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108211-36-5

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108211-36-5 Usage

General Description

(R)-4,4,4-Trifluoro-3-hydroxybutyric acid is a chemical compound possessing specific structural properties. These include a trifluoro functional group, which consists of three fluorine atoms, attached to the fourth carbon (4,4,4). Additionally, it has a hydroxy (or alcohol) functional group on the third carbon and a carboxylic acid group on one end. The (R) in its name refers to the configuration of the molecule, indicating it is the right-handed (rectus) enantiomer of the compound. (R)-4,4,4-TRIFLUORO-3-HYDROXYBUTYRIC ACID may be used in various applications in the field of synthetic organic chemistry. Its properties may also lend it unique reactivity, making it potentially useful in creating pharmaceuticals, agrochemicals, polymers and materials.

Check Digit Verification of cas no

The CAS Registry Mumber 108211-36-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,8,2,1 and 1 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 108211-36:
(8*1)+(7*0)+(6*8)+(5*2)+(4*1)+(3*1)+(2*3)+(1*6)=85
85 % 10 = 5
So 108211-36-5 is a valid CAS Registry Number.
InChI:InChI=1/C4H5F3O3/c5-4(6,7)2(8)1-3(9)10/h2,8H,1H2,(H,9,10)/t2-/m0/s1

108211-36-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name (R)-4,4,4-TRIFLUORO-3-HYDROXYBUTYRIC ACID

1.2 Other means of identification

Product number -
Other names R-TFHBA

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:108211-36-5 SDS

108211-36-5Relevant articles and documents

Thiophene as a structural element in physiologically active substances. 15. Thiophene analogs of an anxiolytic acting 1,2,4-triazolo[4,3-b]pyridazine

Binder,Noe,Baumann,Wildburger

, p. 243 - 249 (1985)

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Lewis,E.S. et al.

, p. 662 - 668 (1968)

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On the structure of PHB (=Poly[(R)-3-hydroxybutanoic acid]) in phospholipid bilayers: Preparation of trifluoromethyl-labeled oligo[(R)-3-hydroxybutanoic acid] derivatives

Rueping, Magnus,Albert, Matthias,Seebach, Dieter

, p. 2473 - 2486 (2007/10/03)

Oligomers of (R)-3-hydroxybutanoate (OHB) have previously been shown to transport cations through lipid bilayers. The ion-transport activity has been attributed to the formation of hydrophobic aggregates or pores, which have been identified by fluorescenc

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