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1,3,5-Trichlorobenzene is an organochlorine compound. It is one of the three isomers of trichlorobenzene. Being more symmetrical than the other isomers, it exists as colourless crystals whereas the other isomers are liquids at room temperature. It is not formed upon chlorination of benzene. Instead it is prepared by the Sandmeyer reaction from ...
Infobox references. 1,3,5-Trimethyl-1,3,5-triazinane is an organic compound with the formula (CH 3 NCH 2) 3. It is a colorless liquid that is soluble in many organic solvents. Structurally, it is one of several related hexahydro-1,3,5-triazines, which typically result from the condensation reaction of amines and formaldehyde.
Infobox references. 2,4,5-Trichlorophenoxyacetic acid (also known as 2,4,5-T), a synthetic auxin, is a chlorophenoxy acetic acid herbicide used to defoliate broad-leafed plants. It was developed in the late 1940s, synthesized by reaction of 2,4,5-Trichlorophenol and chloroacetic acid. It was widely used in the agricultural industry until being ...
Hexahydro-1,3,5-triazine. In chemistry, hexahydro-1,3,5-triazine is a class of heterocyclic compounds with the formula (CH 2 NR) 3. Known as aldehyde ammonias, these compounds characteristically crystallize with water. They are reduced derivatives of 1,3,5- triazine, which have the formula (CHN) 3, a family of aromatic heterocycles.
1,3,5-tris (4-formylphenyl)benzene (TFPB) 1,3,5-Tribromobenzene is a precursor to C 3 -symmetric molecules. It undergoes a Suzuki reaction with three equivalents of 4-formylphenylboronic acid to form 1,3,5-tris (4-formylphenyl)benzene (TFPB), a monomer for covalent organic frameworks. [4]
Infobox references. 2,4,6-Tris (trinitromethyl)-1,3,5-triazine is a chemical compound that is a derivative of triazine first prepared in 1995. [1] It is synthesized by destructive nitration of 2,4,6-tricarboxyl-1,3,5-triazine. It is noteworthy for having more nitro groups than it does carbon atoms, thus potentially being useful as an oxygen ...
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