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10443-65-9

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10443-65-9 Usage

Uses

2-Bromoacrylic acid is used as a raw material on QSAR models to predict mutagenicity of acrylates. It is used as a pharmaceutical intermediate.

Check Digit Verification of cas no

The CAS Registry Mumber 10443-65-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,4,4 and 3 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 10443-65:
(7*1)+(6*0)+(5*4)+(4*4)+(3*3)+(2*6)+(1*5)=69
69 % 10 = 9
So 10443-65-9 is a valid CAS Registry Number.
InChI:InChI=1/C3H3BrO2/c1-2(4)3(5)6/h1H2,(H,5,6)/p-1

10443-65-9 Well-known Company Product Price

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

  • (L01194)  2-Bromoacrylic acid, 95%   

  • 10443-65-9

  • 1g

  • 146.0CNY

  • Detail
  • Alfa Aesar

  • (L01194)  2-Bromoacrylic acid, 95%   

  • 10443-65-9

  • 5g

  • 456.0CNY

  • Detail
  • Aldrich

  • (377376)  2-Bromoacrylicacid  95%

  • 10443-65-9

  • 377376-1G

  • 370.89CNY

  • Detail
  • Aldrich

  • (377376)  2-Bromoacrylicacid  95%

  • 10443-65-9

  • 377376-5G

  • 1,067.04CNY

  • Detail

10443-65-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-BROMOACRYLIC ACID

1.2 Other means of identification

Product number -
Other names 2-Bromopropenoic 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:10443-65-9 SDS

10443-65-9Relevant articles and documents

Synthesis of (α-T)polyacrylic acid

Postolache, Cristian,Matei, Lidia

, p. 444 - 445 (2007)

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Synthetic studies for novel structure of α-nitrogenously functionalized α-fluorocarboxylic acids. Part III. Some reactions of α-bromo-α-fluorocarboxylic acids and their ethyl esters with sodium azide

Takeuchi, Yoshio,Takagi, Kumiko,Yamaba, Tomokazu,Nabetani, Manabu,Koizumi, Toru

, p. 149 - 154 (1994)

Synthesis of a novel group of α-azido-α-fluorocarboxylic acid derivatives has been attempted by azidation of the corresponding α-bromo-α-fluorocarboxylic acids or ethyl esters.Although ethyl azidofluoroacetate was obtained, over-azidation occurred very readily in most cases to afford geminally diazidated compounds.Attemped conversion of ethyl azidofluoroacetate into azidofluoroacetic acid by alkaline hydrolysis or by treatment with trimethylsilyl bromide resulted mainly in the formation of defluorinated products.It was found that, although α-fluorocarboxylates are generally considered stable, defluorination occurs under nucleophilic conditions if an additional labilizing group is present on the same carbon atom as the fluorine.

Synthesis, thermal, mass and ab initio analyses of cyclopropane-1,1,2- tricarboxylic acid

Taoana,Holme,Bariyanga

, p. 173 - 178 (2004)

The preparation of cyclopropane-1,1,2-tricarboxylic acid from cyanoacetic acid and 2,3-dibropropionic acid has been done in one-step procedure in alkaline medium. The compound has been characterized, by nuclear magnetic resonance, mass spectrometry, and t

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