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259269-84-6

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259269-84-6 Usage

General Description

2-AMINO-3-BROMO-5-FLUOROBENZOIC ACID is a chemical compound with the molecular formula C7H5BrFNO2. It is a derivative of benzoic acid and is composed of a benzene ring substituted with a bromine atom, a fluorine atom, and an amino group. 2-AMINO-3-BROMO-5-FLUOROBENZOIC ACID is commonly used as a building block in the synthesis of various pharmaceuticals and agrochemicals. It has also been studied for its potential use as an anti-influenza and anti-cancer agent. Additionally, 2-AMINO-3-BROMO-5-FLUOROBENZOIC ACID is a useful intermediate in the production of fluorescent dyes and textile dyes.

Check Digit Verification of cas no

The CAS Registry Mumber 259269-84-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,9,2,6 and 9 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 259269-84:
(8*2)+(7*5)+(6*9)+(5*2)+(4*6)+(3*9)+(2*8)+(1*4)=186
186 % 10 = 6
So 259269-84-6 is a valid CAS Registry Number.
InChI:InChI=1/C7H5BrFNO2/c8-5-2-3(9)1-4(6(5)10)7(11)12/h1-2H,10H2,(H,11,12)

259269-84-6 Well-known Company Product Price

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  • Alfa Aesar

  • (H66628)  2-Amino-3-bromo-5-fluorobenzoic acid, 95%   

  • 259269-84-6

  • 250mg

  • 1078.0CNY

  • Detail
  • Alfa Aesar

  • (H66628)  2-Amino-3-bromo-5-fluorobenzoic acid, 95%   

  • 259269-84-6

  • 1g

  • 3224.0CNY

  • Detail

259269-84-6SDS

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 2-AMINO-3-BROMO-5-FLUOROBENZOIC ACID

1.2 Other means of identification

Product number -
Other names 2-Amino-3-Bromo-5-Fluorobenzoic 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:259269-84-6 SDS

259269-84-6Upstream product

259269-84-6Relevant articles and documents

Amide derivative and preparation method and application thereof

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Paragraph 0058-0065, (2019/10/23)

The invention relates to an amide derivative and a preparation method and application thereof. The compound is an amide derivative containing 3-bromo-5-chloro (bromo) phenyl units, has obvious insecticidal activity, and can be used for killing various bio

FUSED RING PYRIMIDINE COMPOUND, INTERMEDIATE, AND PREPARATION METHOD, COMPOSITION AND USE THEREOF

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Paragraph 0502-0503, (2018/08/12)

Disclosed area fused ring pyrimidine compound, and an intermediate, a preparation method, a composition and a use thereof. The fused ring pyrimidine compound is a compound as shown in formula I, a tautomer, an enantiomer, a diastereoisomer, a pharmaceutically acceptable salt, a metabolite, a metabolic precursor or a prodrug thereof, wherein the above-mentioned compound is used for the preparation of a medicine for preventing, remitting or treating one or more of immune system diseases, autoimmune diseases, cell proliferative diseases, allergic disorders and cardiovascular diseases, and the compound has a strong inhibitory effect on the Janues kinase, FGFR kinase, FLT3 kinase and Src family kinase.

Preparation of 6-aminoquinazolin-4(3H)-ones via direct SNAr on the quinazoline ring

Barlaam, Bernard,Harris, Craig S.,Lecoq, Jonathan,Nguyen, Ha Thi Hoang

experimental part, p. 534 - 543 (2012/01/06)

The preparation of 6-aminoquinazolin-4(3H)-ones requires the use of platinum-metal group catalysis on the corresponding C-6-iodo or 6-bromo precursors. Herein, we report to our knowledge the first successful S NAr reaction directly at the unact

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