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3-phenyltetrahydro-2H-thiopyran 1,1-dioxide is a chemical compound with the molecular formula C11H13O2S. It is a derivative of tetrahydrothiopyran, featuring a phenyl group attached to the 3-position and a sulfone group (-SO2) at the 1,1-position. 3-phenyltetrahydro-2H-thiopyran 1,1-dioxide is an organic sulfur-containing molecule, which can be used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds. Its structure provides a unique combination of aromatic, aliphatic, and sulfur-containing functional groups, making it a versatile building block in organic synthesis. The compound is typically synthesized through various chemical reactions, such as the reaction of phenylmagnesium bromide with 3-chlorotetrahydrothiopyran 1,1-dioxide, followed by oxidation. Due to its complex structure and potential applications, 3-phenyltetrahydro-2H-thiopyran 1,1-dioxide is of interest to researchers in the fields of organic chemistry and medicinal chemistry.

6581-68-6

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6581-68-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6581-68-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,5,8 and 1 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6581-68:
(6*6)+(5*5)+(4*8)+(3*1)+(2*6)+(1*8)=116
116 % 10 = 6
So 6581-68-6 is a valid CAS Registry Number.

6581-68-6Downstream Products

6581-68-6Relevant academic research and scientific papers

Enantioselective synthesis of chiral sulfones by ir-catalyzed asymmetric hydrogenation: A facile approach to the preparation of chiral allylic and homoallylic compounds

Zhou, Taigang,Peters, Byron,Maldonado, Matias F.,Govender, Thavendran,Andersson, Pher G.

, p. 13592 - 13595 (2012/10/08)

A highly efficient and enantioselective Ir-catalyzed hydrogenation of unsaturated sulfones was developed. Chiral cyclic and acyclic sulfones were produced in excellent enantioselectivities (up to 98% ee). Coupled with the Ramberg-Baecklund rearrangement, this reaction offers a novel route to chiral allylic and homoallylic compounds in excellent enantioselectivities (up to 97% ee) and high yields (up to 94%).

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