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Merck
CN

107565

1,1,1,3,3,3-Hexafluoro-2-phenyl-2-propanol

97%

Synonym(s):

α,α-Bis(trifluoromethyl)benzyl alcohol

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About This Item

Linear Formula:
C6H5C(CF3)2OH
CAS Number:
718-64-9
Molecular Weight:
244.13
NACRES:
NA.22
PubChem Substance ID:
24846770
UNSPSC Code:
12352100
EC Number:
211-943-4
MDL number:
MFCD00040983
Assay:
97%

Key Documents

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InChI key

IZPIZCAYJQCTNG-UHFFFAOYSA-N

InChI

1S/C9H6F6O/c10-8(11,12)7(16,9(13,14)15)6-4-2-1-3-5-6/h1-5,16H

SMILES string

OC(c1ccccc1)(C(F)(F)F)C(F)(F)F

refractive index

n20/D 1.415 (lit.)

bp

160 °C (lit.)

density

1.45 g/mL at 25 °C (lit.)

functional group

fluoro, hydroxyl, phenyl

Quality Level

100

assay

97%

Related Categories

Biochem/physiol Actions

1,1,1,3,3,3-Hexafluoro-2-phenyl-2-propanol is an effective solvent for Cu(0)-mediated single electron transfer-living radical polymerization of methyl methacrylate and polymerization of styrene.

pictograms

FlameExclamation mark
GHS02,GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

3 - Flammable liquids

wgk

WGK 3

flash_point_f

140.0 °F - closed cup

flash_point_c

60 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
MKDB0670
MKCV3939
MKBF5878V
09198MJ
17726DE

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Single electron transfer-living radical polymerization of methyl methacrylate in fluoroalcohol: Dual control over molecular weight and tacticity.
Wang W, et al.
Journal of Polymer Science Part A: Polymer Chemistry, 47(22), 6316-6327 (2009)
Cyclic alkoxyamine-initiator tethered by azide/alkyne-?click?-chemistry enabling ring-expansion vinyl polymerization providing macrocyclic polymers.
Narumi A, et al.
Journal of Polymer Science Part A: Polymer Chemistry, 48(15), 3402-3416 (2010)
Marcus Maschke et al.
ChemMedChem, 9(6), 1188-1194 (2014-05-20)
We report the synthesis of trifluoromethylated metallocenes (M=Fe, Ru) and related metal-free compounds for comparison of their biological properties with the aim to establish structure-activity relationships toward the anti-proliferative activity of this compound class. All new compounds were comprehensively characterized

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