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(E)-1-Cyclohexyl-2-phenylsulfanyl-pent-3-en-1-ol is a complex organic compound characterized by a unique molecular structure. It features a cyclohexyl group attached to the first carbon, a phenylsulfanyl group at the second position, and a pent-3-en-1-ol chain, indicating a pentene with a hydroxyl group at the first carbon and a double bond between the third and fourth carbons. The "E" configuration specifies the geometric arrangement of the double bond, with the phenylsulfanyl group and the hydroxyl group on opposite sides of the double bond. (E)-1-Cyclohexyl-2-phenylsulfanyl-pent-3-en-1-ol is likely to have specific applications in the fields of chemistry and pharmaceuticals, given its intricate structure and potential for interaction with other molecules.

83877-47-8

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83877-47-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 83877-47-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,8,7 and 7 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 83877-47:
(7*8)+(6*3)+(5*8)+(4*7)+(3*7)+(2*4)+(1*7)=178
178 % 10 = 8
So 83877-47-8 is a valid CAS Registry Number.

83877-47-8Downstream Products

83877-47-8Relevant academic research and scientific papers

Selective Condensation of titanium Reagent with Carbonyl Compounds

Furuta, Kyoji,Ikeda, Yoshihiko,Meguriya, Noriyuki,Ikeda, Nobuo,Yamamoto, Hisashi

, p. 2781 - 2790 (2007/10/02)

titanium reagent generated easily from allyl ethyl sulfides condensed with aldehydes to give erythro-β-hydroxy sulfides in highly regio- and stereoselective manner.In contrast, crotyl ethyl sulfide reacted with aldehydes affording δ-hydroxy vinyl sulfide exclusively.The substitution pattern of the starting sulfide can have a pronounced effect on the selectivity in this condensation reaction, erythro-β-Hydroxy sulfide obtained was transfromed stereoselectively to the trans-vinyloxirane or 1,3-alkadiene.

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