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3-CHLORO-4-FLUOROPHENYLMAGNESIUM BROMID&, an organometallic compound, is characterized by a magnesium atom bonded to a phenyl group, which features a fluorine and chlorine substituent. 3-CHLORO-4-FLUOROPHENYLMAGNESIUM BROMID& is renowned for its role as a reagent in organic synthesis, particularly in Grignard reactions, where it functions as a nucleophile to facilitate the formation of carbon-carbon bonds. Its versatility and widespread application in the synthesis of a range of organic compounds, including pharmaceuticals, agrochemicals, and materials, make it a valuable asset in the field of chemistry. It is typically synthesized in situ from the reaction of 3-chloro-4-fluorobenzene with magnesium and bromine.

413589-34-1

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413589-34-1 Usage

Uses

Used in Organic Synthesis:
3-CHLORO-4-FLUOROPHENYLMAGNESIUM BROMID& is used as a reagent for facilitating Grignard reactions, which are crucial for the formation of carbon-carbon bonds in organic compounds. Its nucleophilic properties make it an indispensable tool in the synthesis of a variety of organic molecules.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, 3-CHLORO-4-FLUOROPHENYLMAGNESIUM BROMID& is utilized as a key intermediate in the synthesis of complex organic molecules that have medicinal properties. Its ability to form carbon-carbon bonds is essential in creating the structural backbone of various pharmaceuticals.
Used in Agrochemical Industry:
3-CHLORO-4-FLUOROPHENYLMAGNESIUM BROMID& is employed as a reagent in the development of agrochemicals, such as pesticides and herbicides. Its role in forming carbon-carbon bonds is vital for constructing the molecular structures that exhibit the desired biological activity against pests and weeds.
Used in Materials Science:
In the field of materials science, 3-CHLORO-4-FLUOROPHENYLMAGNESIUM BROMID& is used as a precursor in the synthesis of advanced materials with specific properties. Its involvement in creating carbon-carbon bonds is crucial for the development of materials with tailored characteristics for various applications, such as electronics, coatings, and composites.

Check Digit Verification of cas no

The CAS Registry Mumber 413589-34-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,1,3,5,8 and 9 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 413589-34:
(8*4)+(7*1)+(6*3)+(5*5)+(4*8)+(3*9)+(2*3)+(1*4)=151
151 % 10 = 1
So 413589-34-1 is a valid CAS Registry Number.
InChI:InChI=1/C6H3ClF.BrH.Mg/c7-5-3-1-2-4-6(5)8;;/h2-4H;1H;/q;;+1/p-1/rC6H3BrClFMg/c7-10-4-1-2-6(9)5(8)3-4/h1-3H

413589-34-1 Well-known Company Product Price

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  • Aldrich

  • (563676)  3-Chloro-4-fluorophenylmagnesiumbromidesolution  0.5 M in THF

  • 413589-34-1

  • 563676-50ML

  • 3,038.49CNY

  • Detail

413589-34-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name magnesium,1-chloro-2-fluorobenzene-5-ide,bromide

1.2 Other means of identification

Product number -
Other names PC2947

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:413589-34-1 SDS

413589-34-1Relevant academic research and scientific papers

PYRROLIDINE DERIVATIVE

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Paragraph 0408, (2019/04/16)

The present invention aims to provide a novel compound which has CGRP receptor antagonist activity and which is useful for the treatment of various diseases mediated by CGRP receptors. That is, the present invention relates to the pyrrolidine derivatives represented by the following formula (I) or a pharmaceutically acceptable salt thereof. In the formulae, W is ring, X is a carbon atom or the like, Y1 to Y4 are carbon atoms or the like, and R1 to R7 is alkyl or the like. The compounds of the present invention or a pharmaceutically acceptable salt thereof have an excellent CGRP receptor antagonist activity, and thus are useful as agents for the treatment of various diseases mediated by CGRP receptors.

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