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[3] [4] [5] The notions behind orthomolecular medicine are not supported by sound medical evidence, and the therapy is not effective for chronic disease prevention; [6] [7] even the validity of calling the orthomolecular approach a form of medicine has been questioned since the 1970s. [8]
o-Toluidine (ortho-toluidine) is an organic compound with the chemical formula CH 3 C 6 H 4 NH 2. It is the most important of the three isomeric toluidines. It is a colorless liquid although commercial samples are often yellowish. It is a precursor to the herbicides metolachlor and acetochlor. [2]
Triethyl orthoformate is an organic compound with the formula HC(OC 2 H 5) 3. This colorless volatile liquid, the ortho ester of formic acid , is commercially available. The industrial synthesis is from hydrogen cyanide and ethanol.
Structures of the three isomers of tolyl group. In organic chemistry, tolyl groups are functional groups related to toluene. [1] They have the general formula CH 3 C 6 H 4 −R, the change of the relative position of the methyl and the R substituent on the aromatic ring can generate three possible structural isomers 1,2 (ortho), 1,3 (meta), and 1,4 (para).
Lead(IV) hydroxide, Pb(OH) 4, also called ortho-plumbic acid, is the notional conjugate acid of the ortho-plumbate(IV) ion, PbO 4− 4, found in compounds such as calcium orthoplumbate, Ca 2 PbO 4. [ citation needed ] Like its tin analog Sn(OH) 4 , Pb(OH) 4 has not been isolated.
Orthocarbonic acid, carbon hydroxide, methanetetrol is the name given to a hypothetical compound with the chemical formula H 4 CO 4 or C(OH) 4. Its molecular structure consists of a single carbon atom bonded to four hydroxyl groups.
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[2] [3] Orthomolecular psychiatry's goal of weaning patients from conventional neuroleptic drugs [4] follows "Pfeiffer's Law", "For every drug that benefits a patient, there is a natural substance that can achieve the same effect". [5] In 1968, Linus Pauling first used the term orthomolecular. [6] [7]
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