131864-71-6

  • Product Name:(S)-1-(2-CHLOROPHENYL) ETHANOL
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Product Details

Purity:99%

Fast Delivery Pharmaceutical Intermediates 131864-71-6 (S)-1-(2-CHLOROPHENYL) ETHANOL

  • Molecular Formula:C8H9ClO
  • Molecular Weight:156.612
  • Boiling Point:231.417 °C at 760 mmHg 
  • PKA:14.05±0.20(Predicted) 
  • Flash Point:93.758 °C 
  • PSA:20.23000 
  • Density:1.182 g/cm3 
  • LogP:2.39330 

(S)-1-(2-CHLOROPHENYL)ETHANOL(Cas 131864-71-6) Usage

Uses

It is an intermediate in organic syntheses and used as a pharmaceutical intermediates.

 

131864-71-6 Relevant articles

Enhancing cofactor regeneration of cyanobacteria for the light-powered synthesis of chiral alcohols

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, (2021/11/24)

Cyanobacteria Synechocystis sp. PCC 6803...

Cinchona-Alkaloid-Derived NNP Ligand for Iridium-Catalyzed Asymmetric Hydrogenation of Ketones

Zhang, Lin,Zhang, Ling,Chen, Qian,Li, Linlin,Jiang, Jian,Sun, Hao,Zhao, Chong,Yang, Yuanyong,Li, Chun

supporting information, p. 415 - 419 (2022/01/12)

Most ligands applied for asymmetric hydr...

Highly Active Cooperative Lewis Acid—Ammonium Salt Catalyst for the Enantioselective Hydroboration of Ketones

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supporting information, p. 5544 - 5553 (2021/02/05)

Enantiopure secondary alcohols are funda...

Tridentate nitrogen phosphine ligand containing arylamine NH as well as preparation method and application thereof

-

Paragraph 0095-0102; 0105-0109, (2021/06/26)

The invention discloses a tridentate nit...

131864-71-6 Process route

2-chlorostyrene
2039-87-4,107830-52-4,26125-41-7

2-chlorostyrene

(S)-1-(2'-chlorophenyl)ethanol
13524-04-4,120466-66-2,132437-66-2,131864-71-6

(S)-1-(2'-chlorophenyl)ethanol

2-(2-chlorophenyl)-1-ethanol
19819-95-5

2-(2-chlorophenyl)-1-ethanol

(R)-1-(o-chlorophenyl)ethanol
13524-04-4,131864-71-6,132437-66-2,120466-66-2

(R)-1-(o-chlorophenyl)ethanol

Conditions
Conditions Yield
2-chlorostyrene; With benzo[1,3,2]dioxaborole; rhodium complex 8; In toluene; at 20 ℃; for 2h;
With sodium hydroxide; water; dihydrogen peroxide; In toluene; at 20 ℃; for 2h; Title compound not separated from byproducts;
 
2-chlorostyrene; With bis(1,5-cyclooctadiene)rhodium(I) tetrafluoroborate; (1R,2R)-1,2-bis(di[2-furyl]phosphanyl)cyclohexane; benzo[1,3,2]dioxaborole; In 1,2-dimethoxyethane; toluene; at -75 ℃; for 1h;
With potassium hydroxide; dihydrogen peroxide; In 1,2-dimethoxyethane; Title compound not separated from byproducts;
 
With pinacol borane; 4 A molecular sieve; Rh(2,5-norbornadiene)2BF4; In 1,2-dimethoxyethane; at 20 ℃; for 12h; Title compound not separated from byproducts.;
 
2-chlorostyrene
2039-87-4,107830-52-4,26125-41-7

2-chlorostyrene

(S)-1-(2'-chlorophenyl)ethanol
13524-04-4,120466-66-2,132437-66-2,131864-71-6

(S)-1-(2'-chlorophenyl)ethanol

2-(2-chlorophenyl)-1-ethanol
19819-95-5

2-(2-chlorophenyl)-1-ethanol

(R)-1-(o-chlorophenyl)ethanol
13524-04-4,131864-71-6,132437-66-2,120466-66-2

(R)-1-(o-chlorophenyl)ethanol

Conditions
Conditions Yield
2-chlorostyrene; With benzo[1,3,2]dioxaborole; rhodium complex 8; In toluene; at 20 ℃; for 2h;
With sodium hydroxide; water; dihydrogen peroxide; In toluene; at 20 ℃; for 2h; Title compound not separated from byproducts;
 
2-chlorostyrene; With bis(1,5-cyclooctadiene)rhodium(I) tetrafluoroborate; (1R,2R)-1,2-bis(di[2-furyl]phosphanyl)cyclohexane; benzo[1,3,2]dioxaborole; In 1,2-dimethoxyethane; toluene; at -75 ℃; for 1h;
With potassium hydroxide; dihydrogen peroxide; In 1,2-dimethoxyethane; Title compound not separated from byproducts;
 
With pinacol borane; 4 A molecular sieve; Rh(2,5-norbornadiene)2BF4; In 1,2-dimethoxyethane; at 20 ℃; for 12h; Title compound not separated from byproducts.;
 

131864-71-6 Upstream products

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    2142-68-9

    1-(2-chlorophenyl)ethanone

  • 2039-87-4
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    2-chlorostyrene

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    vinyl acetate

  • 13524-04-4
    13524-04-4

    2'-chloro-sec-phenethyl alcohol

131864-71-6 Downstream products

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    929040-32-4

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    C21H16BrClN2O3S

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    5-(5-bromo-1H-benzimidazol-1-yl)-3-({(1R)-1-[2-chlorophenyl]ethyl}oxy)thiophene-2-carboxamide