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2,3,5,6-Pyridinetetracarboxylic acid, 1,4-dihydro-4-(3-nitrophenyl)-, tetraethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

60870-54-4

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60870-54-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 60870-54-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,8,7 and 0 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 60870-54:
(7*6)+(6*0)+(5*8)+(4*7)+(3*0)+(2*5)+(1*4)=124
124 % 10 = 4
So 60870-54-4 is a valid CAS Registry Number.

60870-54-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(3-nitro-phenyl)-1,4-dihydro-pyridine-2,3,5,6-tetracarboxylic acid tetraethyl ester

1.2 Other means of identification

Product number -
Other names tetraethyl 1,4-dihydro-4-(3-nitrophenyl)-2,3,5,6-pyridinetetracarboxylate

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:60870-54-4 SDS

60870-54-4Relevant academic research and scientific papers

4-(3-Nitrophenyl)-2,3,5,6-pyridinetetracarboxylic acid and intermediates

-

, (2008/06/13)

4-(3-Nitrophenyl)pyridine, an intermediate useful in the preparation of 1-(lower-alkyl)-1,4-dihydro-4-oxo-7-(4-pyridyl)-3-quinolinecarboxylates, which are useful as anti-bacterial agents, is prepared by reacting 3-nitrobenzaldehyde with two molar equivalents of di-lower-alkyl) oxalacetate (II) in the presence of a catalytic condensing agent, preferably piperidine and/or its acetate, to produce tetra-(lower-alkyl) 3-(3-nitrophenyl)-1,5-pentanedione-1,2,4,5-tetracarboxylate (III), reacting III with ammonia to produce tetra-(lower-alkyl) 1,4-dihydro-4-(3-nitrophenyl)-2,3,5,6-pyridinetetracarboxylate (IV), oxidizing IV to produce tetra-(lower-alkyl) 4-(3-nitrophenyl)-2,3,5,6-pyridinetetracarboxylate (V), hydrolyzing V to produce 4-(3-nitrophenyl)-2,3,5,6-pyridinetetracarboxylic acid (VI) and decarboxylating VI to produce 4-(3-nitrophenyl)pyridine (VII). Intermediates III, IV, V and VI are novel.

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