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3-Bromo-5-fluoro-4-methoxyaniline is a chemical compound characterized by the molecular formula C7H7BrFNO and a molecular weight of 221.04 g/mol. It is a substituted aniline derivative featuring a bromine atom at the 3 position, a fluorine atom at the 5 position, and a methoxy group at the 4 position. 3-BROMO-5-FLUORO-4-METHOXYANILINE is known for its versatile chemical structure and properties, making it a valuable building block in the synthesis of various complex chemical compounds.

875664-44-1

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875664-44-1 Usage

Uses

Used in Pharmaceutical Industry:
3-Bromo-5-fluoro-4-methoxyaniline is used as an intermediate in the synthesis of pharmaceuticals for its ability to contribute to the development of new drugs with specific therapeutic properties. Its unique structure allows for the creation of molecules with targeted actions, enhancing the effectiveness of medications.
Used in Agrochemical Industry:
In the agrochemical sector, 3-bromo-5-fluoro-4-methoxyaniline is utilized as a precursor in the production of agrochemicals, such as pesticides and herbicides. Its incorporation into these compounds can lead to improved performance and selectivity in agricultural applications.
Used in Dye Industry:
3-Bromo-5-fluoro-4-methoxyaniline is used as a key intermediate in the synthesis of dyes, where its distinct chemical structure contributes to the color and properties of the final dye products. This makes it valuable for applications requiring specific color characteristics and stability.
Used in Organic Synthesis and Research:
3-Bromo-5-fluoro-4-methoxyaniline serves as a building block in organic synthesis, allowing chemists to construct more complex molecules for research purposes. Its unique combination of functional groups facilitates the development of novel compounds with potential applications in various fields of chemistry and material science.

Check Digit Verification of cas no

The CAS Registry Mumber 875664-44-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,5,6,6 and 4 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 875664-44:
(8*8)+(7*7)+(6*5)+(5*6)+(4*6)+(3*4)+(2*4)+(1*4)=221
221 % 10 = 1
So 875664-44-1 is a valid CAS Registry Number.
InChI:InChI=1/C7H7BrFNO/c1-11-7-5(8)2-4(10)3-6(7)9/h2-3H,10H2,1H3

875664-44-1 Well-known Company Product Price

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  • Alfa Aesar

  • (H26152)  3-Bromo-5-fluoro-4-methoxyaniline, 98%   

  • 875664-44-1

  • 250mg

  • 851.0CNY

  • Detail
  • Alfa Aesar

  • (H26152)  3-Bromo-5-fluoro-4-methoxyaniline, 98%   

  • 875664-44-1

  • 1g

  • 2176.0CNY

  • Detail

875664-44-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Bromo-5-fluoro-4-methoxyaniline

1.2 Other means of identification

Product number -
Other names 3-BROMO-5-FLUORO-4-METHOXYANILINE

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:875664-44-1 SDS

875664-44-1Downstream Products

875664-44-1Relevant articles and documents

Preparation method of 2-bromo-6-fluoroanisole

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Paragraph 0025; 0031-0032; 0037; 0043-0044; 0047; 0053-0054, (2021/09/11)

The invention discloses a preparation method of 2-bromine-6-fluoroanisole, the preparation method comprises the following specific steps: (1) carrying out electrophilic substitution reaction on 3, 4-difluoronitrobenzene and bromosuccinimide to generate a compound III; (2) reacting the compound III with sodium methoxide to generate a compound IV; (3) reducing the compound IV by sodium hydrosulfite to generate a compound V; (4) performing diazotization deamination on the compound V to generate a compound I; the obtained product is 2-bromo-6-fluoroanisole. The preparation method is higher in yield.

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