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1,4-dichloro-3,3,6,6-tetramethylpiperazine-2,5-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

57020-34-5

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57020-34-5 Usage

Chemical Class

Piperazine derivative

Structural Features

Two chlorine atoms
Four methyl groups attached to the piperazine ring
A cyclic diketone group

Mechanism of Action

Potent and selective Gardos channel blocker

Potential Applications

Anti-sickling activity
Anti-inflammatory activity

Target Conditions

Sickle cell disease
Other hemoglobinopathies
Inflammatory conditions

Research Status

Studied in preclinical trials

Current Stage

Further research and clinical trials needed to understand safety and efficacy

Potential as a Therapeutic Agent

May be developed for the treatment of the mentioned conditions if proven safe and effective

Check Digit Verification of cas no

The CAS Registry Mumber 57020-34-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,0,2 and 0 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 57020-34:
(7*5)+(6*7)+(5*0)+(4*2)+(3*0)+(2*3)+(1*4)=95
95 % 10 = 5
So 57020-34-5 is a valid CAS Registry Number.

57020-34-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,4-dichloro-3,3,6,6-tetramethylpiperazine-2,5-dione

1.2 Other means of identification

Product number -
Other names 2,5-Piperazinedione,1,4-dichloro-3,3,6,6-tetramethyl

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:57020-34-5 SDS

57020-34-5Downstream Products

57020-34-5Relevant academic research and scientific papers

Method of arresting bacterial growth with certain selected dichloro-2,2,5,5-tetrasubstituted-3-6-piperazinediones

-

, (2008/06/13)

There is provided, novel N-chloramine compounds of the 1,4-dichloro-2,2,5,5-tetrasubstituted-3,6-piperazinedione type, having the formula: STR1 WHERE R1, R2, R3, R4, which may be the same or different, each represent a member selected from the group consisting of an alkyl group of from 1 to 20 carbon atoms and an aryl group. The compounds encompassed by the above generic formula exhibit antibacterial activity, but most importantly, the compounds encompassed within the above generic formula exhibit enhanced stability over the closest related prior art compounds, when such compounds are employed in aqueous solution for antibacterial application.

N halo derivatives III: Stabilization of nitrogen chlorine bond in N chloroamino acid derivatives

Kaminski,Bodor,Higuchi

, p. 553 - 557 (2007/10/05)

The chlorination of α amino acids and their related derivatives was investigated. A kinetic study of the stability of these N chlorinated products led to an elucidation of the factors that significantly influence the stability and research of the nitrogen chlorine bond in these N chloramines. From the kinetic investigations, a series of low chlorine potential, soft antimicrobial N chloramines was developed based on derivatives of α aminoisobutyric acid and related compounds.

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