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"Trans-4-(tert-butyl)cyclohexyl)(methyl)sulfane" is a chemical compound with the molecular formula C11H22S. It is a cyclic alkane with a sulfur atom bridging a methyl group and a tert-butyl group attached to a cyclohexane ring. The "trans" configuration indicates that the tert-butyl and methyl groups are positioned on opposite sides of the cyclohexane ring. (trans-4-(tert-butyl)cyclohexyl)(methyl)sulfane is an organosulfur compound, which means it contains carbon-sulfur bonds. It is a colorless liquid at room temperature and is used in various chemical reactions and as a reagent in organic synthesis. Due to its specific structure, it may have unique properties and reactivity compared to other similar compounds.

4934-66-1

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4934-66-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4934-66-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,9,3 and 4 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4934-66:
(6*4)+(5*9)+(4*3)+(3*4)+(2*6)+(1*6)=111
111 % 10 = 1
So 4934-66-1 is a valid CAS Registry Number.

4934-66-1Relevant academic research and scientific papers

Preparation of stereodefined secondary alkyllithium compounds

Seel, Stephanie,Dagousset, Guillaume,Thaler, Tobias,Frischmuth, Annette,Karaghiosoff, Konstantin,Zipse, Hendrik,Knochel, Paul

, p. 4614 - 4622 (2013/05/08)

We have developed a practical stereoretentive iodine/lithium-exchange process that allows the stereodefined preparation of cis- and trans-cycloalkyllithium compounds from their corresponding stereodefined iodides. Quenching with electrophiles offers stere

Metalation of 1,3-Dithiolanes. Mercaptan Synthesis and Carbonyl Transposition

Wilson, Stephen R.,Georgiadis, Gregory M.,Khatri, Hiralal N.,Bartmess, John E.

, p. 3577 - 3583 (2007/10/02)

The reaction of 1,3-dithiolanes with n-butyllithium results in fragmentation to the corresponding thiocarbonyl compound followed by furhter reaction with n-butyllithium.All four types of thiocarbonyl reactions are observed: reduction, S-addition, C-addition, double addition.Synthetic applications of this reaction for the synthesis of secondary mercaptans and 1,2-carbonyl transposition (23 -> 24a-c) are described.

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