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(4-methyl-[1,2,3]thiadiazol-5-yl)-carbamic acid phenyl ester is a complex organic compound with the chemical formula C10H8N2O2S2. It is a derivative of carbamic acid, featuring a phenyl ester group and a 4-methyl-[1,2,3]thiadiazol-5-yl moiety. (4-methyl-[1,2,3]thiadiazol-5-yl)-carbamic acid phenyl ester is characterized by its unique structure, which includes a thiadiazole ring and a phenyl group, making it a potential candidate for various chemical and pharmaceutical applications. Due to its specific functional groups and molecular structure, it may exhibit unique reactivity and properties that could be of interest in the synthesis of new compounds or as a building block in the development of pharmaceuticals. However, further research and characterization would be required to fully understand its potential uses and properties.

77196-90-8

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77196-90-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 77196-90-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,1,9 and 6 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 77196-90:
(7*7)+(6*7)+(5*1)+(4*9)+(3*6)+(2*9)+(1*0)=168
168 % 10 = 8
So 77196-90-8 is a valid CAS Registry Number.

77196-90-8Downstream Products

77196-90-8Relevant academic research and scientific papers

Process for making 5-mercapto-1,2,3-triazoles

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, (2008/06/13)

A process for making 5-mercapto-1,2,3-triazoles of the formula STR1 wherein R1 is hydrogen or a C1 -C4 -alkyl which may also be substituted, the said process comprising (1) as a first step reacting a solution of 1,2,3-thiadiazole-5-carbohydroxamic acid derivative of the formula STR2 wherein R1 has the meaning as above and R2 is hydrogen or a univalent metal equivalent in an inert organic solvent in the presence of an acid acceptor with a solution in an inert organic solvent of an acid halide of the formula so as to form an acylated 1,2,3-thiadiazole-5-carbohydroxamic acid derivative (2) reacting as a solution in an inert organic solvent the carbohydroxamic acid derivative just obtained with an alcohol or phenol of the formula so as to form a (1,2,3-thiadiazole-5-yl)-carbamic acid ester (3) then treating the thus obtained carbamic acid ester with an acetic or basic catalyst to form the 5-amino-1,2,3-thiadiazole (4) whereupon the said amino thiadiazole is subject to a rearrangement in the presence of a base followed by isolation of the product of the reaction.

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