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59573-44-3

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59573-44-3 Usage

General Description

(+)-(2S,5S)-2,5-dimethylpiperazine is a chemical compound with the molecular formula C6H14N2. It is a piperazine derivative, containing two methyl groups on the 2 and 5 positions of the piperazine ring. (+)-(2S,5S)-2,5-dimethylpiperazine is often used as a building block in the synthesis of pharmaceuticals and other organic compounds. It is a chiral molecule, meaning it has two different mirror image forms known as enantiomers. The (+)-(2S,5S) enantiomer of 2,5-dimethylpiperazine is the stereochemically pure form of the compound, with specific pharmacological and biological properties. Its structure and properties make it a versatile and important chemical in various industrial and research applications.

Check Digit Verification of cas no

The CAS Registry Mumber 59573-44-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,5,7 and 3 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 59573-44:
(7*5)+(6*9)+(5*5)+(4*7)+(3*3)+(2*4)+(1*4)=163
163 % 10 = 3
So 59573-44-3 is a valid CAS Registry Number.

59573-44-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (+)-(2S,5S)-2,5-dimethylpiperazine

1.2 Other means of identification

Product number -
Other names (S)-cis-2,5-Dimethyl-piperazin

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:59573-44-3 SDS

59573-44-3Relevant articles and documents

Reversible Interconversion between 2,5-Dimethylpyrazine and 2,5-Dimethylpiperazine by Iridium-Catalyzed Hydrogenation/Dehydrogenation for Efficient Hydrogen Storage

Fujita, Ken-Ichi,Wada, Tomokatsu,Shiraishi, Takumi

supporting information, p. 10886 - 10889 (2017/08/30)

A new hydrogen storage system based on the hydrogenation and dehydrogenation of nitrogen heterocyclic compounds, employing a single iridium catalyst, has been developed. Efficient hydrogen storage using relatively small amounts of solvent compared with previous systems was achieved by this new system. Reversible transformations between 2,5-dimethylpyrazine and 2,5-dimethylpiperazine, accompanied by the uptake and release of three equivalents of hydrogen, could be repeated almost quantitatively at least four times without any loss of efficiency. Furthermore, hydrogen storage under solvent-free conditions was also accomplished.

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