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2-Propanol, 1-chloro-3-[(4-methylphenyl)thio]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

13708-10-6

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13708-10-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13708-10-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,7,0 and 8 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 13708-10:
(7*1)+(6*3)+(5*7)+(4*0)+(3*8)+(2*1)+(1*0)=86
86 % 10 = 6
So 13708-10-6 is a valid CAS Registry Number.

13708-10-6Downstream Products

13708-10-6Relevant academic research and scientific papers

An efficient catalyst for ring opening of epoxides with phenol and thiophenol under solvent-free conditions

Lu, Hong-Fei,Zhou, Jun-Tao,Cheng, He-Long,Sun, Lei-Lei,Yang, Fei-Fei,Wu, Run-Ze,Gao, Yu-Hua,Luo, Zhi-Bin

, p. 11174 - 11184 (2014/01/06)

An efficient and rapid procedure for ring opening reaction of various epoxides with phenol and thiophenol derivatives was developed. The procedure can be obtained at room temperature under solvent-free condition in presence of (C4H12N2)2[BiCl6] Cl·H2O (1 mol %). This catalyst can be reused several times without significant loss of activity.

Efficient synthesis of-Hydroxy sulfides and-Hydroxy sulfoxides catalyzed by Cu/MgO under solvent-free conditions

Das, Biswanath,Balasubramanyam, Penagaluri,Krishnaiah, Maddeboina,Veeranjaneyulu, Boyapati,Sudhakar, Dega

experimental part, p. 2113 - 2121 (2010/08/13)

Regio-, stereo-, and chemoselective ring opening of epoxides with thiols using Cu/MgO as a heterogeneous catalyst has efficiently been carried out to produce the corresponding β-hydroxy sulfides in excellent yields at room temperature under solvent-free c

Rongalite promoted highly regioselective synthesis of β-hydroxy sulfides by ring opening of epoxides with disulfides

Guo, Wenxue,Chen, Jiuxi,Wu, Dengze,Ding, Jinchang,Chen, Fan,Wu, Huayue

experimental part, p. 5240 - 5243 (2009/11/30)

Rongalite promotes cleavage of disulfides generating thiolate anions that then undergo facile ring opening of epoxides in the presence of K2CO3 to afford α-addition products 3 with good to excellent yields. The important f

Cyanuric chloride: An efficient catalyst for ring opening of epoxides with thiols under solvent-free conditions

Bandgar, Babasaheb P.,Joshi, Neeta S.,Kamble, Vinod T.,Sawant, Sanjay S.

, p. 231 - 234 (2008/09/18)

2,4,6-Trichloro-1,3,5-triazine-catalyzed convenient and efficient ring opening of epoxides with thiols under solvent-free conditions is described. Short reaction time, mild reaction conditions, inexpensive and readily available catalyst, and excellent yie

Highly regioselective ring opening of epoxides with thiols catalyzed by SbCl3 under solvent-free conditions

Ghazanfari, Dadkhoda,Hashemi, Mohammed M.,Akhgar, Mohammad Reza,Foroughi, Mohammad Mehdi,Najafi-Zadeh, Fariba

experimental part, p. 3018 - 3022 (2009/10/02)

The ring-opening reaction of epoxides with thiols by SbCl3 supported on Kieselguhr under solvent-free conditions, afforded high yields of β-hydroxy sulfides. Nucleophilic attack of the thiols occurs regioselectively at the less hindered side of the epoxid

Regioselective ring-opening reactions of 1,2-epoxides with thiols and arylselenols directly promoted by [Bmim]BF4

Yang, Ming-Hua,Yan, Guo-Bing,Zheng, Yun-Fa

supporting information; experimental part, p. 6471 - 6474 (2009/04/06)

Regioselective ring-opening reactions of 1,2-epoxides with ArSH and ArSeH promoted by ionic liquid [Bmim]BF4 were investigated. A variety of β-hydroxy selenides and β-hydroxy sulfides were obtained in excellent yields (81-99%) with good regiose

Lipase-catalyzed separation of the enantiomers of 1-substituted-3-arylthio- 2-propanols

Wielechowska, Monika,Plenkiewicz, Jan

, p. 1199 - 1205 (2007/10/03)

Optically active (R)- and (S)-1-substituted-3-(arylthio)propan-2-ols have been prepared in the reaction of the appropriate 2-(arylthiomethyl)oxiranes with chloride and azide anions followed by a lipase-catalyzed transesterification. The effects of the enzyme preparation as well as of the reaction conditions have been compared in terms of the enantiomeric excess of the obtained acetate and unreacted alcohol.

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