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363-47-3

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363-47-3 Usage

Description

Benzenamine, 3,5-difluoro-4-methoxy(9CI), also known as 3,5-Difluoro-4-methoxyaniline, is an organic compound belonging to the class of aniline derivatives. It is characterized by the presence of a fluorine atom at the 3rd and 5th positions, and a methoxy group at the 4th position of the benzene ring. This light brown solid exhibits unique chemical properties that make it suitable for various applications.

Uses

Used in Chemical Synthesis:
Benzenamine, 3,5-difluoro-4-methoxy(9CI) is used as a key intermediate in the synthesis of various organic compounds, particularly those with pharmaceutical or agrochemical applications. Its unique substitution pattern allows for selective functionalization and the formation of a wide range of derivatives.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, Benzenamine, 3,5-difluoro-4-methoxy(9CI) is used as a building block for the development of novel drugs. Its unique structure and reactivity enable the creation of new molecules with potential therapeutic properties, targeting a variety of diseases and conditions.
Used in Dye and Pigment Industry:
Benzenamine, 3,5-difluoro-4-methoxy(9CI) is also utilized in the dye and pigment industry for the production of high-performance dyes and pigments. Its distinctive chemical structure contributes to the development of dyes with improved color strength, stability, and fastness properties.
Used in conjunction with Thermal Energy:
Benzenamine, 3,5-difluoro-4-methoxy(9CI) is employed in applications that involve the use of thermal energy, such as in the manufacturing of heat-sensitive materials or in thermal energy storage systems. Its unique properties allow for efficient energy transfer and improved performance in these applications.

Check Digit Verification of cas no

The CAS Registry Mumber 363-47-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,6 and 3 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 363-47:
(5*3)+(4*6)+(3*3)+(2*4)+(1*7)=63
63 % 10 = 3
So 363-47-3 is a valid CAS Registry Number.
InChI:InChI=1/C7H7F2NO/c1-11-7-5(8)2-4(10)3-6(7)9/h2-3H,10H2,1H3

363-47-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,5-Difluoro-4-methoxyaniline

1.2 Other means of identification

Product number -
Other names 3,5-difluoro-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:363-47-3 SDS

363-47-3Relevant articles and documents

AMINATION AND HYDROXYLATION OF ARYLMETAL COMPOUNDS

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Paragraph 0098; 0134; 0135; 0186, (2018/03/25)

In one aspect, the present disclosure provides methods of preparing a primary or secondary amine and hydroxylated aromatic compounds. In some embodiments, the aromatic compound may be unsubstituted, substituted, or contain one or more heteroatoms within the rings of the aromatic compound. The methods described herein may be carried out without the need for transition metal catalysts or harsh reaction conditions.

NOVEL FLUORESCENT DYES AND USES THEREOF

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Page/Page column 32-33, (2011/02/24)

The present invention provides fluorescent dyes that are based on firefly luciferin structure. These dyes are optimally excited at shorter wavelengths and have Stokes shift of at least 50 nm. The fluorescent dyes of the invention are useful for preparation of dye-conjugates, which can be used in detection of an analyte in a sample.

Electrophilic aromatic fluorination with fluorine: meta-Directed fluorination of anilines

Alric,Marquet,Billard,Langlois

, p. 661 - 667 (2007/10/03)

Anilines are mainly or selectively fluorinated in the meta-position with F2 when dissolved in triflic acid, sometimes in the presence of small quantities of antimony pentafluoride. The regioselectivity is increased when an electron-donating substituent is present at the para-position.

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