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21739-93-5

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21739-93-5 Usage

Chemical Properties

white to light yellow crystal powder

Check Digit Verification of cas no

The CAS Registry Mumber 21739-93-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,7,3 and 9 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 21739-93:
(7*2)+(6*1)+(5*7)+(4*3)+(3*9)+(2*9)+(1*3)=115
115 % 10 = 5
So 21739-93-5 is a valid CAS Registry Number.
InChI:InChI=1/C7H4BrClO2/c8-6-2-1-4(9)3-5(6)7(10)11/h1-3H,(H,10,11)/p-1

21739-93-5 Well-known Company Product Price

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

  • (A10103)  2-Bromo-5-chlorobenzoic acid, 98+%   

  • 21739-93-5

  • 1g

  • 648.0CNY

  • Detail
  • Alfa Aesar

  • (A10103)  2-Bromo-5-chlorobenzoic acid, 98+%   

  • 21739-93-5

  • 5g

  • 1154.0CNY

  • Detail
  • Alfa Aesar

  • (A10103)  2-Bromo-5-chlorobenzoic acid, 98+%   

  • 21739-93-5

  • 25g

  • 4529.0CNY

  • Detail

21739-93-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Bromo-5-chlorobenzoic acid

1.2 Other means of identification

Product number -
Other names 2-bromo5-chloro-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:21739-93-5 SDS

21739-93-5Downstream Products

21739-93-5Relevant articles and documents

FLOW REACTION PROCESS FOR MANUFACTURE OF BORON-CONTAINING AGROCHEMICALS

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Paragraph 0107, (2021/02/05)

The present invention relates to methods of preparing benzoxaboroles. Benzoxaborole compounds have shown promise as antimicrobial agents, especially against fungal pathogens. The invention also relates to compositions of acyclic alkoxy boronic acid esters as intermediates, and continuous flow processes of mixing the intermediates with organomagnesium, magnesium, or organolithium reagents to form the desired benzoxaboroles.

Thrombin inhibitors

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, (2008/06/13)

Compounds of the invention are useful in inhibiting thrombin and associated thrombotic occlusions having the following structure: or a pharmaceutically acceptable salt thereof, e.g. where R3 is —CH2NH2, —CH2CH2NH2, or —CH2NHC(O)OC(CH3)3.

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