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(E)-1-Cyclohexyl-3-methyl-4-phenylsulfanyl-but-3-en-1-ol is a complex organic compound with a molecular formula of C19H26OS. It features a cyclohexyl group, a methyl group, a phenylsulfanyl group, and a but-3-en-1-ol moiety. The "E" configuration indicates that the double bond has a trans arrangement of substituents. (E)-1-Cyclohexyl-3-methyl-4-phenylsulfanyl-but-3-en-1-ol is characterized by its unique structure, which includes a cyclohexane ring, an alkenyl chain with a sulfur atom bonded to a phenyl group, and a hydroxyl group. It is an example of a chiral molecule, meaning it has non-superimposable mirror images, and it is used in various chemical and pharmaceutical applications due to its specific stereochemistry and functional groups.

83877-56-9

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83877-56-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 83877-56-9 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, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 83877-56:
(7*8)+(6*3)+(5*8)+(4*7)+(3*7)+(2*5)+(1*6)=179
179 % 10 = 9
So 83877-56-9 is a valid CAS Registry Number.

83877-56-9Downstream Products

83877-56-9Relevant 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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