Welcome to LookChem.com Sign In|Join Free

CAS

  • or
3-Bromo-2-fluorobenzoic acid is an organic compound characterized by its off-white powder form. It features a benzoic acid structure with a bromine atom at the 3rd position and a fluorine atom at the 2nd position, which contributes to its unique chemical properties and potential applications in various industries.

161957-56-8 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 161957-56-8 Structure
  • Basic information

    1. Product Name: 3-Bromo-2-fluorobenzoic acid
    2. Synonyms: 3-Bromo-2-fluorobenzoic acid 97%;Benzoic acid, 3-bromo-2-fluoro-;BUTTPARK 14\01-30;3-BROMO-2-FLUOROBENZOIC ACID;3-Bromo-2-fluorobenzoic;3-Bromo-2-fluorobenzoic acid 97%+
    3. CAS NO:161957-56-8
    4. Molecular Formula: C7H4BrFO2
    5. Molecular Weight: 219.01
    6. EINECS: N/A
    7. Product Categories: Aromatic Carboxylic Acids, Amides, Anilides, Anhydrides & Salts;Benzoic acid;API intermediates;Acids and Derivatives;Halides
    8. Mol File: 161957-56-8.mol
  • Chemical Properties

    1. Melting Point: 168 °C
    2. Boiling Point: 298.2 °C at 760 mmHg
    3. Flash Point: 134.1 °C
    4. Appearance: white to off-white solid
    5. Density: 1.789 g/cm3
    6. Vapor Pressure: 9.41mmHg at 25°C
    7. Refractive Index: 1.438
    8. Storage Temp.: Sealed in dry,Room Temperature
    9. Solubility: N/A
    10. PKA: 2.88±0.10(Predicted)
    11. CAS DataBase Reference: 3-Bromo-2-fluorobenzoic acid(CAS DataBase Reference)
    12. NIST Chemistry Reference: 3-Bromo-2-fluorobenzoic acid(161957-56-8)
    13. EPA Substance Registry System: 3-Bromo-2-fluorobenzoic acid(161957-56-8)
  • Safety Data

    1. Hazard Codes: Xi
    2. Statements: 36
    3. Safety Statements: 26
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: IRRITANT
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 161957-56-8(Hazardous Substances Data)

161957-56-8 Usage

Uses

Used in Pharmaceutical Industry:
3-Bromo-2-fluorobenzoic acid is used as a reagent for the synthesis of Dabrafenib, a BRAF kinase inhibitor. 3-Bromo-2-fluorobenzoic acid is utilized in the treatment of BRAF V600-mutation positive carcinoma, as it targets the BRAF gene that plays a crucial role in cell growth and is often mutated in cancer cases.
Used in Allergy Treatment:
3-Bromo-2-fluorobenzoic acid is also used as a reagent to prepare Alkynlphenoxyacetic acid receptor agonists. These compounds have the potential to be used in the treatment of allergic inflammatory diseases, such as allergic rhinitis, by modulating the immune response and reducing inflammation.

Check Digit Verification of cas no

The CAS Registry Mumber 161957-56-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,1,9,5 and 7 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 161957-56:
(8*1)+(7*6)+(6*1)+(5*9)+(4*5)+(3*7)+(2*5)+(1*6)=158
158 % 10 = 8
So 161957-56-8 is a valid CAS Registry Number.
InChI:InChI=1/C4H2Br2F4/c1-2(5)3(7,8)4(6,9)10/h1H2

161957-56-8 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Alfa Aesar

  • (H50235)  3-Bromo-2-fluorobenzoic acid, 97%   

  • 161957-56-8

  • 1g

  • 697.0CNY

  • Detail
  • Alfa Aesar

  • (H50235)  3-Bromo-2-fluorobenzoic acid, 97%   

  • 161957-56-8

  • 5g

  • 3140.0CNY

  • Detail

161957-56-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Bromo-2-fluorobenzoic acid

1.2 Other means of identification

Product number -
Other names 3-Bromo-2-fluoro-benzoic acid

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:161957-56-8 SDS

161957-56-8Relevant articles and documents

TYK2 INHIBITORS AND USES THEREOF

-

Paragraph 00474, (2020/06/19)

The present invention provides compounds, compositions thereof, and methods of using the same for the inhibition of TYK2, and the treatment of TYK2-mediated disorders.

TRICYCLIC ASK1 INHIBITORS

-

Paragraph 0399; 0401, (2019/10/29)

Provided herein are compounds, preferably ASK1 inhibitor compounds, compositions thereof, and methods of their preparation, and methods of inhibiting ASK1 and methods for treating disorders mediated by ASK1.

TRPV4 ANTAGONISTS

-

Page/Page column 39-40, (2011/10/13)

The present invention relates to quinoline analogs, pharmaceutical compositions containing them and their use as TRPV4 antagonists.

INHIBITORS OF STEAROYL-COA DESATURASE

-

, (2009/06/27)

Provided herein are compounds of the formula (I): as well as pharmaceutically acceptable salts thereof, wherein the substituents are as those disclosed in the specification. These compounds, and the pharmaceutical compositions containing them, are useful for the treatment of diseases such as, for example, obesity.

Dual Pharmacophores - PDE4-Muscarinic Antagonistics

-

Page/Page column 47, (2009/08/18)

The present invention is directed to novel compounds of Formula (I) and pharmaceutically acceptable salts thereof, pharmaceutical compositions and their use as dual chromaphores having inhibitory activity against PDE4 and muscarinic acetylcholine receptors (mAChRs), and thus being useful for treating respiratory diseases.

Dual Pharmacophores - PDE4-Muscarinic Antagonistics

-

Page/Page column 50, (2009/08/18)

The present invention relates to novel compounds of Formula (I) and their use in the treatment of respiratory diseases, including anti-inflammatory and allergic diseases such as chronic obstructive pulmonary disease (COPD), asthma, rhinitis (e.g. allergic rhinitis), atopic dermatitis or psoriasis.

Dual Pharmacophores - PDE4-Muscarinic Antagonistics

-

Page/Page column 49, (2009/08/16)

The present invention is directed to novel compounds of Formula (I), pharmaceutical compositions and their use in therapy, for example as inhibitors of phosphodiesterase type IV (PDE4) and as antagonists of muscarinic acetylcholine receptors (mAChRs), in the treatment of/and or prophylaxis of respiratory diseases, including antiinflammatory and/or allergic diseases such as chronic obstructive pulmonary disease (COPD), asthma, rhinitis (e.g. allergic rhinitis), atopic dermatitis or psoriasis.

DUAL PHARMACOPHORES - PDE4-MUSCARINIC ANTAGONISTICS

-

Page/Page column 125, (2009/10/09)

The present invention is directed to novel compounds of Formula's (I) - (VI), and pharmaceutically acceptable salts thereof, pharmaceutical compositions and their use in therapy, for example as inhibitors of phosphodiesterase type IV (PDE4) and as antagonists of muscarinic acetylcholine receptors (mAChRs), in the treatment of and/or prophylaxis of respiratory diseases, including inflammatory and/or allergic diseases such as chronic obstructive pulmonary disease (COPD), asthma, rhinitis (e.g. allergic rhinitis), atopic dermatitis or psoriasis.

Design, synthesis, and pharmacological evaluation of N-bicyclo-5-chloro-1H-indole-2-carboxamide derivatives as potent glycogen phosphorylase inhibitors

Onda, Kenichi,Shiraki, Ryota,Ogiyama, Takashi,Yokoyama, Kazuhiro,Momose, Kazuhiro,Katayama, Naoko,Orita, Masaya,Yamaguchi, Tomohiko,Furutani, Masako,Hamada, Noritaka,Takeuchi, Makoto,Okada, Minoru,Ohta, Mitsuaki,Tsukamoto, Shin-ichi

experimental part, p. 10001 - 10012 (2009/04/06)

As a result of the various N-bicyclo-5-chloro-1H-indole-2-carboxamide derivatives with a hydroxy moiety synthesized in an effort to discover novel glycogen phosphorylase (GP) inhibitors, 5-chloro-N-(5-hydroxy-5,6,7,8-tetrahydronaphthalen-2-yl)-1H-indole-2

Tricyclic pharmacophore-based molecules as novel integrin αvβ3 antagonists. Part IV: Preliminary control of αvβ3 selectivity by meta-oriented substitution

Kubota, Dai,Ishikawa, Minoru,Ishikawa, Midori,Yahata, Naokazu,Murakami, Shoichi,Fujishima, Kazuyuki,Kitakaze, Masafumi,Ajito, Keiichi

, p. 4158 - 4181 (2007/10/03)

To establish the in vivo efficacy of αvβ3/αIIbβ3 dual antagonists possessing a tricyclic pharmacophore, a corresponding αvβ3-selective antagonist was required as a control. We initially too

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 161957-56-8