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22317-01-7

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22317-01-7 Usage

General Description

1,3-Dimethyl-piperazine is a chemical compound with the molecular formula C6H14N2 and a structure that consists of a six-membered ring containing two nitrogen atoms and two methyl groups attached to one of the nitrogen atoms. It is a colorless liquid with a mild, amine-like odor that is used primarily as a building block in the synthesis of pharmaceuticals and agrochemicals. The compound is also used as a corrosion inhibitor and as an intermediate in the production of polymers and surfactants. Additionally, 1,3-dimethyl-piperazine has been investigated for its potential use as a solvent in carbon capture and storage applications due to its ability to absorb carbon dioxide. It is considered to be relatively low in toxicity and is not classified as a hazardous substance by regulatory agencies.

Check Digit Verification of cas no

The CAS Registry Mumber 22317-01-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,3,1 and 7 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 22317-01:
(7*2)+(6*2)+(5*3)+(4*1)+(3*7)+(2*0)+(1*1)=67
67 % 10 = 7
So 22317-01-7 is a valid CAS Registry Number.

22317-01-7SDS

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 1,3-Dimethylpiperazine

1.2 Other means of identification

Product number -
Other names 1,3-dimethyl-piperazine

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:22317-01-7 SDS

22317-01-7Relevant articles and documents

Biocatalytic Access to Piperazines from Diamines and Dicarbonyls

Borlinghaus, Niels,Gergel, Sebastian,Nestl, Bettina M.

, p. 3727 - 3732 (2018/04/14)

Given the widespread importance of piperazines as building blocks for the production of pharmaceuticals, an efficient and selective synthesis is highly desirable. Here we show the direct synthesis of piperazines from 1,2-dicarbonyl and 1,2-diamine substrates using the R-selective imine reductase from Myxococcus stipitatus as biocatalyst. Various N- and C-substituted piperazines with high activity and excellent enantioselectivity were obtained under mild reaction conditions reaching up to 8.1 g per liter.

Studies in Potential Filaricides: Part 20 - Synthesis of 1,4-Disubstituted Piperazines as Diethylcarbamazine Analogs

Charles, Elisabeth S.,Sharma, Satyavan

, p. 752 - 756 (2007/10/02)

A series of substituted 2,4-dimethylpiperazines (10-15), 1-benzyl-2-methylpiperazines (16-19), 1-substituted 3-methylpiperazines (20-25,27) and 1,4-disubstituted piperazines (28-34) have been synthesized starting from 1-benzyl-2-methylpiperazine (9) and 1

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