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
Canonical 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
The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

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