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[108-36-1] [106-37-6] Properties Density and phase: 1.9940 g/ml, liquid 1.9523 g/ml, liquid 1.84 g/ml, solid Solubility in water: practically insoluble Other solubilities Soluble in 70 parts ethanol. Soluble in benzene, chloroform and very soluble in diethyl ether. Melting point: 7.1 °C −7.0 °C 87 °C Boiling point: 225 °C 218–220 °C ...
Monobromotoluene isomers [1] [2] [3] Common name Structure Systematic name: 1-bromo-2-methylbenzene 1-bromo-3-methylbenzene 1-bromo-4-methylbenzene Molecular formula: C 7 H 7 Br (C 6 H 4 BrCH 3) Molar mass: 171.03 g/mol Appearance colorless liquid colorless liquid white crystalline solid CAS number [95-46-5] [591-17-3]
It is a brominated aromatic chemical used principally for giving flame retardant properties to materials. [1] It is TSCA and REACH registered and has the molecular formula C 21 H 20 Br 4 O 4 . The IUPAC name is 2-{[2,6-dibromo-4-(2-{3,5-dibromo-4-[(oxiran-2-yl)methoxy]phenyl}propan-2-yl)phenoxy]methyl}oxirane.
This reagent can be used, e.g. in the reaction with carbon dioxide to prepare benzoic acid. [4] Other methods involve palladium-catalyzed coupling reactions , such as the Suzuki reaction . Bromobenzene is used as a precursor in the manufacture of phencyclidine .
Bromoform was discovered in 1832 by Löwig who distilled a mixture of bromal and potassium hydroxide, as analogous to preparation of chloroform from chloral. [5]Bromoform can be prepared by the haloform reaction using acetone and sodium hypobromite, by the electrolysis of potassium bromide in ethanol, or by treating chloroform with aluminium bromide.
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2-hydroxybenzene 3,4-Dibromophenol, 1,2-Dibromo-4-hydroxybenzene 3,5-Dibromophenol, 1,3-Dibromo-5-hydroxybenzene Structural formula: CAS Number: 57383-80-9: 615-58-7: 28165-52-8: 608-33-3: 615-56-5: 626-41-5 PubChem: CID 34264 from PubChem: CID 12005 from PubChem: CID 34177 from PubChem: CID 11847 from PubChem: CID 12003 from PubChem: CID 12280 ...
1-Bromo-3-chlorobenzene: by (3-chlorophenyl)trimethylgermanium by electrophilic substitution [2] [better source needed] 1-Bromo-4-chlorobenzene: From a derivative of (4-bromophenyl)silane using N-bromosuccinimide [3] From 4-chlorophenol using triphenylphosphine dibromide [4] or phenylphosphorus tetrachloride [5]
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