DI-T-BUTYLPHOSPHINE OXIDE
Product Information
Molecular Formula
C8H19OP
Molecular Weight
162.21
Description
DI-T-BUTYLPHOSPHINE OXIDE is a highly versatile biomedicine compound that exhibits multifaceted applications across diverse fields. Functioning as a crucial ligand, catalyst, and organic synthesis reducing agent, it assumes a pivotal role in advancing scientific endeavors. Furthermore, this remarkable compound emerges as a promising therapeutic intervention, effectively ameliorating a plethora of ailments, ranging from cancer to inflammation-related disorders. By intricately modulating cellular processes, it unveils its tremendous therapeutic efficacy, thus pioneering breakthroughs in biomedical research.
Synonyms
2-tert-Butylphosphinoyl-2-methyl-propane; DI-T-BUTYLPHOSPHINE OXIDE; DI-TERT-BUTYLPHOSPHINE OXIDE; Di-t-butylphosphineoxide,98%
IUPAC Name
ditert-butyl(oxo)phosphanium
SMILES
CC(C)(C)[P+](=O)C(C)(C)C
InChI
InChI=1S/C8H18OP/c1-7(2,3)10(9)8(4,5)6/h1-6H3/q+1
InChI Key
QQSIRURWBGEHFS-UHFFFAOYSA-N
Melting Point
74-82 °C
Flash Point
Not applicable
Safety Information
Hazards
H228
Precautionary Statement
P210
Computed Properties
XLogP3
0.9
Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
1
Rotatable Bond Count
2
Exact Mass
161.109527191 g/mol
Monoisotopic Mass
161.109527191 g/mol
Topological Polar Surface Area
17.1Ų
Heavy Atom Count
10
Formal Charge
1
Complexity
120
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-114181250-A | Alkenyl phosphine compound and preparation method thereof | 2020-09-15 |
| WO-2021161851-A1 | Method for producing iodine-containing compound, and polymer | 2020-02-14 |
| CN-110330526-A | A kind of green synthesis method of thio phosphinate | 2019-07-26 |
| CN-110330526-B | Green synthesis method of thiophosphite | 2019-07-26 |
| CN-111848680-A | Bidentate phosphine-phosphine oxide ligand and intermediate, preparation method and application thereof | 2019-04-30 |
| CN-111848680-B | Bidentate phosphine-phosphine oxide ligand and intermediate, preparation method and application thereof | 2019-04-30 |
| CN-111808118-A | Phosphorescent material, manufacturing method thereof and OLED device | 2019-04-12 |
| CN-109867694-A | A kind of synthetic method of the 7- alkynyl Benzazole compounds of oxygen guiding | 2019-03-04 |
| WO-2020177347-A1 | Oxygen-guided synthesis method for 7-alkynyl indole compound | 2019-03-04 |
| CN-109867694-B | Synthesis method of oxygen-guided 7-alkynyl indole compound | 2019-03-04 |
Literatures
| PMID | Publication Date | Title | Journal |
|---|---|---|---|
| 19191507 | 2009-03-05 | Palladium(II)-catalyzed conjugate phosphination of electron-deficient acceptors | Organic letters |
