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2-Bromo-4-fluoro-6-(trifluoromethyl)aniline is a chemical compound that is frequently utilized in the domain of organic synthesis. It is an aromatic amine, characterized by the presence of a bromine, a fluorine, and a trifluoromethyl group attached to the aniline ring, which is a benzene ring with an amine (-NH2) group. The molecular formula of 2-BROMO-4-FLUORO-6-(TRIFLUOROMETHYL)ANILINE is C7H4BrF4N, signifying that it is composed of seven carbon atoms, four hydrogen atoms, one bromine atom, four fluorine atoms, and one nitrogen atom. Due to its potential to cause irritation to the eyes, skin, and respiratory system, it is essential to handle this substance with caution. It is typically found in a solid state and is soluble in organic solvents. This chemical is generally stored in a cool, dry place to maintain its stability. It is predominantly used in research settings rather than in commercial or domestic applications.

875664-27-0

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875664-27-0 Usage

Uses

Used in Organic Synthesis:
2-Bromo-4-fluoro-6-(trifluoromethyl)aniline is used as a key intermediate in the synthesis of various organic compounds for [application reason]. Its unique structure, featuring a bromine, a fluorine, and a trifluoromethyl group, makes it a valuable building block in the creation of complex molecules.
Used in Research Environments:
In the field of scientific research, 2-Bromo-4-fluoro-6-(trifluoromethyl)aniline is used as a reagent or a precursor for [application reason]. Its properties and reactivity are studied to understand its potential applications in the development of new materials and compounds.
Used in Pharmaceutical Industry:
2-Bromo-4-fluoro-6-(trifluoromethyl)aniline is used as a starting material for the synthesis of pharmaceutical compounds for [application reason]. Its presence in the molecular structure can influence the activity and selectivity of the resulting drug molecules, making it an important component in drug discovery and development processes.
Used in Chemical Industry:
In the chemical industry, 2-Bromo-4-fluoro-6-(trifluoromethyl)aniline is used as a specialty chemical for [application reason]. Its unique combination of functional groups can be exploited to produce a range of products with specific properties and applications in various sectors.

Check Digit Verification of cas no

The CAS Registry Mumber 875664-27-0 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, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 875664-27:
(8*8)+(7*7)+(6*5)+(5*6)+(4*6)+(3*4)+(2*2)+(1*7)=220
220 % 10 = 0
So 875664-27-0 is a valid CAS Registry Number.
InChI:InChI=1/C7H4BrF4N/c8-5-2-3(9)1-4(6(5)13)7(10,11)12/h1-2H,13H2

875664-27-0 Well-known Company Product Price

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  • Alfa Aesar

  • (H26206)  2-Bromo-4-fluoro-6-(trifluoromethyl)aniline, 98%   

  • 875664-27-0

  • 1g

  • 336.0CNY

  • Detail
  • Alfa Aesar

  • (H26206)  2-Bromo-4-fluoro-6-(trifluoromethyl)aniline, 98%   

  • 875664-27-0

  • 10g

  • 1940.0CNY

  • Detail

875664-27-0SDS

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 2-Bromo-4-fluoro-6-(trifluoromethyl)aniline

1.2 Other means of identification

Product number -
Other names 2-BROMO-4-FLUORO-6-(TRIFLUOROMETHYL)ANILINE

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:875664-27-0 SDS

875664-27-0Relevant articles and documents

QUINOXALINE DERIVATIVES

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Page/Page column 44, (2021/07/24)

The present invention relates to compounds according to general formula (I), which act as modulators of the glucocorticoid receptor and can be used in the treatment and/or prophylaxis of disorders which are at least partially mediated by the glucocorticoid receptor.

SUBSTITUTED TRIAZOLO QUINOXALINE DERIVATIVES

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Page/Page column 63, (2020/02/14)

The present invention relates to compounds according to general formula (I) which act as modulators of the glucocorticoid receptor and can be used in the treatment and/or prophylaxis of disorders which are at least partially mediated by the glucocorticoid receptor.

COMPOUNDS AND COMPOSITIONS FOR TREATING CONDITIONS ASSOCIATED WITH NLRP ACTIVITY

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Page/Page column 457, (2019/02/13)

In one aspect, compounds of Formula AA, or a pharmaceutically acceptable salt thereof, are featured. The variables shown in Formula AA are as defined in the claims. The compounds of formula AA are NLRP3 activity modulators and, as such, can be used in the treatment of metabolic disorders (e.g. Type 2 diabetes, atherosclerosis, obesity or gout), a disease of the central nervous system (e.g. Alzheimer's disease, multiple sclerosis, Amyotrophic Lateral Sclerosis or Parkinson's disease), lung disease (e.g. asthma, COPD or pulmonary idiopathic fibrosis), liver disease (e.g. NASH syndrome, viral hepatitis or cirrhosis), pancreatic disease (e.g. acute pancreatitis or chronic pancreatitis), kidney disease (e.g. acute kidney injury or chronic kidney injury), intestinal disease (e.g. Crohn's disease or Ulcerative Colitis), skin disease (e.g. psoriasis), musculoskeletal disease (e.g. scleroderma), a vessel disorder (e.g. giant cell arteritis), a disorder of the bones (e.g. osteoarthritis, osteoporosis or osteopetrosis disorders), eye disease (e.g. glaucoma or macular degeneration), a disease caused by viral infection (e.g. HIV or AIDS), an autoimmune disease (e.g. Rheumatoid Arthritis, Systemic Lupus Erythematosus or Autoimmune Thyroiditis), cancer or aging.

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