225920-05-8

  • Product Name:(S)-1-[3,5-Bis(trifluoromethyl)phenyl]ethanol
Inquiry

Product Details

Purity:99%

High Quality 225920-05-8 Factory Price, (S)-1-[3,5-Bis(trifluoromethyl)phenyl]ethanol

  • Molecular Formula:C10H8 F6 O
  • Molecular Weight:258.163
  • Vapor Pressure:0.746mmHg at 25°C 
  • Melting Point:53.0 to 57.0 °C 
  • Boiling Point:223.5°Cat760mmHg 
  • PKA:13.99±0.20(Predicted) 
  • Flash Point:86.6°C 
  • PSA:20.23000 
  • Density:1.457g/cm3 
  • LogP:3.77750 

(S)-1-[3,5-Bis(trifluoromethyl)phenyl]ethanol(Cas 225920-05-8) Usage

Chemical Properties

White solid

Uses

Aprepitant intermediate.

InChI:InChI=1/C10H8F6O/c1-5(17)6-2-7(9(11,12)13)4-8(3-6)10(14,15)16/h2-5,17H,1H3/t5-/m0/s1

225920-05-8 Relevant articles

High-efficient production of (S)-1-[3,5-Bis(trifluoromethyl)phenyl]ethanol via whole-cell catalyst in deep-eutectic solvent-containing micro-aerobic medium system

Bi, Shunde,Wang, Pu,Ye, Ning,Zhu, Zhiren

, (2020)

The ratio of substrate to catalyst (S/C)...

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...

Dynamic Kinetic Resolution of Alcohols by Enantioselective Silylation Enabled by Two Orthogonal Transition-Metal Catalysts

Oestreich, Martin,Seliger, Jan

supporting information, p. 247 - 251 (2020/10/29)

A nonenzymatic dynamic kinetic resolutio...

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...

Abiotic reduction of ketones with silanes catalysed by carbonic anhydrase through an enzymatic zinc hydride

Ji, Pengfei,Park, Jeeyoung,Gu, Yang,Clark, Douglas S.,Hartwig, John F.

, p. 312 - 318 (2021/02/26)

Enzymatic reactions through mononuclear ...

225920-05-8 Process route

vinyl acetate
108-05-4,9003-20-7

vinyl acetate

1-(3,5-bis(trifluoromethyl)phenyl)ethan-1-ol
68120-60-5,127852-28-2,368-63-8

1-(3,5-bis(trifluoromethyl)phenyl)ethan-1-ol

(R)-O-acetyl-1-(3,5-bis(trifluoromethyl)phenyl)ethanol
534613-13-3

(R)-O-acetyl-1-(3,5-bis(trifluoromethyl)phenyl)ethanol

(S)-3,5-bis(trifluoromethyl)-1-phenylethanol
225920-05-8

(S)-3,5-bis(trifluoromethyl)-1-phenylethanol

Conditions
Conditions Yield
With novozyme-435; In diethyl ether; at 20 ℃; for 84h; Resolution of racemate; Enzymatic reaction;
44.6%
48.9%
With Novozyme-435 lipase; In tetrahydrofuran; at 20 ℃; for 72h; Resolution of racemate; Enzymatic reaction;
43%
41%
With 2,6-dimethylpyridine; lipase CAL-B; In toluene; at 40 ℃; for 68h;
5.5 g
vinyl acetate
108-05-4,9003-20-7

vinyl acetate

1-(3,5-bis(trifluoromethyl)phenyl)ethan-1-ol
68120-60-5,127852-28-2,368-63-8

1-(3,5-bis(trifluoromethyl)phenyl)ethan-1-ol

(R)-O-acetyl-1-(3,5-bis(trifluoromethyl)phenyl)ethanol
534613-13-3

(R)-O-acetyl-1-(3,5-bis(trifluoromethyl)phenyl)ethanol

(S)-3,5-bis(trifluoromethyl)-1-phenylethanol
225920-05-8

(S)-3,5-bis(trifluoromethyl)-1-phenylethanol

(R)-[3,5-bis(trifluoromethyl)phenyl]ethanol
368-63-8,68120-60-5,127852-28-2

(R)-[3,5-bis(trifluoromethyl)phenyl]ethanol

Conditions
Conditions Yield
With Novozyme-435 lipase; In tetrahydrofuran; at 20 ℃; for 72h; Resolution of racemate; Enzymatic reaction;
40%
89 % ee
Candida antartica lipase B; In various solvent(s); at 40 ℃; for 2h; under 67505.4 Torr;
 

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