Description

2-Chloro-4-(difluoromethyl)pyrimidine is a chemical compound with the molecular formula C5H2ClF2N2. It is a pyrimidine derivative with a chlorine atom at the 2-position and a difluoromethyl group at the 4-position. 2-CHLORO-4-(DIFLUOROMETHYL)PYRIMIDINE is commonly used as an intermediate in the synthesis of pharmaceuticals and agricultural chemicals. It is also used in the production of herbicides, fungicides, and insecticides. 2-Chloro-4-(difluoromethyl)pyrimidine is a highly reactive and versatile building block in organic synthesis, making it a valuable compound in the chemical industry. Additionally, it is important to handle this compound with caution, as it is toxic and may pose health risks if not handled properly.

Check Digit Verification of cas no

The CAS Registry Mumber 1261629-31-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,1,6,2 and 9 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1261629-31:
(9*1)+(8*2)+(7*6)+(6*1)+(5*6)+(4*2)+(3*9)+(2*3)+(1*1)=145
145 % 10 = 5
So 1261629-31-5 is a valid CAS Registry Number.

1261629-31-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-chloro-4-(difluoromethyl)pyrimidine

1.2 Other means of identification

Product number -
Other names 2-chloro-4-difluoromethyl-pyrimidine

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:1261629-31-5 SDS

1261629-31-5Downstream Products

1261629-31-5Relevant articles and documents

The direct C-H difluoromethylation of heteroarenes based on the photolysis of hypervalent iodine(III) reagents that contain difluoroacetoxy ligands

Sakamoto, Ryu,Kashiwagi, Hirotaka,Maruoka, Keiji

, p. 5126 - 5129 (2017)

In this letter, an efficient method for the photolytic generation of difluoromethyl radicals from [bis(difluoroacetoxy)iodo]benzene reagents is described. The present approach enables the introduction of difluoromethyl groups into various heteroarenes und

THIAZOLE-SUBSTITUTED AMINOHETEROARYLS AS SPLEEN TYROSINE KINASE INHIBITORS

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Paragraph 00189, (2015/07/07)

The invention provides certain thiazole-substituted aminoheteroaryl compounds of the Formula (I) or pharmaceutically acceptable salts thereof, wherein ring R1, R2, R3, R4, ring B, and the subscript r are as defi

THIAZOLE-SUBSTITUTED AMINOHETEROARYLS AS SPLEEN TYROSINE KINASE INHIBITORS

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Paragraph 00203, (2014/11/13)

The invention provides certain thiazole-substituted aminoheteroaryl compounds of the Formula (I) or pharmaceutically acceptable salts thereof, wherein X1, X2, X3, X4, Y1, Y2, Y3, Y4, and R4 are as defined herein. The invention also provides pharmaceutical compositions comprising such compounds, and methods of using the compounds for treating diseases or conditions mediated by Spleen Tyrosine Kinase (Syk).

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