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(E)-1-Cyclohexyl-4-ethylsulfanyl-3-methyl-but-3-en-1-ol is a complex organic compound characterized by its unique structure and properties. It features a cyclohexyl group attached to the first carbon, an ethylsulfanyl group at the fourth carbon, and a methyl group at the third carbon of a but-3-en-1-ol backbone. The "E" configuration indicates that the double bond has a trans arrangement, meaning the substituents on the double bond are on opposite sides. (E)-1-Cyclohexyl-4-ethylsulfanyl-3-methyl-but-3-en-1-ol is likely to be found in the realm of specialty chemicals, potentially used in the synthesis of pharmaceuticals, fragrances, or other industrial applications due to its specific functional groups and structural features.

83877-57-0

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83877-57-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 83877-57-0 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 7 respectively.
Calculate Digit Verification of CAS Registry Number 83877-57:
(7*8)+(6*3)+(5*8)+(4*7)+(3*7)+(2*5)+(1*7)=180
180 % 10 = 0
So 83877-57-0 is a valid CAS Registry Number.

83877-57-0Downstream Products

83877-57-0Relevant 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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