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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 ...
The most common derivative of 1,3,5-triazine is 1,3,5-triazine-2,4,6-triamine, commonly known as melamine or cyanuramide. Another important derivative is 1,3,5-triazine-2,4,6-triol better known as cyanuric acid. Cyanuric chloride (2,4,6-trichloro-1,3,5-triazine) is the starting point for the manufacture of many herbicides such as Simazine and ...
In Canada, the use and sale of 2,4,5-T was prohibited after 1985. [5] The international trade of 2,4,5-T is restricted by the Rotterdam Convention. 2,4,5-T has since largely been replaced by dicamba and triclopyr. Human health effects from 2,4,5-T at low environmental doses or at biomonitored levels from low environmental exposures are unknown.
1,2,4,5-Tetrachloro-3-nitrobenzene ( tecnazene) is an organic compound with the formula HC6Cl4NO2. It is a colorless solid. A related isomer is 1,2,3,4-tetrachloro-5-nitrobenzene. It is used as a standard for quantitative analysis by nuclear magnetic resonance. [ 4][ 5] 1,2,4,5-Tetrachloro-3-nitrobenzene is also a fungicide used to prevent dry ...
The compound was first synthesized in 1924 by Oldřich Turek. [3] It can be prepared by the reaction of 1,3,5-trichloro-2,4,6-trinitrobenzene with sodium azide. 1,3,5-trichloro-2,4,6-trinitrobenzene is obtained from the nitration of 1,3,5-trichlorobenzene with nitric acid and sulfuric acid.
1,3,5-Trioxane, sometimes also called trioxane or trioxin, is a chemical compound with molecular formula C 3 H 6 O 3. It is a white, highly water-soluble solid with a chloroform -like odor. It is a stable cyclic trimer of formaldehyde , and one of the three trioxane isomers; its molecular backbone consists of a six-membered ring with three ...
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]
4-Phenyl-1,2,4-triazoline-3,5-dione (PTAD) is an azodicarbonyl compound. PTAD is one of the strongest dienophiles and reacts rapidly with dienes in Diels-Alder reactions. [ 1] The most prominent use of PTAD was the first synthesis of prismane in 1973. [ 2]