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Molecule
ID:10326
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₈H₁₅F₃O
Molecular Mass
184.1993096
Exact Mass
184.10749976
Charge
0
InChI
InChI=1S/C8H15F3O/c1-2-3-4-5-6-7(12)8(9,10)11/h7,12H,2-6H2,1H3/t7-/m0/s1
InChIKey
INAIBHXNHIEDAM-ZETCQYMHSA-N
Canonic Smiles
CCCCCC[C@@H](C(F)(F)F)O
Isomeric Smiles
CCCCCC[C@@H](C(F)(F)F)O
Calculated Properties
JChem
Acid pKa
11.408001
H Acceptors
1
H Donor
1
LogD (pH = 5.5)
3.1538906
LogD (pH = 7.4)
3.1538486
Log P
3.1538913
Molar Refractivity
41.0582
Polarizability
15.4624405
Polar Surface Area
20.23
Rotatable Bonds
6
Lipinski's Rule of Five
true
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Related Proteins
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Molecular Spectra
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Molecule Details
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Bioactivity
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Bioactivity
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PubChem BioAssay
Data Source
Commercial Catalog
Matrix Scientific
007100
Apollo Scientific
PC0646
Sigma Aldrich
532533
Academic Data
PubChem
7000124
Names and Identifiers
Synonyms
(S)-(-)-1,1,1-Trifluorooctan-2-ol (>98% ee)
(1S)-1-(Trifluoromethyl)heptan-1-ol
(2S)-1,1,1-Trifluorooctan-2-ol (>98%ee)
(S)-(-)-1,1,1-三氟-2-辛醇
(S)-(-)-1,1,1-Trifluoro-2-octanol
IUPAC Traditional name
(2S)-1,1,1-trifluorooctan-2-ol
IUPAC name
(2S)-1,1,1-trifluorooctan-2-ol
Registration numbers
MDL Number
MFCD06799352
CAS Number
129443-08-9
PubChem SID
24877892
160973633
PubChem CID
7000124
Molecule Details
Sigma Aldrich
532533
Packaging
1 g in glass bottle
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay
Properties
Safety Information
TSCA Listed
false
Source
MSDS Link
Download link
Source
Download link
Source
Storage Warning
Irritant
Source
German water hazard class
3
Source
Eyeshields, Gloves, half-mask respirator (US), multi-purpose combination respirator cartridge (US)
Source
Physical Property
75-76°C/20mm
Source
170 °C(lit.)
Source
73 °C
Source
163.4 °F
Source
n20/D 1.384(lit.)
Source
1.05 g/mL at 25 °C(lit.)
Source
Product Information
97%
Source
CF3(CH(OH)(CH2)5CH3
Source
Personal Protective Equipment
Boiling Point
Flash Point
Refractive Index
Density
Purity
Linear Formula