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98267-09-5

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98267-09-5 Usage

Type of compound

Aziridine derivative

Structural feature

Contains a quinoline sulfonyl group

Potential use

Antitumor agent

Activity

Exhibits cytotoxic activity against various cancer cell lines in vitro

Mechanism of action

Inhibits tubulin polymerization

Additional effect

Induces apoptosis in cancer cells

Current status

Research is ongoing

Goal

Developing it into a novel chemotherapy agent for treating cancer

Check Digit Verification of cas no

The CAS Registry Mumber 98267-09-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,2,6 and 7 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 98267-09:
(7*9)+(6*8)+(5*2)+(4*6)+(3*7)+(2*0)+(1*9)=175
175 % 10 = 5
So 98267-09-5 is a valid CAS Registry Number.

98267-09-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-(aziridin-1-ylsulfonyl)-8-methoxyquinoline

1.2 Other means of identification

Product number -
Other names N-(8-methoxy-5-quinolylsulfonyl)aziridine

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:98267-09-5 SDS

98267-09-5Downstream Products

98267-09-5Relevant articles and documents

SYNTHESIS OF N-(8-METHOXY-5-QUINOLYLSULFONYL)AZIRIDINE AND ITS REACTIONS WITH SECONDARY AMINES. PMR SPECTRA AND STRUCTURES OF THE DERIVATIVES OBTAINED

Gracheva, I. N.,Prokof'ev, E. P.,Kovel'man, I. R.,Tochilkin, A. I.

, p. 887 - 891 (1985)

A method for the synthesis of a new fluorescent derivative of ethyleneimine, viz., N-(8-methoxy-5-quinolylsulfonyl)-aziridine, starting from 8-methoxyquinoline-5-sulfonyl chloride was developed.The quinolylsulfonylaziridine reacts smoothly with secondary aliphatic amines to give 8-methoxy-5-quinolinesulfonamides.In a study of the PMR spectra of these compounds it was established that significant deshielding of the 4-H proton (0.8 ppm) and a substantial increase (by 0.8 ppm) in 3J(6,7) are characteristic signs of the introduction of aziridinylsulfonyl or N-(2-N-dialkylamino)sulfonamido substituents into the 5 position of 8-methoxyquinoline.

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