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Cyclohexane, 1-chloro-2-(methylthio)-, trans- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

41578-06-7

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41578-06-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 41578-06-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,5,7 and 8 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 41578-06:
(7*4)+(6*1)+(5*5)+(4*7)+(3*8)+(2*0)+(1*6)=117
117 % 10 = 7
So 41578-06-7 is a valid CAS Registry Number.

41578-06-7Relevant academic research and scientific papers

A facile sulfenylchlorination of alkenes with Me2SO/(COCl)2

Lan, Liyuan,Gao, Yang,Ding, Rui,Zhang, Ting,Liu, Yongguo,Sun, Baoguo,Tian, Hongyu

supporting information, p. 539 - 549 (2019/02/01)

The sulfenylchlorination of a series of alkenes is investigated by using the combined reagent of dimethyl sulfoxide and oxalyl chloride. The corresponding β-chloro sulfides were obtained in mediate to good yields. Most of the terminal alkenes give the Mar

Metal-Free Chlorothiolation of Alkenes Using HCl and Sulfoxides

Ebule, Rene,Hammond, Gerald B.,Xu, Bo

supporting information, p. 4705 - 4708 (2018/09/06)

We report a novel method for the chlorothiolation of alkenes using HCl and sulfoxides to achieve the 1,2-difunctionalization of unactivated alkenes. The combination of our new HCl reagent (HCl/DMPU) with sulfoxides forms a unique chlorothiolation system.

A Facile Method for the Sulfenyllactonization of Alkenoic Acids Using Dimethyl Sulfoxide Activated by Oxalyl Chloride

Zhang, Ting,Dai, Yifeng,Cheng, Siwei,Liu, Yongguo,Yang, Shaoxiang,Sun, Baoguo,Tian, Hongyu

, p. 1380 - 1386 (2017/03/11)

A simple approach has been developed for the sulfenyllactonization of alkenoic acids using dimethyl sulfoxide activated with oxalyl chloride, in which methanesulfenyl chloride is proposed as the intermediate.

Conformational analysis of 1-Y, 2-Z-cyclohexanes ( Y = OH, OMe, F, Cl, Br and I; Z= SMe, SOMe and SO2Me): Study of the Z/Y gauche interactions

Carreno,Carretero,Garcia Ruano,Rodriguez

, p. 5649 - 5664 (2007/10/02)

The conformational study of the title compounds is reported. The configurational assignment of the epimeric sulfoxides was based on the relationship between the stereochemistry of the sulfinyl group and the chemical shifts of the neighboring nuclei. The v

A FACILE METHOD FOR THE SYNTHESIS OF β-CHLOROALKYL SULFIDES USING DIMETHYL SULFOXIDE ACTIVATED BY PHENYL DICHLOROPHOSPHATE OR PHOSPHORUS OXYCHLORIDE

Liu, Hsing-Jang,Nyangulu, James M.

, p. 5467 - 5470 (2007/10/02)

A simple procedure has been developed for the transformation of alkenes to β-chloroalkyl sulfides using dimethyl sulfoxide activated with phenyl dichlorophosphate or phosphorus oxychloride.

BEHAVIOR OF CYCLOALKENES IN SULFENYLCHLORINATION-DEHYDROCHLORINATION REACTIONS

Gritsenko, E. I.,Butenko, G. G.,Plemenkov, V. V.

, p. 673 - 678 (2007/10/02)

By the addition of alkanesulfenyl chlorides to cyclohexene, cyclopentene, indene, and 7-oxabenzonorbornadiene the corresponding β-chlorocycloalkyl alkyl sulfides were obtained.They were subsequently investigated in elimination reactions with alkali-metal

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