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2602-36-0

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2602-36-0 Usage

General Description

2,6-DIMETHYL-3,5-PYRIDINEDICARBOXYLIC ACID, also known as dimethyl pyridine-3,5-dicarboxylate, is a chemical compound with the molecular formula C10H11NO4. It is a derivative of pyridine and a member of the pyridinedicarboxylic acid family. 2,6-DIMETHYL-3,5-PYRIDINEDICARBOXYLIC ACID has two methyl groups attached at positions 2 and 6 of the pyridine ring, and two carboxylic acid groups attached at positions 3 and 5. It is commonly used as a building block in the synthesis of pharmaceuticals and crop protection products. Additionally, it has potential applications in the field of coordination chemistry and as a ligand in metal complexation reactions.

Check Digit Verification of cas no

The CAS Registry Mumber 2602-36-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,6,0 and 2 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2602-36:
(6*2)+(5*6)+(4*0)+(3*2)+(2*3)+(1*6)=60
60 % 10 = 0
So 2602-36-0 is a valid CAS Registry Number.
InChI:InChI=1/C9H9NO4/c1-4-6(8(11)12)3-7(9(13)14)5(2)10-4/h3H,1-2H3,(H,11,12)(H,13,14)

2602-36-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,6-dimethylpyridine-3,5-dicarboxylic acid

1.2 Other means of identification

Product number -
Other names 2,6-Dimethyl-3,5-pyridinedicarboxylic 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:2602-36-0 SDS

2602-36-0Relevant articles and documents

Study of the acylation reaction of 2,6-dimethyl-3,5-pyridinedicarboxylic acid hydrazides

Nesterova,Voevudsky,Samukha,Zubatyuk,Shishkin

, p. 1511 - 1520 (2005)

Acylation of 3-ethoxycarbonyl-2,6-dimethyl-5-pyridinecarboxylic acid hydrazide and 2,6-dimethyl-3,5-pyridinedicarboxylic acid dihydrazide using aromatic acid chlorides gave the corresponding N-aroyl hydrazides. It was found that the hydrazinolysis of 3-ethoxycarbonyl-2,6-dimethyl-5-pyridine-dicarboxylic acid N-aroyl hydrazides occurred not at the ester group but as a rehydrazinolysis reaction at the dihydrazide fragment. 2005 Springer Science+Business Media, Inc.

Studies on ketene and its derivatives. LXXVI. Reactions of acetoacetamide and β aminocrotonamide with β diketone, β ketoaldehyde and related compounds

Kato,Noda

, p. 303 - 309 (2007/10/04)

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