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144476-58-4

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  • 3,5-Pyridinedicarboxylic acid, 2,6-dimethyl-4-(4-nitrophenyl)-, 2-methoxyethyl 1-methylethyl ester

    Cas No: 144476-58-4

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144476-58-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 144476-58-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,4,4,7 and 6 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 144476-58:
(8*1)+(7*4)+(6*4)+(5*4)+(4*7)+(3*6)+(2*5)+(1*8)=144
144 % 10 = 4
So 144476-58-4 is a valid CAS Registry Number.

144476-58-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,6-Dimethyl-4-(4-nitro-phenyl)-pyridine-3,5-dicarboxylic acid 3-isopropyl ester 5-(2-methoxy-ethyl) ester

1.2 Other means of identification

Product number -
Other names -

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

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More Details:144476-58-4 SDS

144476-58-4Upstream product

144476-58-4Downstream Products

144476-58-4Relevant articles and documents

Polarographic study of the photodecomposition of nimodipine

Zanocco,Diaz,Lopez,Nunez-Vergara,Squella

, p. 920 - 924 (1992)

Nimodipine, a calcium antagonist belonging to the dihydropyridine family, produces a well-defined polarographic peak due to the four-electron reduction of the nitro group. This peak was used to track the photodecomposition of nimodipine induced by UV light and daylight. Nimodipine was modified by UV irradiation with degradation following first-order kinetics. A degradation rate constant of 0.099 min-1, with a half-life of 7.78 min, for UV irradiation without a filter was obtained. Furthermore, a quantum yield of 1.32 x 10-3 molecules/quantum absorbed was measured with a chemical actinometer. The UV degradation product, which was isolated and identified, showed that irradiation of nimodipine causes oxidation of the dihydropyridine ring and transmutation of the nitro group in the nitrobenzene moiety.

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