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159583-29-6

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159583-29-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 159583-29-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,9,5,8 and 3 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 159583-29:
(8*1)+(7*5)+(6*9)+(5*5)+(4*8)+(3*3)+(2*2)+(1*9)=176
176 % 10 = 6
So 159583-29-6 is a valid CAS Registry Number.

159583-29-6SDS

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 1,2-dimethyldiazinan-4-amine

1.2 Other means of identification

Product number -
Other names 4-pyridazinamine,hexahydro-1,2-dimethyl

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:159583-29-6 SDS

159583-29-6Relevant articles and documents

Synthesis of p-aminobenzamides of aminopiperidazines as potential antiarrhythmic agents

Kornet,Abdul-Nabi Ali,Steinberg

, p. 967 - 971 (1994)

1,2-Dimethyl-4-aminopiperidazine (4), 1-(2-aminoethyl)-2-methylpiperidazine (11), 2-(2-aminoethyl)-3-methyl-2,3-diazabicyclo[2.2.1]heptane (16), and 1,2-dimethyl-3-aminomethylpiperidazine (21) have been synthesized. Amines 4, 11, and 16 were converted to the corresponding p-nitrobenzamides 7, 12, and 17. Catalytic reduction of the latter nitro derivatives gave the corresponding p-aminobenzamides 8, 13, and 18. For comparative studies, the acyclic analog, 4-amino-N-[2-(1,1,2-trimethylhydrazino)ethyl]benzamide (25) was also synthesized. Compounds 8, 13 and 25 which are analogs of procainamide were evaluated in the isolated cardiac Purkinje fiber preparation by measuring their effects on the action potential upstroke velocity.

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