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1.208 g mL −1 [2] Boiling point: 118–119 °C; 244–246 °F; 391–392 K Hazards GHS labelling: Pictograms. Hazard statements. H225, H315, H319, H335:
2-Bromophenol: 3-Bromophenol: 4-Bromophenol: Other names o-Bromophenol: m-Bromophenol: p-Bromophenol Chemical structure: CAS number: 95-56-7: 591-20-8: 106-41-2 PubChem ID CID 7244 from PubChem: CID 11563 from PubChem: CID 7808 from PubChem: Chemical formula: C 6 H 5 BrO Molar mass: 173.02 g/mol 1: Physical state: liquid solid Melting point: 3 ...
2-Bromopentane [1] (chiral) 3-Bromopentane; There are four isomers of monobromopentane based on 2-methylbutane: 1-Bromo-2-methylbutane (chiral) 1-Bromo-3-methylbutane; 2-Bromo-2-methylbutane; 2-Bromo-3-methylbutane (chiral) 2,2-Dimethylpropane has only one monobrominated derivative, 1-bromo-2,2-dimethylpropane, also known as neopentyl bromide. [2]
Iodobenzene reacts with chlorine to give the complex, iodobenzene dichloride, [4] which is used as a solid source of chlorine. Iodobenzene can also serve as a substrate for the Sonogashira coupling, Heck reaction, and other metal-catalyzed couplings. These reactions proceed via the oxidative addition of iodobenzene.
Such reactions give alkenes in the case of vicinal alkyl dihalides: [2] R 2 C(X)C(X)R 2 + M → R 2 C=CR 2 + MX 2. Most desirable from the perspective of remediation are dehalogenations by hydrogenolysis, i.e. the replacement of a C−X bond by a C−H bond. Such reactions are amenable to catalysis: R−X + H 2 → R−H + HX
1-Bromo-4-iodobenzene is a mixed aryl halide (aryl bromide and aryl iodide) with the formula BrC 6 H 4 I. [2] Preparation.
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]
There are six structural isomers, each with the molecular formula C 6 H 4 Br 2 O, which differ by arrangement of the substituents. Dibromophenols: Name 2,3-Dibromophenol,