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121250-04-2

121250-04-2

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121250-04-2 Usage

Uses

(R)-Trifluorolactic Acid is a stereoisomer of (S)-Trifluorolactic Acid (T790500) which can be used as a chiral derivatizing agent for alcohols.

Check Digit Verification of cas no

The CAS Registry Mumber 121250-04-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,1,2,5 and 0 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 121250-04:
(8*1)+(7*2)+(6*1)+(5*2)+(4*5)+(3*0)+(2*0)+(1*4)=62
62 % 10 = 2
So 121250-04-2 is a valid CAS Registry Number.
InChI:InChI=1/C3H3F3O3/c4-3(5,6)1(7)2(8)9/h1,7H,(H,8,9)/t1-/m1/s1

121250-04-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (R)-3,3,3-TRIFLUORO-2-HYDROXYPROPIONIC ACID

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:121250-04-2 SDS

121250-04-2Downstream Products

121250-04-2Relevant articles and documents

Self-disproportionation of enantiomers of isopropyl 3,3,3-(trifluoro)lactate via sublimation: Sublimation rates vs. enantiomeric composition

Yasumoto, Manabu,Ueki, Hisanori,Ono, Taizo,Katagiri, Toshimasa,Soloshonok, Vadim A.

, p. 535 - 539 (2010)

The presented results convincingly demonstrate that self-disproportionation of enantiomers via sublimation is substantially more complex phenomenon then was previously believed. We demonstrate that the racemic form of isopropyl 3,3,3-trifluoro-2-hydroxypr

Enantioselective synthesis of 1,1,1-trifluoroalkan-2-ols by ruthenium- catalyzed hydrogenation

Kuroki, Yoshichika,Asada, Daisuke,Sakamaki, Yuko,Iseki, Katsuhiko

, p. 4603 - 4607 (2007/10/03)

The highly enantioselective synthesis of 1,1,1-trifluoroalkan-2-ols has been achieved by hydrogenating 1,1,1-trifluoroalkan-2-one enol acetates in the presence of chiral ruthenium catalysts. An enol acetate, 2-acetoxy-3,3,3- trifluoro-1-(phenylthio)propen

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