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Cyclohexanesulfinic acid is an organic compound with the chemical formula C6H11SO2H. It is a cyclic sulfinic acid, featuring a cyclohexane ring with a sulfinyl group (-SO2H) attached to one of the carbon atoms. Cyclohexanesulfinic acid is known for its unique reactivity and stability, which makes it a valuable intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. Cyclohexanesulfinic acid can be prepared through various methods, including the reaction of cyclohexanone with sodium sulfite or the oxidation of cyclohexyl methyl sulfide. Its applications span across different industries, highlighting its importance in chemical research and development.

5675-01-4

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5675-01-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5675-01-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,7 and 5 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 5675-01:
(6*5)+(5*6)+(4*7)+(3*5)+(2*0)+(1*1)=104
104 % 10 = 4
So 5675-01-4 is a valid CAS Registry Number.

5675-01-4Relevant academic research and scientific papers

Direct Substitution of Secondary and Tertiary Alcohols to Generate Sulfones under Catalyst- and Additive-Free Conditions

Liu, Yanan,Xie, Peizhong,Sun, Zuolian,Wo, Xiangyang,Gao, Cuiqing,Fu, Weishan,Loh, Teck-Peng

, p. 5353 - 5356 (2018/09/13)

An environmentally benign protocol that affords propargylic sulfones containing highly congested carbon centers from easily accessible alcohols and sulfinic acids with water as the only byproduct is reported. The reaction proceeded via an in situ dehydrative cross-coupling process by taking advantage of the synergetic actions of multiple hydrogen bonds rather than relying on an external catalyst and/or additives to achieve high product distribution.

Mercury-Photosensitized Sulfination, Hydrosulfination, and Carbonylation of Hydrocarbons: Alkane and Alkene Conversion to Sulfonic Acids, Ketones, and Aldehydes

Ferguson, Richard R.,Crabtree, Robert H.

, p. 5503 - 5510 (2007/10/02)

Mercury-photosensitized sulfination of alkanes, RH, with SO2 forms sulfinic acids (RSOOH) and sulfinate esters (RSOOR) in high conversion and yield; oxidation of the mixture produces RSO2OH in high yield.Mercury-photosensitized hydrosulfination of alkenes with H2 and SO2 gives RSO2OH after oxidative workup.Mercury-photosensitized carbonylation of alkanes with CO gives RCHO and R2CO.

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