1,1,1,3,3,3-Hexafluoro-2-methyl-2-propanol - CAS 1515-14-6
Catalog: |
BB010675 |
Product Name: |
1,1,1,3,3,3-Hexafluoro-2-methyl-2-propanol |
CAS: |
1515-14-6 |
Synonyms: |
1,1,1,3,3,3-hexafluoro-2-methylpropan-2-ol |
IUPAC Name: | 1,1,1,3,3,3-hexafluoro-2-methylpropan-2-ol |
Description: | 1,1,1,3,3,3-Hexafluoro-2-methyl-2-propanol (CAS# 1515-14-6) is used as an activator for the chemical fixation of carbon dioxide onto epoxides. Also used as a reagent in the synthesis of highly substituted furfuryl alcohols and amines. |
Molecular Weight: | 182.06 |
Molecular Formula: | C4H4F6O |
Canonical SMILES: | CC(C(F)(F)F)(C(F)(F)F)O |
InChI: | InChI=1S/C4H4F6O/c1-2(11,3(5,6)7)4(8,9)10/h11H,1H3 |
InChI Key: | FQDXJYBXPOMIBX-UHFFFAOYSA-N |
Boiling Point: | 93.5 ℃ at 760 mmHg |
Density: | 60 |
Appearance: | Clear colorless liquid |
MDL: | MFCD00039259 |
LogP: | 1.86200 |
GHS Hazard Statement: | H302 (89.36%): Harmful if swallowed [Warning Acute toxicity, oral] |
Precautionary Statement: | P261, P264, P270, P271, P280, P301+P312, P302+P352, P304+P312, P304+P340, P305+P351+P338, P312, P321, P322, P330, P332+P313, P337+P313, P362, P363, P403+P233, P405, and P501 |
Signal Word: | Warning |
Publication Number | Title | Priority Date |
CN-112794787-A | Method for continuously preparing 3,3, 3-trifluoro-2- (trifluoromethyl) -1-propylene in gas phase | 20210408 |
CN-112794787-B | Method for continuously preparing 3,3, 3-trifluoro-2- (trifluoromethyl) -1-propylene in gas phase | 20210408 |
CN-112500270-A | Method for synthesizing alpha, alpha-difluoroketone compound | 20201203 |
JP-2020140217-A | Polarizing plate protective film and polarizing plate | 20200610 |
WO-2021172380-A1 | Method for analyzing nucleic acid drugs | 20200225 |
PMID | Publication Date | Title | Journal |
22904761 | 20120801 | Bis(1,2-dimethoxyethane)-1κ(2)O,O';3κ(2)O,O'-tetra-kis-(μ-1,1,1,3,3,3-hexa-fluoro-2-methyl-propan-2-olato)-1:2κ(4)O:O;2:3κ(4)O:O-1,3-dilithium-2-magnesium | Acta crystallographica. Section E, Structure reports online |
21968346 | 20111111 | Fluoroalcohols as novel buffer components for basic buffer solutions for liquid chromatography electrospray ionization mass spectrometry: retention mechanisms | Journal of chromatography. A |
21922097 | 20111107 | Two fluoroalcohols as components of basic buffers for liquid chromatography electrospray ionization mass spectrometric determination of antibiotic residues | The Analyst |
17165793 | 20061220 | Dipyrrolyl precursors to bisalkoxide molybdenum olefin metathesis catalysts | Journal of the American Chemical Society |
Complexity: | 130 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 182.01663372 |
Formal Charge: | 0 |
Heavy Atom Count: | 11 |
Hydrogen Bond Acceptor Count: | 7 |
Hydrogen Bond Donor Count: | 1 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 182.01663372 |
Rotatable Bond Count: | 0 |
Topological Polar Surface Area: | 20.2 Å2 |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 0 |
XLogP3: | 1.8 |
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