150215-07-9 Usage
General Description
1,2,4-Thiadiazole-3-acetic acid, 5-[(ethoxycarbonyl)amino]-, methyl ester is a chemical compound that belongs to the class of organic compounds called thiadiazoles. The characteristic feature of thiadiazoles is a five-membered heterocyclic ring structure which contains two nitrogen atoms, one sulfur atom and two carbon atoms. In this particular compound, the thiadiazole ring is substituted at the 3rd position with an acetic acid group and at the 5th position with an (ethoxycarbonyl)amino group, and itself is a part of methyl ester group. The exact properties and potential uses or effects of this specific chemical are not widely reported in the literature, which is often the case with such specific compounds until they are studied for a specific application.
Check Digit Verification of cas no
The CAS Registry Mumber 150215-07-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,0,2,1 and 5 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 150215-07:
(8*1)+(7*5)+(6*0)+(5*2)+(4*1)+(3*5)+(2*0)+(1*7)=79
79 % 10 = 9
So 150215-07-9 is a valid CAS Registry Number.
InChI:InChI=1/C8H11N3O4S/c1-3-15-8(13)10-7-9-5(11-16-7)4-6(12)14-2/h3-4H2,1-2H3,(H,9,10,11,13)
150215-07-9Relevant articles and documents
A Practical Preparation of (Z)-2-(5-Amino-1,2,4-thiadiazol-3-yl)-2-(methoxyimino)acetic Acid
Tatsuta, Kuniaki,Miura, Shozo,Gunji, Hiroki,Tamai, Tetsuro,Yoshida, Ryonosuke,Inagaki, Takashi
, p. 6423 - 6426 (1993)
A Z-isomer of 2-(5-amino-1,2,4-thiadiazol-3-yl)-2-(methoxyimino)acetic acid, which is the common acyl moiety of clinically useful cephalosporins, has been prepared from the aminoisoxazols through the thiadiazol-acetate in two pathways.
Process for preparing 1,2,4-thiadiazole derivatives
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, (2008/06/13)
An improved process for the production of 5-amino-1,2,4-thiadiazol-3-yl-(2-(lower)-alkoxyimino)acetic acids starting from 5-substituted- or unsubstituted-3-amino-isoxazole compounds is disclosed herein. The title compounds are useful as acylating agents for the production of 7-acylaminocephalosporins.
