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76-96-0

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76-96-0 Usage

Uses

Methiotepa is a trifunctional aziridine chemosterilant.

Check Digit Verification of cas no

The CAS Registry Mumber 76-96-0 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 7 and 6 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 76-96:
(4*7)+(3*6)+(2*9)+(1*6)=70
70 % 10 = 0
So 76-96-0 is a valid CAS Registry Number.

76-96-0SDS

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 methiotepa

1.2 Other means of identification

Product number -
Other names tris(2-methyl-1-aziridinyl)phosphine sulfide

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:76-96-0 SDS

76-96-0Upstream product

76-96-0Downstream Products

76-96-0Relevant articles and documents

In the search for new anticancer drugs. 26. A comparison of anticancer activities of several TEPA, Thio-TEPA, Seleno-TEPA, and azetidine analogs, including congeners containing an aminoxyl moiety

Sosnovsky,Lukszo,Konieczny,Purgstaller,Laib

, p. 982 - 988 (1994)

A series of TEPA, Thio-TEPA, Seleno-TEPA, and azetidine analogs, including congeners containing an aminoxyl moiety, were synthesized and evaluated in vivo for anticancer activity against the murine lymphocytic leukemia P388. All aziridine derivatives were found to be active with an increase in life span ranging from 42% to 272%, and all azetidine analogs were rated as inactive with one marginal exception. An attempt was made to rationalize the results on the basis of the lipophilic properties of the compounds. The most active compound (8) possessed the most balanced lipophilic properties, corresponding to a log P value near zero.

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