57-39-6 Usage
Chemical Properties
Amber liquid; amine odor. Miscible with water and organic
solvents.
Uses
Different sources of media describe the Uses of 57-39-6 differently. You can refer to the following data:
1. Chemosterilant; in creaseproofing and flameproofing textiles.
2. Metepa is a chemosterilant.
Hazard
Toxic by ingestion and skin absorption,
strong irritant to skin.
Safety Profile
Poison by ingestion,
skin contact, intraperitoneal, and
subcutaneous routes. Experimental
teratogenic and reproductive effects.
Questionable carcinogen with experimental
carcinogenic data. Animal experiments
suggest cholinesterase inlubition, possibly
due to metabolic products of this material in
the body. When heated to decomposition it
emits very toxic fumes of NOx and POx.
Check Digit Verification of cas no
The CAS Registry Mumber 57-39-6 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 5 and 7 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 57-39:
(4*5)+(3*7)+(2*3)+(1*9)=56
56 % 10 = 6
So 57-39-6 is a valid CAS Registry Number.
InChI:InChI=1/C5H10NOP/c1-4-5(2,3)6(4)8-7/h4H,1-3H3
57-39-6Relevant 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 (2007/10/02)
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.