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700-36-7

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700-36-7 Usage

Chemical Properties

Yellow to pale green powder

Check Digit Verification of cas no

The CAS Registry Mumber 700-36-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,0 and 0 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 700-36:
(5*7)+(4*0)+(3*0)+(2*3)+(1*6)=47
47 % 10 = 7
So 700-36-7 is a valid CAS Registry Number.
InChI:InChI=1/C6H3BrFNO2/c7-5-3-4(8)1-2-6(5)9(10)11/h1-3H

700-36-7 Well-known Company Product Price

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  • (Code)Product description
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  • Alfa Aesar

  • (H61466)  2-Bromo-4-fluoro-1-nitrobenzene, 98%   

  • 700-36-7

  • 5g

  • 364.0CNY

  • Detail
  • Alfa Aesar

  • (H61466)  2-Bromo-4-fluoro-1-nitrobenzene, 98%   

  • 700-36-7

  • 25g

  • 1313.0CNY

  • Detail
  • Alfa Aesar

  • (H61466)  2-Bromo-4-fluoro-1-nitrobenzene, 98%   

  • 700-36-7

  • 100g

  • 4166.0CNY

  • Detail

700-36-7SDS

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-Bromo-4-fluoro-1-nitrobenzene

1.2 Other means of identification

Product number -
Other names 4-Fluor-2-brom-1-nitro-benzol

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:700-36-7 SDS

700-36-7Relevant articles and documents

Preparation method of 3-bromo-4-bromonitrophenol

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Paragraph 0009-0011; 0013-0015, (2019/03/08)

The invention discloses an industrial preparation method of 3-bromo-4-bromonitrophenol. According to the industrial preparation method of the 3-bromo-4-bromonitrophenol, p-fluoroaniline serves as an initial raw material, and the 3-bromo-4-bromonitrophenol

Decarboxylative Halogenation and Cyanation of Electron-Deficient Aryl Carboxylic Acids via Cu Mediator as Well as Electron-Rich Ones through Pd Catalyst under Aerobic Conditions

Fu, Zhengjiang,Li, Zhaojie,Song, Yuanyuan,Yang, Ruchun,Liu, Yanzhu,Cai, Hu

, p. 2794 - 2803 (2016/04/26)

Simple strategies for decarboxylative functionalizations of electron-deficient benzoic acids via using Cu(I) as promoter and electron-rich ones by employing Pd(II) as catalyst under aerobic conditions have been established, which lead to smooth synthesis of aryl halides (-I, Br, and Cl) through the decarboxylative functionalization of benzoic acids with readily available halogen sources CuX (X = I, Br, Cl), and easy preparation of benzonitriles from decarboxylative cyanation of aryl carboxylic acids with nontoxic and low-cost K4Fe(CN)6 under an oxygen atmosphere for the first time.

NITROGENOUS HETEROCYCLIC DERIVATIVES AND THEIR APPLICATION IN DRUGS

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Paragraph 00424, (2014/02/15)

The present invention relates to the field of medicine, provided herein are novel nitrogenous heterocyclic compounds, their preparation methods and their uses as drugs, especially for treatment and prevention of tissue fibrosis. Also provided herein are pharmaceutically acceptable compositions comprising the nitrogenous heterocyclic compounds and the uses of the compositions in the treatment of human or animal tissue fibrosis, especially for human or animal renal interstitial fibrosis, glomerular sclerosis, liver fibrosis, pulmonary fibrosis, peritoneal fibrosis, myocardial fibrosis, dermatofibrosis, postsurgical adhesion, benign prostatic hyperplasia, skeletal muscle fibrosis, scleroderma, multiple sclerosis, pancreatic fibrosis, cirrhosis, myosarcoma, neurofibroma, pulmonary interstitial fibrosis, diabetic nephropathy, alzheimer disease or vascular fibrosis.

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