(S)-1,1,1-TRIFLUORO-2-PROPANOL

Base Information

Chemical Name:(S)-1,1,1-TRIFLUORO-2-PROPANOL
CAS No.:17556-48-8
Molecular Formula:C₃H₅F₃O
Molecular Weight:114.067
Hs Code.:
Mol file:17556-48-8.mol

Synonyms:(S)-1,1,1-TRIFLUORO-2-PROPANOL;(S)-1,1,1-TRIFLUOROISOPROPANOL;(S)-1,1,1-Trifluoro-2-propanol(75 % solution in MtBE);(S)-1,1,1-TRIFLUOROISOPROPANOL: 50% SOLUTION IN T-BUTYL METHYL ETHER;50% SOLUTION IN T-BUTYL METHYL ETHER;(S)-1,1,1-TRIFLUORO-2-PROPANOL:98+%( 75 % SOLUTION IN MTBE);(S)-(-)-1,1,1-trifluoro-3-propanol;(S)-1,1,1-Trifluoropropanol

Suppliers and Price of (S)-1,1,1-TRIFLUORO-2-PROPANOL

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

American Custom Chemicals Corporation
(S)-1,1,1-TRIFLUORO-2-PROPANOL 95.00%
5G
$ 1042.97

Total 11 raw suppliers

Chemical Property of (S)-1,1,1-TRIFLUORO-2-PROPANOL

Chemical Property:

Melting Point:-52°C
Refractive Index:1.3130
Boiling Point:53-56°C
Flash Point:-25°C
PSA：20.23000
Density:1.2632
LogP:0.92950

Purity/Quality:

97% ^*data from raw suppliers

(S)-1,1,1-TRIFLUORO-2-PROPANOL 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:
Statements: 11-38
Safety Statements: 9-16-29-33

MSDS Files:: SDS file from LookChem

Useful:

General Description (S)-1,1,1-Trifluoro-2-propanol ((S)-TFP) is an enantioselectively produced alcohol derived from the reduction of 1,1,1-trifluoroacetone (TFA). The enzyme OpCRD-A from *Ogataea polymorpha* NBRC 0799 specifically catalyzes the formation of (S)-TFP with high selectivity, while another enzyme, OpCRD-B, favors the (R)-enantiomer. OpCRD-A exhibits high reductase activity toward fluoroketones and other substrates, operates optimally at acidic pH, and does not dehydrogenate (S)-TFP, making it a promising biocatalyst for efficient (S)-TFP synthesis.

Technology Process of (S)-1,1,1-TRIFLUORO-2-PROPANOL

There total 14 articles about (S)-1,1,1-TRIFLUORO-2-PROPANOL which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 100.0%

: 421-50-1
1,1,1-trifluoro-2-propanone

: 374-01-6,17556-48-8,17628-73-8,3539-97-7
(S)-1,1,1-trifluoro-2-propanol

Guidance literature:: With tetrabutylammomium bromide; water; potassium formate; acetic acid; RuCl[(S,S)-2-naphthylSO₂dpen](mesitylene); at 30 ℃; for 21h; Product distribution / selectivity; Inert atmosphere; Autoclave;

Reference yield: 100.0%

: 421-50-1
1,1,1-trifluoro-2-propanone

: 374-01-6,3539-97-7,17556-48-8,17628-73-8
(R)-1,1,1-trifluoropropanol

Guidance literature:: With formic acid; tetrabutylammomium bromide; water; potassium formate; RuCl[(R,R)-3-ClPhSO₂dpen](mesitylene); at 30 ℃; for 21h; Product distribution / selectivity; Inert atmosphere; Autoclave;