937399-81-0

Basic information

• Product Name: (R)-(+)-1-(3,4,5-trifluorophenyl)ethanol
• Synonyms: (R)-(+)-1-(3,4,5-trifluorophenyl)ethanol
• CAS NO: 937399-81-0
• Molecular Weight: 176.138
• Mol File: 937399-81-0.mol

Chemical Properties

• CAS DataBase Reference: (R)-(+)-1-(3,4,5-trifluorophenyl)ethanol(CAS DataBase Reference)
• NIST Chemistry Reference: (R)-(+)-1-(3,4,5-trifluorophenyl)ethanol(937399-81-0)
• EPA Substance Registry System: (R)-(+)-1-(3,4,5-trifluorophenyl)ethanol(937399-81-0)

Safety Data

• Hazardous Substances Data: 937399-81-0(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
(R)-(+)-1-(3,4,5-trifluorophenyl)ethanol is used as a chiral building block for the synthesis of various pharmaceuticals. Its unique chiral properties allow for the creation of drugs with specific therapeutic effects, enhancing the efficacy and selectivity of medications.
Used in Agrochemical Industry:
In the agrochemical sector, (R)-(+)-1-(3,4,5-trifluorophenyl)ethanol is utilized as a key component in the development of new agrochemicals. Its chiral nature enables the production of targeted and effective compounds for pest control and crop protection.
Used in Organic Synthesis:
(R)-(+)-1-(3,4,5-trifluorophenyl)ethanol is employed as a versatile building block in organic synthesis. Its reactivity and chirality make it a valuable component in the creation of complex organic molecules for various applications.
Used in Development of New Materials:
(R)-(+)-1-(3,4,5-trifluorophenyl)ethanol has potential applications in the development of new materials, leveraging its unique properties to create innovative and improved materials for a range of uses.
Used in Catalytic Processes:
(R)-(+)-1-(3,4,5-trifluorophenyl)ethanol is also utilized in catalytic processes, where its chiral nature can enhance the selectivity and efficiency of chemical reactions, leading to more sustainable and cost-effective production methods.
Overall, (R)-(+)-1-(3,4,5-trifluorophenyl)ethanol is a valuable compound in the chemical and pharmaceutical industries, with a wide range of applications due to its chiral nature and versatile reactivity.

Upstream product

• 220141-73-1 1-(3,4,5-trifluorophenyl)ethanone 
• 111-42-2 2,2'-iminobis[ethanol] 

Downstream Products

• 937399-82-1 5-((S)-1-azidoethyl)-1,2,3-trifluorobenzene 

Relevant articles and documents

Origin of enantioselectivity in the Ru(arene)(amino alcohol)-catalyzed transfer hydrogenation of ketones

The origin of the enantioselectivity in the ruthenium-catalyzed transfer hydrogenation has been studied by means of experiment and density functional theory calculations. The results clearly show that electrostatic effects are of importance, not only in the T-shaped arene-aryl interaction in the favored transition state but also between the aryl of the substrate and the amine ligand in the disfavored TS. In addition, the electrostatic interaction between the alkyl substituent of the substrate and the catalyst is of importance to the enantioselectivity. The major cause of enantioselection is found to be of nonelectrostatic origin. This inherent property of the catalytic system is discussed in terms of dispersion forces and solvent effects. Finally, a minor but well-characterized steric effect was identified. The success of this class of catalysts in the reduction of alkyl aryl ketones is based on the fact that all factors work in the same direction.

HETEROCYCLIC TYPE CINNAMIDE DERIVATIVE

Disclosed is a compound represented by the formula (I) below or a pharmacologically acceptable salt thereof. Also disclosed is a use of the compound or salt as a pharmaceutical product. (In the formula, Ar1 represents a triazolyl group or the l

Morpholine type cinnamide compound

The present invention relates to a compound represented by the formula (I): or a pharmacologically acceptable salt thereof, wherein R1, R2, R3, and R4 are the same or different and each represent a hydrogen atom or a C1-6 alkyl group; X1 represents a C1-6 alkylene group that may be substituted; Xa represents a methoxy group or a fluorine atom; Xb represents an oxygen atom or a methylene group, provided that Xb is only an oxygen atom when Xa is a methoxy group; and Ar1 represents an aryl group, pyridinyl group, aryloxy group, or pyridinyloxy group that may have a substituent such as a halogen atom; and to use of the compound or salt as a pharmaceutical agent.