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4-BROMO-1-(DIFLUOROMETHYL)-1H-PYRAZOLE is a pyrazole derivative with the chemical formula C4H3BrF2N2. It features a bromine atom and a difluoromethyl group attached to the pyrazole ring, which endows it with versatile reactivity and potential applications in various fields.
Used in Pharmaceutical Industry:
4-BROMO-1-(DIFLUOROMETHYL)-1H-PYRAZOLE is used as a building block for the synthesis of biologically active molecules, contributing to the development of new drugs and therapeutic agents.
Used in Agrochemical Industry:
4-BROMO-1-(DIFLUOROMETHYL)-1H-PYRAZOLE is used as a component in the creation of agrochemicals, potentially enhancing crop protection and yield.
Used in Organic Synthesis:
4-BROMO-1-(DIFLUOROMETHYL)-1H-PYRAZOLE is used as a reagent in organic synthesis, facilitating the production of a variety of chemical compounds.
Used in Chemical Research:
4-BROMO-1-(DIFLUOROMETHYL)-1H-PYRAZOLE is used as a research tool in the study of pyrazole chemistry and related fields, aiding in the exploration of new chemical reactions and mechanisms.

956477-67-1

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956477-67-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 956477-67-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,6,4,7 and 7 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 956477-67:
(8*9)+(7*5)+(6*6)+(5*4)+(4*7)+(3*7)+(2*6)+(1*7)=231
231 % 10 = 1
So 956477-67-1 is a valid CAS Registry Number.

956477-67-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-bromo-1-(difluoromethyl)pyrazole

1.2 Other means of identification

Product number -
Other names 4-Bromo-1-(difluoromethyl)-1H-pyrazole

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:956477-67-1 SDS

956477-67-1Relevant academic research and scientific papers

Pyridazinol compound and derivatives, preparation method, weeding compositions and application thereof

-

Paragraph 0214-0216, (2021/02/24)

The invention belongs to the technical field of pesticides, and particularly relates to a pyridazinol compound and derivatives, a preparation method, weeding compositions and application thereof. Thepyridazinol compound is shown as a general formula I whi

N-Difluoromethylation of imidazoles and pyrazoles using BrCF2PO(OEt)2 under mild condition

Mao, Ting,Zhao, Liang,Huang, Yang,Lou, Yue-Guang,Yao, Qiuli,Li, Xiao-Fei,He, Chun-Yang

supporting information, p. 2752 - 2754 (2018/06/12)

A simple and efficient protocol for the direct N-difluoromethylation of imidazoles and pyrazoles has been developed. The reaction makes use of commercially available, non-ozone-depleting and easy handling BrCF2PO(OEt)2 as difluorocarbene precursor, and provides a cost-efficient and environmentally benign access to some difluoromethylated biologically relevant molecules.

Chemical properties of derivatives of N-difluoromethyl-and N-2-H-tetrafluoroethylpyrazoles

Petko,Sokolenko,Yagupolskii

, p. 1177 - 1184 (2008/09/20)

Nitration, chlorination, bromination, and iodination reactions have been investigated for pyrazole derivatives containing a difluoromethylene fragment directly on a nitrogen atom. Conditions have been found for introducing a cyano group into the nucleus of N-2-H-tetrafluoroethylpyrazole and converting it into carboxyl or tetrazole functions. Springer Science+Business Media, Inc. 2006.

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