((4-Trifluoromethyl)phenyl)di-tert-butylphosphine
Product Information
Molecular Formula
C15H22F3P
Molecular Weight
290.30
Description
4-Trifluoromethylphenyl)di-tert-butylphosphine is an intricate biochemical constituent that functions as a catalyst, engendering chemical metamorphoses integral to the biologically active molecular creation.
Synonyms
Di-tert-butyl(4-(trifluoromethyl)phenyl)phosphine; ((4-Trifluoromethyl)phenyl)di-tert-butylphosphine; ditert-butyl-[4-(trifluoromethyl)phenyl]phosphane; Di-tert-butyl[4-(trifluoromethyl)phenyl]phosphane; [4-(Trifluoromethyl)phenyl]di-tert-butylphosphine; Di-tert-butyl (4-(trifluoromethyl)phenyl)phosphine; ((4-TrifluoroMethyl)phenyl)di-tert-butylphosphine,85per cent; Phosphine, bis(1,1-dimethylethyl)[4-(trifluoromethyl)phenyl]-; ((4-Trifluoromethyl)phenyl)di-tert-butylphosphine, technical grade, 85%
IUPAC Name
ditert-butyl-[4-(trifluoromethyl)phenyl]phosphane
SMILES
CC(C)(C)P(C1=CC=C(C=C1)C(F)(F)F)C(C)(C)C
InChI
InChI=1S/C15H22F3P/c1-13(2,3)19(14(4,5)6)12-9-7-11(8-10-12)15(16,17)18/h7-10H,1-6H3
InChI Key
ILWCCADVRXVLTN-UHFFFAOYSA-N
Melting Point
34-39 °C
Flash Point
111.0 °F
Purity
85%
Safety Information
Hazards
H228 - H315 - H319 - H335 - H413
Precautionary Statement
P210 - P273 - P302 + P352 - P305 + P351 + P338
Computed Properties
XLogP3
4.3
Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
3
Rotatable Bond Count
3
Exact Mass
290.14112219 g/mol
Monoisotopic Mass
290.14112219 g/mol
Topological Polar Surface Area
0Ų
Heavy Atom Count
19
Formal Charge
0
Complexity
274
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
0
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
Covalently-Bonded Unit Count
1
Compound Is Canonicalized
Yes
Patents
| Publication Number | Title | Priority Date |
|---|---|---|
| CN-113845478-A | Intermediate, preparation method and application thereof | 2020-12-18 |
| WO-2020152200-A1 | Process for preparation of heteroarylketones | 2019-01-25 |
| CN-105392791-B | The improved method for preparing chloro acyl benzidine and benzidine | 2013-07-23 |
| EP-3024836-A1 | Improved process for preparing chlorinated biphenylanilides and biphenylanilines | 2013-07-23 |
| EP-3024836-B1 | Improved method for the preparation of chlorinated biphenylanilides and biphenylanilines | 2013-07-23 |
| EP-3418284-A1 | Improved method for the preparation of chlorinated biphenylanilides and biphenylanilines | 2013-07-23 |
| TW-201546031-A | Improved method for preparing chlorinated biphenylamine benzene and biphenylaniline | 2013-07-23 |
| US-2016280635-A1 | Improved process for preparing chlorinated biphenylanilides and biphenylanilines | 2013-07-23 |
| US-9868694-B2 | Process for preparing chlorinated biphenylanilides and biphenylanilines | 2013-07-23 |
| WO-2015011032-A1 | Improved process for preparing chlorinated biphenylanilides and biphenylanilines | 2013-07-23 |
