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82843-18-3

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82843-18-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 82843-18-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,8,4 and 3 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 82843-18:
(7*8)+(6*2)+(5*8)+(4*4)+(3*3)+(2*1)+(1*8)=143
143 % 10 = 3
So 82843-18-3 is a valid CAS Registry Number.

82843-18-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-ethyl-4-hydroxy-1,7,7-trimethyl-5-sulfanylidene-6,8-dihydro-1,6-naphthyridin-2-one

1.2 Other means of identification

Product number -
Other names 3-ethyl-2-hydroxy-1,7,7-trimethyl-5-sulfanylidene-6,8-dihydro-1,6-naphthyridin-4-one

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:82843-18-3 SDS

82843-18-3Downstream Products

82843-18-3Relevant articles and documents

Reaction of 4-Alkylaminodihydro-2(1H)-pyridinethions and -ones resp. with Bis-trichlorophenyl-ethylmalonate

Zigeuner, Gustav,Schweiger, Klaus,Habernig, Dietmar

, p. 573 - 582 (2007/10/02)

4-Alkylamino-2(1H)-pyridinethiones (1) react with bis-trichlorophenyl-ethylmalonate (3) to give four isomeric products: 5-thioxo-1,6-naphthyridine-2(1H)-ones (4), 7,7-dimethyl-4H-thiopyranopyridine-4-ones (6), 2,2-dimethyl-2H-thiopyranopyridine-5,7-dioles (7) and 2,2-dimethyl-2H-thiopyranopyridine-5(3H)-ones (8).On treatment with alkali the thioxogroup of 4 is hydrolyzed and 1,6-naphthyridinediones (5) are formed.Compound 5 can also be synthesized by heating the alkylaminopyridones (2) together with 3. 6 can be hydrolyzed to 2-thioxo-3-pyridylprop ylketones (12).On treatment with diluted alkali or conc. acid the aminogroup of 7 and 8 is hydrolyzed and 10 is formed.By heating in 20percent NaOH 10 is transformed to the dihydroxymercapto-3-pyridylmethylketone (11). - Keywords: 4-alkylaminodihydro-2(1H)pyridinthiones and -ones; Bis-trichlorphenylmalonate; 2H-Thiopyranopyridine-5,7-dioles; 4H-Thiopyranopyridine-4-ones; 2H-Thiopyranopyridine-5-ones; 5-Thioxo-1,6-naphthyridine-2(1H)-ones

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