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General chemical structure of the organophosphate functional group. In organic chemistry, organophosphates (also known as phosphate esters, or OPEs) are a class of organophosphorus compounds with the general structure O=P(OR) 3, a central phosphate molecule with alkyl or aromatic substituents. [1] They can be considered as esters of phosphoric ...
In organic chemistry, phosphate or orthophosphate is an organophosphate, an ester of orthophosphoric acid of the form PO 4 RR′R″ where one or more hydrogen atoms are replaced by organic groups. An example is trimethyl phosphate, (CH 3) 3 PO 4. The term also refers to the trivalent functional group OP(O-) 3 in such esters.
Terbufos, also known as S-((tert-butylthio)methyl) O,O-diethyl phosphorodithioate, [17] is a compound classified as an organophosphate.Terbufos consists of a central phosphorus atom, surrounded by four different groups.
Organophosphorus chemistry is the scientific study of the synthesis and properties of organophosphorus compounds, which are organic compounds containing phosphorus. [1] They are used primarily in pest control as an alternative to chlorinated hydrocarbons that persist in the environment.
Organophosphates are esters and ester derivatives of phosphoric acid. Ester derivatives include: Ester halides (Category:Organophosphorohalidates)
Alkyl phosphates belong to a group of organic compounds called organophosphates. They are esters of phosphoric acid H 3 PO 4 and corresponding alcohol. For example, the formula of methyl phosphate is CH 3-H 2 PO 4, dimethyl phosphate – (CH 3) 2 HPO 4 and trimethyl phosphate – (CH 3) 3 PO 4. Alkyl phosphates are widely distributed in nature ...
Malathion is an organophosphate insecticide which acts as an acetylcholinesterase inhibitor. In the USSR , it was known as carbophos , in New Zealand and Australia as maldison and in South Africa as mercaptothion .
Most processes begin with phosphorous acid (aka phosphonic acid, H 3 PO 3), exploiting its reactive P−H bond. [1] [3]Phosphonic acid can be alkylated via the Kabachnik–Fields reaction or Pudovik reaction to give aminophosphonate, which are useful as chelating agents.