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α-(3-Chlorphenyl)-N-(p-tolylsulfonylmethyl)-urethan is a complex organic compound with the chemical formula C15H14ClNO3S. It is a derivative of urea, featuring a 3-chlorophenyl group attached to the alpha carbon, a p-tolylsulfonylmethyl group connected to the nitrogen, and a sulfonyl group. α-<3-Chlorphenyl>-N--urethan is known for its potential applications in the synthesis of pharmaceuticals and agrochemicals due to its unique structural properties. It is a white crystalline solid that is sensitive to heat and moisture, and it is typically handled under controlled conditions to maintain its stability. The compound's specific reactivity and functional groups make it a valuable intermediate in the preparation of various chemical products.

3696-54-6

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3696-54-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3696-54-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,6,9 and 6 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 3696-54:
(6*3)+(5*6)+(4*9)+(3*6)+(2*5)+(1*4)=116
116 % 10 = 6
So 3696-54-6 is a valid CAS Registry Number.

3696-54-6Relevant academic research and scientific papers

Highly enantioselective monofluoromethylation of C2-arylindoles using FBSM under chiral phase-transfer catalysis

Matsuzaki, Kohei,Furukawa, Tatsuya,Tokunaga, Etsuko,Matsumoto, Takashi,Shiro, Motoo,Shibata, Norio

supporting information, p. 3282 - 3285 (2013/07/26)

The highly enantioselective addition of 1-fluoro-1,1-bis(phenylsulfonyl) methane (FBSM) to vinylogous imines generated in situ from 2-aryl-3-(1- arylsulfonylmethyl)indoles was achieved using chiral ammonium salts derived from cinchona alkaloids. One-pot c

InBr3: A versatile catalyst for the different types of Friedel-Crafts reactions

Thirupathi, Ponnaboina,Sung, Soo Kim

supporting information; experimental part, p. 7755 - 7761 (2009/12/27)

(Chemical Equation Presented) Mild and efficient InBr3-catalyzed Friedel-Crafts alkylation of heteroaromatic or electron-rich aromatic compounds with α-amido sulfones at room temperature in CH2Cl2 has been developed. The p

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