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2-Propanol, 1-chloro-3-[(4-chlorophenyl)thio]-, also known as 1-chloro-3-(4-chlorophenylthio)-2-propanol, is an organic compound with the chemical formula C9H10Cl2OS. It is a colorless liquid with a molecular weight of 243.15 g/mol. 2-Propanol, 1-chloro-3-[(4-chlorophenyl)thio]- is characterized by the presence of a 2-propanol backbone, with a chlorine atom at the 1-position, a 4-chlorophenylthio group at the 3-position, and another chlorine atom attached to the phenyl ring. It is used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly in the production of fungicides. Due to its chemical structure, it may exhibit potential hazards, and appropriate safety measures should be taken during its handling and use.

2989-38-0

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2989-38-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2989-38-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,8 and 9 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2989-38:
(6*2)+(5*9)+(4*8)+(3*9)+(2*3)+(1*8)=130
130 % 10 = 0
So 2989-38-0 is a valid CAS Registry Number.

2989-38-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-chloro-3-(4-chlorophenyl)sulfanylpropan-2-ol

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:2989-38-0 SDS

2989-38-0Downstream Products

2989-38-0Relevant academic research and scientific papers

Recyclable superparamagnetic Fe3O4 nanoparticles for efficient catalysis of thiolysis of epoxides

Mojtahedi, Mohammad M.,Abaee, M. Saeed,Rajabi, Azam,Mahmoodi, Peyman,Bagherpoor, Saeed

experimental part, p. 68 - 71 (2012/08/07)

An efficient and rapid procedure is developed for room-temperature ring opening of various epoxides with thiols under solvent-free conditions in the presence of catalytic amount of superparamagnetic Fe3O4 nanoparticles. As a result,

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

Additive-free thiolysis of epoxides in water: A green and efficient regioselective pathway to β-hydroxy sulfides

Abaee, Saeed M.,Mojtahedi, Mohammad M.,Abbasi, Hassan,Fatemi, Ensieh R.

, p. 282 - 289 (2008/03/17)

Room-temperature ring opening of various epoxides with aromatic thiols was carried out in water in the absence of any Lewis acid or additive. High yields of β-hydroxy sulfides with excellent regioselectivity were obtained under very environmentally friend

Alumina-supported molybdenum (VI) oxide: An efficient and recyclable heterogeneous catalyst for regioselective ring opening of epoxides with thiols, acetic anhydride, and alcohols under solvent-free conditions

Singhal, Sweety,Jain, Suman L.,Sain, Bir

, p. 620 - 621 (2008/12/21)

An efficient and simple protocol for regioselective ring opening of epoxides with thiols, acetic anhydride, and alcohols using 16wt% MoO3 supported on alumina as a recyclable catalyst is described. Copyright

Facile room-temperature MgBr2·OEt2-catalyzed thiolysis of epoxides under solvent-free conditions

Mojtahedi, Mohammad M.,Abaee, M. Saeed,Bolourtchian, Mohammad,Abbasi, Hassan

, p. 905 - 910 (2008/02/01)

Solvent-free ring opening of 1,2-epoxides with aromatic and aliphatic thiols under 1 mol% magnesium bromide ethyl etherate catalysis affords rapid formation of β-hydroxy sulfides at ambient temperature with excellent yields. Nucleophilic attack of the thi

Stereo- and regioselective thiolysis of 1,2-epoxides in water

Movassagh, Barahman,Soleiman-Beigi, Mohammad

, p. 3239 - 3244 (2008/02/12)

A simple, efficient, stereoselective, and highly regioselective procedure for the synthesis of β-hydroxy sulfides by thiolysis of various 1,2-epoxides in water as a solvent, using no catalyst and under very mild conditions, is described. Copyright Taylor

Solvent-free thiolysis of epoxides under lithium perchlorate catalysis

Mojtahedi, Mohammad M.,Abassi, Hassan,Saeed Abaee,Mohebali, Bahareh

, p. 455 - 458 (2007/10/03)

Solvent-free ring opening of 1,2-epoxides with thiols using catalytic amounts of lithium perchlorate affords high yields of β-hydroxy sulfides. Nucleophilic attack of the thiols occurs regioselectively at the sterically less hindered side of the epoxides.

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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