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643-43-6

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643-43-6 Usage

Chemical Properties

beige crystalline powder

Uses

2,4-Dinitrophenylacetic acid was used in the preparation of 2-hydroxy-4-nitrohenzonitrile, required for the synthesis of parabactin azide (catecholamide siderophore photoaffinity label).

General Description

Coupling of 2,4-dinitrophenylacetic acid with diazonium salts has been reported.

Purification Methods

Crystallise the acid from H2O. [Beilstein 9 IV 1691.]

Check Digit Verification of cas no

The CAS Registry Mumber 643-43-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,4 and 3 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 643-43:
(5*6)+(4*4)+(3*3)+(2*4)+(1*3)=66
66 % 10 = 6
So 643-43-6 is a valid CAS Registry Number.
InChI:InChI=1/C8H6N2O6/c11-8(12)3-5-1-2-6(9(13)14)4-7(5)10(15)16/h1-2,4H,3H2,(H,11,12)/p-1

643-43-6 Well-known Company Product Price

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  • Alfa Aesar

  • (B22102)  2,4-Dinitrophenylacetic acid, 98%   

  • 643-43-6

  • 25g

  • 577.0CNY

  • Detail
  • Alfa Aesar

  • (B22102)  2,4-Dinitrophenylacetic acid, 98%   

  • 643-43-6

  • 100g

  • 1847.0CNY

  • Detail

643-43-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4-DINITROPHENYLACETIC ACID

1.2 Other means of identification

Product number -
Other names 2-(2,4-dinitrophenyl)acetic 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:643-43-6 SDS

643-43-6Relevant articles and documents

-

Martinuzzi,Vecchi

, p. 671 (1952)

-

Orientation Effect of Side Chain Substituents in Aromatic Substitution. Induced Ortho Nitration

Strazzolini, Paolo,Verardo, Giancarlo,Gorassini, Fausto,Giumanini, Angelo G.

, p. 1155 - 1161 (2007/10/02)

The presence of a free carboxyl or ester function on the α-carbon of toluene induces the nitration of the phenyl ring in the ortho position at or above the statistical value (chaperon effect), when pure HNO3 is used in CH2Cl2 solution.This is at variance with the results of classical nitration in H2SO4, where p-nitration predominates by far and m-nitration occurs at a remarkable extent.The new finding is explained in terms of precomplex formation.

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