10487-10-2

Basic information

• Product Name: 2-Pentanone, 5,5,5-trifluoro-4-hydroxy-4-(trifluoromethyl)-
• Synonyms: 2-Pentanone, 5,5,5-trifluoro-4-hydroxy-4-(trifluoromethyl)-;1,1,1-Trifluoro-2-hydroxy-2-(trifluoromethyl)pentan-4-one;5,5,5-Trifluoro-4-hydroxy-4-(trifluoromethyl)-2-pentanone;5,5,5-trifluoro-4-hydroxy-4-(trifluoromethyl)pentan-2-one;1,1,1-Trifluoro-2-trifluoromethyl-2-hydroxy pentan-4-one
• CAS NO: 10487-10-2
• Molecular Formula: C₆H₆F₆O₂
• Molecular Weight: 224.1010592
• Mol File: 10487-10-2.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 195℃
• Flash Point: 71℃
• Appearance: /
• Density: 1.445
• Vapor Pressure: 0.043mmHg at 25°C
• Refractive Index: 1.3430
• CAS DataBase Reference: 2-Pentanone, 5,5,5-trifluoro-4-hydroxy-4-(trifluoromethyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Pentanone, 5,5,5-trifluoro-4-hydroxy-4-(trifluoromethyl)-(10487-10-2)
• EPA Substance Registry System: 2-Pentanone, 5,5,5-trifluoro-4-hydroxy-4-(trifluoromethyl)-(10487-10-2)

Safety Data

• Hazardous Substances Data: 10487-10-2(Hazardous Substances Data)

Usage

General Description

2-Pentanone, 5,5,5-trifluoro-4-hydroxy-4-(trifluoromethyl)- is a chemical compound with the molecular formula C6H7F6O. It is a trifluorinated derivative of 2-pentanone and is also known as trifluoroacetoin. 2-Pentanone, 5,5,5-trifluoro-4-hydroxy-4-(trifluoromethyl)- is commonly used as a solvent in organic synthesis and as a reagent in pharmaceutical and chemical research. Its unique structure and properties make it useful in various applications, such as in the production of flavors and fragrances, as well as in the synthesis of pharmaceutical drugs and agrochemicals. Additionally, 2-Pentanone, 5,5,5-trifluoro-4-hydroxy-4-(trifluoromethyl)- has potential applications in the development of new materials and as a building block for the synthesis of other organofluorine compounds.

InChI:InChI=1/C5H2ClFN2O2/c6-5-4(9(10)11)1-3(7)2-8-5/h1-2H

Upstream product

• 684-16-2 Hexafluoroacetone 
• 67-64-1 acetone 

Downstream Products

• 34844-48-9 1,1,1-trifluoro-2-(trifluoromethyl)pentane-2,4-diol 
• 1108201-91-7 TiCl(OCH(CH₃)2)((CF₃)2C(O)CH₂COCH₃)2 
• 86350-38-1 Cu((CF₃)2COCH₂C(CH₃)N(C₆H₁₁))2 
• 86350-39-2 Cu((CF₃)2COCH₂C(CH₃)N(CH₂C₆H₅))2 
• 86350-42-7 Cu((CF₃)2COCH₂C(CH₃)N(C₆H₉(CH₃)(CH(CH₃)2)))2 
• 86350-41-6 Cu((CF₃)2COCH₂C(CH₃)N(CH(CH₃)(C₆H₅)))2 

Relevant articles and documents

Aluminum, indium, and mixed yttrium-lithium complexes supported by a chiral binap-based fluorinated dialkoxide: Structural features and heteroselective ROP of lactide

The new chiral Binap-based fluorinated dialcohol proteo-ligand {ONNO}H2 has been prepared under its enantiomerically pure and racemic forms following reaction of (R)- or (rac)-1,1′-binaphthyl-2,2′-diamine with 5,5,5-trifluoro-4-hydroxy-4-(trifluoromethyl)pentan-2-one. The racemic proteo-ligand reacts with the trivalent metallic precursors AlEt2Cl and In(CH2SiMe3)3 to yield the complexes (rac)-{ONNO}AlCl (1) and (rac)-{ONNO}In(CH2SiMe3) (2), while the reaction of (R)-{ONNO}H2 with a 1:1 mixture of Y(N(SiMe3)2)3 and LiN(SiMe3)2 gives the enantiomerically pure heterobimetallic [((R)-{ONNO})2Y·Li] (3). Complex 3 acts as a single-component initiator for the near-perfect heteroselective ring-opening polymerization (ROP) of racemic lactide, yielding polymers with Pr up to 0.99 under mild conditions. It also produces syndiotactic-enriched polylactide (Pr = 0.80) by ROP of meso lactide.

Convenient synthesis of mono- and di-β-hydroxy-β-bis(trifluoromethyl)-(di)imines from β-hydroxy-β-bis(trifluoromethyl)-ketones and (di)amines

A series of novel β-hydroxy-β-bis(trifluoromethyl)-imines (2a-j) and di(β-hydroxy-β-bis(trifluoromethyl))-diimines (3a-f) were prepared in moderate to good yields via a simple two-step approach: first, β-hydroxy-β-bis(trifluoromethyl)-ketones (1a-c) were

Fluorinated alkoxy-imino catalyst components

This invention relates to fluorinated alkoxy-imino metallic complexes and their use in catalyst systems for the polymerisation or oligomerisation of ethylene and alpha-olefins.