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610-28-6

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610-28-6 Usage

General Description

2,5-Dinitrobenzoic acid is a benzoic acid derivative. Its proton, deuteron and proton spin-lattice relaxation times have been evaluated by using Schr?dinger wave equation.

Purification Methods

Crystallise the acid from distilled H2O. Dry it in a vacuum desiccator. [Beilstein 9 II 279, 9 III 1778, 9 IV 1241.]

Check Digit Verification of cas no

The CAS Registry Mumber 610-28-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,1 and 0 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 610-28:
(5*6)+(4*1)+(3*0)+(2*2)+(1*8)=46
46 % 10 = 6
So 610-28-6 is a valid CAS Registry Number.
InChI:InChI=1/C7H4N2O6/c10-7(11)5-3-4(8(12)13)1-2-6(5)9(14)15/h1-3H,(H,10,11)/p-1

610-28-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,5-DINITROBENZOIC ACID

1.2 Other means of identification

Product number -
Other names 2,5-Dinitro-benzoesaeure

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:610-28-6 SDS

610-28-6Relevant articles and documents

PROCESS FOR PREPARING SUBSTITUTED AROMATIC CARBOXYLIC ACIDS

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Page/Page column 3, (2010/09/17)

A process for preparing an aromatic carboxylic acid having a heteroatom containing substituent is provided that includes reaction in a vessel of an aromatic precursor having an aromatic core with at least one heteroatom containing substituent and at least one hydrogen extending from the core, with a haloacetonitrile under reaction conditions to form an aromatic acetonitrile with an acetonitrile moiety. The aromatic acetonitrile is exposed to an oxidizing agent under conditions to convert the acetonitrile moiety to a carboxylic acid group to prepare the aromatic carboxylic acid having the heteroatom containing substituent.

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