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717094-51-4

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717094-51-4 Usage

Description

Benzenemethanamine, 2,4-difluoro-3-methoxy(9CI) is a fluoro-substituted aniline derivative with the molecular formula C8H8F2NO. It features a benzene ring attached to a methanamine group, along with fluorine and methoxy substituents at specific positions. This chemical compound is widely utilized in organic synthesis and pharmaceutical research as a key building block for the development of various drugs and biologically active molecules.

Uses

Used in Pharmaceutical Research and Development:
Benzenemethanamine, 2,4-difluoro-3-methoxy(9CI) is employed as a key intermediate in the synthesis of various pharmaceuticals. Its unique structure and functional groups make it a valuable component in the creation of new drugs and therapeutic agents.
Used in Organic Synthesis:
In the field of organic synthesis, Benzenemethanamine, 2,4-difluoro-3-methoxy(9CI) serves as a versatile building block for the development of a wide range of chemical compounds. Its fluoro and methoxy substituents provide opportunities for further functionalization and modification, enabling the synthesis of diverse molecules with potential applications in various industries.
Used in Agrochemicals:
Benzenemethanamine, 2,4-difluoro-3-methoxy(9CI) may have potential applications in the agrochemical industry. Its unique structure and properties could be harnessed in the development of new pesticides, herbicides, or other agrochemical products, contributing to more effective and targeted agricultural solutions.
Used in Materials Science:
In the field of materials science, Benzenemethanamine, 2,4-difluoro-3-methoxy(9CI) could be utilized in the development of novel materials with specific properties. Its fluoro and methoxy substituents may impart unique characteristics to the resulting materials, making them suitable for various applications, such as coatings, adhesives, or advanced materials for electronics and other industries.
Overall, Benzenemethanamine, 2,4-difluoro-3-methoxy(9CI) is a versatile and valuable chemical compound with diverse potential uses across various industries, including pharmaceuticals, organic synthesis, agrochemicals, and materials science. Its unique structure and functional groups make it a key intermediate in the production of various chemicals and pharmaceuticals, contributing to the advancement of these fields.

Check Digit Verification of cas no

The CAS Registry Mumber 717094-51-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,1,7,0,9 and 4 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 717094-51:
(8*7)+(7*1)+(6*7)+(5*0)+(4*9)+(3*4)+(2*5)+(1*1)=164
164 % 10 = 4
So 717094-51-4 is a valid CAS Registry Number.

717094-51-4 Well-known Company Product Price

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  • (Code)Product description
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  • Alfa Aesar

  • (H26270)  2,4-Difluoro-3-methoxybenzylamine, 97%   

  • 717094-51-4

  • 1g

  • 1930.0CNY

  • Detail
  • Alfa Aesar

  • (H26270)  2,4-Difluoro-3-methoxybenzylamine, 97%   

  • 717094-51-4

  • 5g

  • 5958.0CNY

  • Detail

717094-51-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (2,4-difluoro-3-methoxyphenyl)methanamine

1.2 Other means of identification

Product number -
Other names JRD-1458

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:717094-51-4 SDS

717094-51-4Relevant articles and documents

2,6-difluorophenol as a bioisostere of a carboxylic acid: Bioisosteric analogues of γ-aminobutyric acid

Qiu, Jian,Stevenson, Scott H.,O'Beirne, Michael J.,Silverman, Richard B.

, p. 329 - 332 (2007/10/03)

3-(Aminomethyl)-2,6-difluorophenol (6) and 4-(aminomethyl)-2,6- difluorophenol (7) were synthesized in eight and four steps, respectively, starting from 2,6-difluorophenol, to test the potential of the 2,6- difluorophenol moiety to act as a lipophilic bio

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