121170-45-4 Usage
Description
(R)-(+)-1,1,1-TRIFLUOROOCTAN-2-OL 97, with the molecular formula C8H16F3O, is a clear, colorless liquid characterized by a strong, pungent odor. This chemical compound is recognized for its high purity level of 97% and is utilized in various applications across different industries due to its unique properties.
Uses
Used in Organic Synthesis:
(R)-(+)-1,1,1-TRIFLUOROOCTAN-2-OL 97 is used as a key intermediate in organic synthesis for the production of various chemical compounds. Its unique structure and reactivity make it a valuable component in creating new molecules with specific properties.
Used in Pharmaceutical Production:
In the pharmaceutical industry, (R)-(+)-1,1,1-TRIFLUOROOCTAN-2-OL 97 serves as an intermediate in the synthesis of drugs. Its presence in the manufacturing process contributes to the development of medications with targeted therapeutic effects.
Used in Agrochemicals:
(R)-(+)-1,1,1-TRIFLUOROOCTAN-2-OL 97 is also utilized as an intermediate in the production of agrochemicals, which are essential for enhancing crop protection and improving agricultural yields.
Used as a Solvent:
(R)-(+)-1 1 1-TRIFLUOROOCTAN-2-OL 97 is employed as a solvent in various chemical reactions due to its ability to dissolve a wide range of substances. Its solvent properties facilitate efficient reaction conditions and improved product yields.
Used as a Reagent:
(R)-(+)-1,1,1-TRIFLUOROOCTAN-2-OL 97 functions as a reagent in chemical reactions, participating directly in the transformation of other compounds. Its reactivity allows for the synthesis of new products with desired characteristics.
Used in Environmental Remediation:
With potential applications in environmental remediation, (R)-(+)-1,1,1-TRIFLUOROOCTAN-2-OL 97 can be utilized to address pollution and contamination issues. Its properties may contribute to the development of solutions for cleaning up environmental hazards.
It is crucial to handle (R)-(+)-1,1,1-TRIFLUOROOCTAN-2-OL 97 with care, as its improper use can lead to hazardous consequences. The high purity and versatile applications of this compound make it an essential component in various industrial processes.
Check Digit Verification of cas no
The CAS Registry Mumber 121170-45-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,1,1,7 and 0 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 121170-45:
(8*1)+(7*2)+(6*1)+(5*1)+(4*7)+(3*0)+(2*4)+(1*5)=74
74 % 10 = 4
So 121170-45-4 is a valid CAS Registry Number.
InChI:InChI=1/C8H15F3O/c1-2-3-4-5-6-7(12)8(9,10)11/h7,12H,2-6H2,1H3/t7-/m1/s1
121170-45-4Relevant articles and documents
Syntheses of (R)- and (S)-enantiomeric 1,1,1-trifluoromethyl-2-alkanols with high enantiomeric purity controlled through derivatization with l-menthyl phthalate
Mikhailenko, Vadim,Yedamenko, Daria,Vlasenko, Ganna,Krivoshey, Alexander,Vashchenko, Valerii
, p. 5956 - 5959 (2015/11/02)
Readily available l-menthyl phthalate has been shown to be an effective derivatizing agent for determination of the enantiomeric purity of alkyl- and aryl-substituted 1,1,1-trifluoromethyl-2-alkanols using HPLC and GC. It has been shown that a previously described protocol for one-step enzymatic kinetic resolution results in the formation of the desired 1,1,1-trifluoromethyl-2-alkanols with 96-98% ee. Enrichment of the (R)-isomer of trifluoromethyl alkanols by repetition of the enzymatic hydrolysis procedure was found to increase the ee up to 99.9%. Furthermore, excessive conversion of the corresponding esters during enzymatic hydrolysis allowed enantiomerically pure (S)-1,1,1-trifluoromethyl-2-alkanols to be obtained.
New chiral dopant possessing high twisting power
Pozhidaev,Torgova,Molkin,Minchenko,Vashchenko,Krivoshey,Strigazzi
, p. 300 - 308 (2011/08/02)
We have synthesized and investigated a new chiral dopant. It belongs to the derivatives of p-terphenyldicarboxylic acid and has twisting power in the smectic C* mixture much higher than any chiral compound of this series known before. The ferroelectric liquid crystal mixtures on the base of achiral SmC matrix and the new chiral dopant have been elaborated and there optical and electro-optical properties were investigated. Copyright Taylor & Francis Group, LLC.
Enantioselective Rhodium(I)-Catalyzed Hydrogenation of Trifluoromethyl Ketones
Kuroki, Yoshichika,Sakamaki, Yuko,Iseki, Katsuhiko
, p. 457 - 459 (2007/10/03)
(Matrix Presented) The asymmetric hydrogenation of trifluoromethyl ketones to yield chiral α-trifluoromethyl alcohols with enantiomeric excesses up to 98% was achieved in the presence of chiral rhodium-(amidephosphine-phosphinite) complexes.
