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90942-23-7

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90942-23-7 Usage

Chemical class

Piperazine derivatives

Functionality

Bifunctional alkylating agent

Applications

a. Synthesis of pharmaceutical compounds
b. Synthesis of organic molecules
c. Cross-linking polymers and proteins
d. Potential drug delivery system
e. Precursor for antitumor agents

Structural features

a. Two bromoethyl groups attached to the piperazine ring

Importance

a. Building block in organic synthesis
b. Building block in medicinal chemistry

Safety concerns

a. Potential cytotoxicity
b. Potential mutagenicity
c. Caution required in handling

Check Digit Verification of cas no

The CAS Registry Mumber 90942-23-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,9,4 and 2 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 90942-23:
(7*9)+(6*0)+(5*9)+(4*4)+(3*2)+(2*2)+(1*3)=137
137 % 10 = 7
So 90942-23-7 is a valid CAS Registry Number.

90942-23-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,4-bis(2-bromoethyl)piperazine,hydrobromide

1.2 Other means of identification

Product number -
Other names 1,4-Bis-(2-brom-aethyl)-piperazin,Dihydrobromid

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:90942-23-7 SDS

90942-23-7Relevant articles and documents

Synthesis and cytotoxicity of novel bisellipticines and bisisoellipticines

Obaza-Nutaitis, Judy A.,Gribble, Gordon W.

, p. 171 - 187 (2019/07/31)

A series of bis-ellipticines 7-9 and bis-isoellipticines 10-12 tethered through the indole nitrogen was synthesized and screened for antitumor cytotoxicity in the L-1210 murine leukemia assay. Activity was only displayed by 1,10-bis(6-ellipticinyl)-?-decane (8).

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