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Phosphine (IUPAC name: phosphane) is a colorless, flammable, highly toxic compound with the chemical formula P H 3, classed as a pnictogen hydride.Pure phosphine is odorless, but technical grade samples have a highly unpleasant odor like rotting fish, due to the presence of substituted phosphine and diphosphane (P 2 H 4).
Phosgene is an organic chemical compound with the formula COCl 2. It is a toxic, colorless gas; in low concentrations, its musty odor resembles that of freshly cut hay or grass. [ 7 ] It can be thought of chemically as the double acyl chloride analog of carbonic acid , or structurally as formaldehyde with the hydrogen atoms replaced by chlorine ...
With the formula (HO) 2 P(O)CH 2 NHCH 2 CO 2 H, this derivative of glycine is one of the most widely used herbicides. Bisphosphonates are a class of drugs to treat osteoporosis. The nerve gas agent sarin, containing both C–P and F–P bonds, is a phosphonate. Phosphinates feature two P–C bonds, with the general formula R 2 P(=O)(OR').
Organophosphines are organophosphorus compounds with the formula PR n H 3−n, where R is an organic substituent.These compounds can be classified according to the value of n: primary phosphines (n = 1), secondary phosphines (n = 2), tertiary phosphines (n = 3).
Tributylphosphine is the organophosphorus compound with the chemical formula P(CH 2 CH 2 CH 2 CH 3) 3, often abbreviated as PBu 3. It is a tertiary phosphine. It is an oily liquid at room temperature, with a nauseating odor. It reacts slowly with atmospheric oxygen, and rapidly with other oxidizing agents, to give tributylphosphine oxide.
Instead of HSiCl 3, other perchloropolysilanes, e.g. hexachlorodisilane (Si 2 Cl 6), can also be used. In comparison, using the reaction of the corresponding phosphine oxides with perchloropolysilanes such as Si 2 Cl 6 or Si 3 Cl 8 in benzene or chloroform, phosphines can be prepared in higher yields. R 3 PO + Si 2 Cl 6 → R 3 P + Si 2 OCl 6
Diphosgene is an organic chemical compound with the formula ClCO 2 CCl 3. This colorless liquid is a valuable reagent in the synthesis of organic compounds. Diphosgene is related to phosgene and has comparable toxicity, but is more conveniently handled because it is a liquid, whereas phosgene is a gas.
telomerization of butadiene to 2.7 octadiene -1-ol with Pd(0) TPPTS. [ 7 ] The Rh(I) TPPTS catalyst was later used by D.Morel to synthesize geranylacetone from myrcene and farnesylacetone from beta-farnesene which are intermediates in the synthesis of vitamin E. [ 8 ] This process was industrialized by Rhône-Poulenc in 1988.