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METHYLPHOSPHINE

Methylphosphine

Chemical compound

Methylphosphine is the simplest organophosphine compound with the formula CH3PH2, often written MePH2. It is a malodorous gas that condenses to a colorless

Methylphosphine

Organophosphine

Class of chemical compounds

by alkylation of phosphine. Some simple alkyl derivatives such as methylphosphine (CH3PH2) can be prepared by alkylation of phosphine in the presence

Organophosphine

List of gases

Phosphorus(III) bromide difluoride PBrF2 −16.1 −133.8 149 15597-40-7 Methylphosphine CH3PH2 −16 48 593-54-4 Fluorine perchlorate FOClO3 −16 −167.3 118.5

List of gases

List_of_gases

N-Butyllithium

Chemical compound

methyl sulfides (H−CH2SR), thioacetals (H−CH(SR)2, e.g. dithiane), methylphosphines (H−CH2PR2), furans, thiophenes and ferrocene (Fe(H−C5H4)(C5H5)). In

N-Butyllithium

Proton affinity

Property of ions and molecules

ether 838 Dimethyl sulfide 839 Iron pentacarbonyl 845 Ammonia 854 Methylphosphine 854 Hydrazine 856 Diethyl sulfide 858 1,6-Dicarba-closo-hexaborane(6)

Proton affinity

Proton_affinity

Stench compound

mostly of dicacodyl (((CH3)2As)2) and cacodyl oxide (((CH3)2As)2O). The methylphosphines ((CH3)PH2, (CH3)2PH, and (CH3)3P have a garlic-metallic odors. In contrast

Stench compound

Stench_compound

Metallacycle

Cyclic compound with at least one metal atom in its ring structure

groups, an early example being the internal oxidative addition of methylphosphine ligands. Metallacycle formation interferes with intermolecular C-H

Metallacycle

Diphosphenes

Organophosphorus compound with a phosphorus–phosphorus double bond

obtained by treating Na2[Fe(CO)4] with dichlorobis(trimethylsilyl)methylphosphine. The related complex [ArP=PAr]Fe(CO)4 (Ar=2,4,6-tri-tert-butylphenyl)

Diphosphenes