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N-Butyl-S-methyl-N'-tosyl-isothioharnstoff, also known as N-butyl-S-methyl-N'-tosyl-isothiourea, is an organic compound with the chemical formula C12H20N2OS2. It is a derivative of isothiourea, featuring a butyl group, a methyl group, and a tosyl group (tosyl is a toluene sulfonate group). N-Butyl-S-methyl-N'-tosyl-isothioharnstoff is primarily used as a reagent in organic synthesis, particularly in the formation of carbon-nitrogen bonds. It is known for its ability to act as a protecting group in certain chemical reactions, which can be crucial for the selective synthesis of complex molecules. The compound's structure and properties make it a valuable tool in the field of organic chemistry, although it should be handled with care due to its potential reactivity and toxicity.

960-35-0

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960-35-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 960-35-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,6 and 0 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 960-35:
(5*9)+(4*6)+(3*0)+(2*3)+(1*5)=80
80 % 10 = 0
So 960-35-0 is a valid CAS Registry Number.

960-35-0Relevant academic research and scientific papers

SYNTHESIS AND PROPERTIES OF N3-SUBSTITUTED N1,N2-BISARYLSULFONYLGUANIDINES

Dubina, V. L.,Dobronravov, A. N.

, p. 1731 - 1734 (2007/10/02)

N3-Substituted N1,N2-bisarylsulfonylguanidines were obtained by the amidation of derivatives of N-arylsulfonylcarbonimidic acid.Their structural similarity to butamide (N1-p-tolylsulfonyl-N2-butylurea) and cyclamide (N1-p-tolylsulfonyl-N2-cyclohexylurea) and also the similarity of some their chemical characteristics are not determining factors in the manifestation of sugar-decreasing characteristics by these guanidine derivatives.

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