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171032-87-4

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

Purity:99%

Industrial grade (S)-1-(2-FLUOROPHENYL)ETHANOL 171032-87-4 with Best Price

  • Molecular Formula:C8H9 F O
  • Molecular Weight:140.157
  • Vapor Pressure:0.297mmHg at 25°C 
  • Boiling Point:193℃ 
  • PKA:13.95±0.20(Predicted) 
  • Flash Point:88℃ 
  • PSA：20.23000 
  • Density:1.123 
  • LogP:1.87900 

(S)-1-(2-FLUOROPHENYL)ETHANOL(Cas 171032-87-4) Usage

Uses

(S)-1-(2-FLUOROPHENYL)ETHANOL is a building block used in organic synthesis such as JN403, a novel nicotinic acetylcholine receptor α7 agonist.

InChI:InChI=1/C8H9FO/c1-6(10)7-4-2-3-5-8(7)9/h2-6,10H,1H3/t6-/m0/s1

171032-87-4 Relevant articles

Biocatalytic reduction of ketones by a semi-continuous flow process using supercritical carbon dioxide

Matsuda, Tomoko,Watanabe, Kazunori,Kamitanaka, Takashi,Harada, Tadao,Nakamura, Kaoru

, p. 1198 - 1199 (2003)

The immobilized resting-cell of Geotrich...

Novel non-metal catalyst for catalyzing asymmetric hydrogenation of ketone and alpha, beta-unsaturated ketone

-

Paragraph 0144-0149, (2021/04/26)

The invention discloses a novel non-meta...

Arene-Immobilized Ru(II)/TsDPEN Complexes: Synthesis and Applications to the Asymmetric Transfer Hydrogenation of Ketones

Doherty, Simon,Knight, Julian G.,Alshaikh, Hind,Wilson, James,Waddell, Paul G.,Wills, Corinne,Dixon, Casey M.

supporting information, p. 226 - 235 (2020/12/31)

The Noyori-Ikariya (arene)Ru(II)/TsDPEN ...

171032-87-4 Process route

1-(2-fluorophenyl)ethanol
445-26-1

1-(2-fluorophenyl)ethanol

2'-Fluoroacetophenone
445-27-2

2'-Fluoroacetophenone

(1S)-1-(2-fluorophenyl)ethanol
171032-87-4

(1S)-1-(2-fluorophenyl)ethanol

(R)-1-(2-fluorophenyl)ethanol
162427-79-4

(R)-1-(2-fluorophenyl)ethanol

Conditions
Conditions Yield
With Arthrobacter atrocyaneus; In N,N-dimethyl-formamide; at 32 ℃; for 48h; Microbiological reaction;
 
2'-Fluoroacetophenone
445-27-2

2'-Fluoroacetophenone

isopropyl alcohol
67-63-0,8013-70-5

isopropyl alcohol

acetone
67-64-1

acetone

(1S)-1-(2-fluorophenyl)ethanol
171032-87-4

(1S)-1-(2-fluorophenyl)ethanol

(R)-1-(2-fluorophenyl)ethanol
162427-79-4

(R)-1-(2-fluorophenyl)ethanol

Conditions
Conditions Yield
With C32H31Cl2N4OPRu; potassium isopropoxide; at 30 ℃; for 0.5h; under 750.075 Torr; optical yield given as %ee; enantioselective reaction; Inert atmosphere;
 
With potassium hydroxide; at 82 ℃; for 0.5h; Reagent/catalyst; enantioselective reaction; Catalytic behavior; Inert atmosphere; Schlenk technique;
45 % ee

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    JN 403

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