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82843-16-1

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82843-16-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 82843-16-1 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 6 respectively.
Calculate Digit Verification of CAS Registry Number 82843-16:
(7*8)+(6*2)+(5*8)+(4*4)+(3*3)+(2*1)+(1*6)=141
141 % 10 = 1
So 82843-16-1 is a valid CAS Registry Number.

82843-16-1SDS

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 2,4-dicyano-3-isobutyl-3-methylglutarimide

1.2 Other means of identification

Product number -
Other names 4-isobutyl-4-methyl-2,6-dioxo-piperidine-3,5-dicarbonitrile

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:82843-16-1 SDS

82843-16-1Downstream Products

82843-16-1Relevant articles and documents

Chemistry of 5,7-Dihydroxy-2H-thiopyranopyridine-4(3H)-one

Zigeuner, Gustav,Schweiger, Klaus,Schramm, Hans-Wolfgang

, p. 923 - 936 (2007/10/02)

Hydrolysis of the 4-alkyliminothiopyranopyridinedioles (5) and 4-alkylaminothiopyranopyridones (6) resp. with 10 percent NaOH gives 5,7-dihydroxy-2H-thiopyranopyridine-4(3H)-one (7). 7 can be obtained in better yield by reaction of 4-dimethylamino-2(1H)-pyridinethione (8) with bis-trichlorphenylethylmalonate (2).Aminolysis of 7 affords the two isomeric products 5 and 6.On treatment with hydrazines, 7 reacts only to 4-hydrazono-derivatives 5.By heating in bromobenzene 5d is cyclized to 1H-5,1,2,6-thiatriaza-acenaphthylen-7-ol (11).On methylation with methyliodide 5, 6 and 7 furnish the 7-methoxyproducts 13, 14 and 12.By heating in 20 percent NaOH 7 is transformed into the 2-thioxo-3-pyridylmethylketone 16A and its tautomer, 2-mercapto-3-pyridylmethylketone 16B.The structures of 5, 6 and 7 are discussed. - keywords: 4-Alkylaminothiopyranopyridones; 4-Alkyliminothiopyranopyridindioles; 5,7-Dihydroxy-2H-thiopyranopyridine-4(3H)-one; 2-Mercapto-3-pyridinylmethylketone; 1H-5,1,2,6-Thiatriaza-acenaphthylene; 2-Thioxo-3-pyridylmethylketone

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