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Cyclohexanol, 2-(ethylthio)-, (1R,2S)-rel- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

613258-12-1

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613258-12-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 613258-12-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,1,3,2,5 and 8 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 613258-12:
(8*6)+(7*1)+(6*3)+(5*2)+(4*5)+(3*8)+(2*1)+(1*2)=131
131 % 10 = 1
So 613258-12-1 is a valid CAS Registry Number.

613258-12-1Downstream Products

613258-12-1Relevant academic research and scientific papers

Lanthanide-based coordination polymers as promising heterogeneous catalysts for ring-opening reactions

Kumar, Gulshan,Kumar, Girijesh,Gupta, Rajeev

, p. 21352 - 21361 (2016/03/08)

This work presents the synthesis and structural characterization of Eu3+- and Tb3+-based coordination polymers starting from a Co3+-based metalloligand offering appended arylcarboxylic acid groups. Both coordination polymers function as reusable heterogeneous catalysts for ring-opening reactions utilizing amines, alcohols, thiols, and azides as the nucleophiles. The catalytic results illustrate an excellent control over the regioselectivity whereas a filtration test and mechanistic studies substantiate Lewis-acid catalyzed activation of the epoxide during the reaction.

Chemical oxidation studies of β-hydroxysulfides with tris(4-bromophenyl)aminium hexachloroantimonate: Diastereoselective sulfoxide obtaining and pinacol-type rearrangement

Donnici, Claudio Luis,Guimaraes, Sibele,De Melo, Angelita Cristine

, p. 1489 - 1497 (2007/10/03)

The chemical oxidation of some β-hydroxy-sulfides in the presence of tris(4-bromo-phenyl)aminium hexachloroantimonate (TBPA) is reported. The oxidation of 2-ethylsulfanyl-cyclohexan-1-ol (cis- and trans-) resulted the corresponding sulfoxides with good diastereoselectivity (d.e. 50%) and for 2-methyl-2-ethylsulfanyl-cyclohexan-1-ol and 2-ethylsulfanyl-1,2-diphenyl-ethanol, the corresponding nonsulfanylated ketones (61-75%) and ethyl ethanethiolsulfonate (51-65%) were obtained via oxidative cleavage and pinacol-type rearrangement.

THE CHEMISTRY OF α,ω-MERCAPTOALCOHOLS IN THE PRESENCE OF DIETHOXYTRIPHENYLPHOSPHORANE. TEMEPERATURE DEPENDENCE OF CYCLODEHYDRATIONS AND S-ETHYLATIONS

Robinson, Philip L.,Kelly, Jeffery W.,Slayton, A. Evans

, p. 59 - 70 (2007/10/02)

Diethoxytriphenylphosphorane (DTPP) is easily prepared by oxidative addition of triphenylphosphine with diethyl peroxide.DTPP converts a variety of mercaptoalcohols to cyclic sulfides as well as hydroxythioethers.The temperature dependence (+25 --> -25 deg C) of the product distribution has synthetic petential.

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