| Identification | Back Directory | [Name]
2-(DI-T-BUTYLPHOSPHINO)-2'-METHYLBIPHENYL | [CAS]
255837-19-5 | [Synonyms]
tBuMePhos
98% tBuMePhos
tBuMePhos 97%
t-Butyl MePhos
2-(DI-T-BUTYLPHOSPHINO)-2'-METHYLBIPHENYL
2-Di-t-butylphosphino-2'-methylbiphenyl,99%
2-(DI-TERT-BUTYLPHOSPHINO)-2'-METHYLBIPHENYL
2-(Di-tert-butylphosphiNA)-2'-Methylbiphenyl
Di-tert-butyl(2'-Methylbiphenyl-2-yl)phosphine
2-Di-t-butylphosphino-2'-methyl)-1,1'-biphenyl
2-(Di-tert-butylphosphino)-2'-methylbiphenyl ,99%
2-(Di-tert-butylphosphino)-2'-methyl- biphenyl, 98+%
Di-tert-butyl(2'-Methyl-[1,1'-biphenyl]-2-yl)phosphine
2-Di-t-butylphosphino-2'-Methylbiphenyl,98% tBuMePhos
2-(Di-t-butylphosphino)-2'-Methylbiphenyl, 99% (tBuMePhos)
2-Di-t-butylphosphino-2'-methyl)-1,1'-biphenyl, 99% t-BuMePhos
PHOSPHINE, BIS(1,1-DIMETHYLETHYL)(2''-METHYL[1,1''-BIPHENYL]-2-YL)- | [EINECS(EC#)]
607-748-2 | [Molecular Formula]
C21H29P | [MDL Number]
MFCD03453047 | [MOL File]
255837-19-5.mol | [Molecular Weight]
312.43 |
| Chemical Properties | Back Directory | [Appearance]
White crystalline powder | [Melting point ]
91-93 °C
| [Boiling point ]
408.0±24.0 °C(Predicted) | [storage temp. ]
Inert atmosphere,Room Temperature | [form ]
Crystalline Powder | [color ]
White | [Sensitive ]
Air Sensitive | [InChI]
InChI=1S/C21H29P/c1-16-12-8-9-13-17(16)18-14-10-11-15-19(18)22(20(2,3)4)21(5,6)7/h8-15H,1-7H3 | [InChIKey]
UJONYAVMBYXBJQ-UHFFFAOYSA-N | [SMILES]
P(C(C)(C)C)(C(C)(C)C)C1=CC=CC=C1C1=CC=CC=C1C |
| Hazard Information | Back Directory | [Chemical Properties]
White crystalline powder | [Uses]
suzuki reaction | [Description]
2-(Di-t-butylphosphino)-2'-methylbiphenyl is a phosphine that has two functional groups, amide and aromatic hydrocarbon. The geometric isomers of this molecule are cis and trans. It can be used to diagnose reactions in a reaction vessel with mammalian cells. It also reacts with pyrazoles, triazoles and other molecules to form isomers at the 2 position of the biphenyl ring. | [Application]
2-(Di-t-butylphosphino)-2'-methylbiphenyl has been shown to have cancer chemotherapeutic potential, as it inhibits the growth of cancer cells by binding to DNA and inhibiting its transcription. This compound also induces apoptosis in some cancer cells. |
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