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52729-03-0

52729-03-0

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52729-03-0 Usage

Chemical Properties

yellow crystalline powder

Check Digit Verification of cas no

The CAS Registry Mumber 52729-03-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,7,2 and 9 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 52729-03:
(7*5)+(6*2)+(5*7)+(4*2)+(3*9)+(2*0)+(1*3)=120
120 % 10 = 0
So 52729-03-0 is a valid CAS Registry Number.
InChI:InChI=1/C7H2Cl2N2O6/c8-4-2(7(12)13)1-3(10(14)15)5(9)6(4)11(16)17/h1H,(H,12,13)/p-1

52729-03-0SDS

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 2,4-Dichloro-3,5-dinitrobenzoic Acid

1.2 Other means of identification

Product number -
Other names 2,4-DICHLORO-3,5-DINITROBENZOIC 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:52729-03-0 SDS

52729-03-0Relevant articles and documents

Kinetics of the nucleophilic substitution reactions of methyl 2,4-dichloro-3,5-dinitrobenzoate with piperidine, piperazine, morpholine and thiomorpholine in methanol and benzene

Fathalla, Magda F.,Hamed, Ezzat A.

, p. 413 - 416 (2007/10/03)

The kinetic of the nucleophilic substitution of methyl 2,4-dichloro-3,5- dinitrobenzoate with piperidine, piperazine, morpholine and thiomorpholine in methanol and benzene were determined spectrophotometrically at different amine concentrations and at temperatures ranging from 25 to 45 °C. The second order rate constants and the thermodynamic parameters show that the reactions are not amine catalysed and are greatly dependent of the nature of solvent and amine. UV, IR, 1H NMR, and elemental analysis are used to prove the aminodechlorination at C-2.

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