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1428-92-8

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1428-92-8 Usage

Synonyms

4-BCP, nitrogen mustard analogue

Chemical class

Alkylating agent

Structure

Piperazine derivative with two chloroethyl groups

Function

Used in the synthesis of antineoplastic agents

Target

Cross-links DNA, leading to cell death

Potential treatments

Various cancers, including lymphoma and leukemia

Mechanism of action

Inhibits cell growth and induces apoptosis in cancer cells

Toxicity

Highly toxic

Safety precautions

Handle and use with caution in laboratory and medical settings

Adverse effects

Can cause serious side effects due to its toxicity

Check Digit Verification of cas no

The CAS Registry Mumber 1428-92-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,2 and 8 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1428-92:
(6*1)+(5*4)+(4*2)+(3*8)+(2*9)+(1*2)=78
78 % 10 = 8
So 1428-92-8 is a valid CAS Registry Number.

1428-92-8SDS

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-bis(2-chloroethyl)piperazine,dihydrochloride

1.2 Other means of identification

Product number -
Other names -

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:1428-92-8 SDS

1428-92-8Relevant articles and documents

Design and Synthesis of RNA-Specific Groove-Binding Cations: Implications for Antiviral Drug Design

McConnaughie, Adrian W.,Spychala, Jaroslaw,Zhao, Min,Boykin, David,Wilson, W. David

, p. 1063 - 1069 (1994)

As as initial step in the design of structure-specific RNA-interactive molecules as potential antiviral agents, we have focused on the synthesis of molecules that exhibit strong and preferential binding to douplex RNA.A series of polycationic ligands have

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