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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 .
Tribromobenzene isomers Common name and systematic name 1,2,3-Tribromobenzene [1] [2] 1,2,4-Tribromobenzene [3] [4] 1,3,5-Tribromobenzene [5] [6] Structure Molecular formula: C 6 H 3 Br 3: Molar mass: 314.802 g/mol Appearance colorless solid CAS number [608-21-9] [615-54-3] [626-39-1] Properties Solubility in water: practically insoluble ...
1,3,5-Tribromobenzene This page was last edited on 1 February 2024, at 18:49 (UTC). Text is available under the Creative Commons Attribution-ShareAlike 4.0 ...
3), tetrabutylammonium iodide (TBAI) as a phase-transfer catalyst, and sodium hydroxide as a base. Below is an example reaction of 1,3-dibromobenzene to isophthalic acid . [ 1 ]
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.
1,3,5-Trinitrobenzene is one of three isomers of trinitrobenzene with the formula C 6 H 3 (NO 2) 3. A pale yellow solid, the compound is highly explosive. [2]
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.
Trichlorobenzene (TCB) may refer to any of three isomeric chlorinated derivatives of benzene with the molecular formula C 6 H 3 Cl 3. They differ by the positions of the chlorine atoms around the ring: 1,2,3-Trichlorobenzene; 1,2,4-Trichlorobenzene; 1,3,5-Trichlorobenzene
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