Bromobenzene

Bromobenzene
Structure of bromobenzene	Space-filling model of bromobenzene
Names
	Preferred IUPAC name Bromobenzene
	Other names Phenyl Bromide; Bromobenzol; Monobromobenzene
Identifiers
CAS Number	108-86-1 ;
3D model (JSmol)	Interactive image;
Beilstein Reference	1236661
ChEBI	CHEBI:3179 ;
ChEMBL	ChEMBL16068 ;
ChemSpider	7673 ;
ECHA InfoCard	100.003.295
EC Number	203-623-8;
KEGG	C11036 ;
PubChem CID	7961;
RTECS number	CY9000000;
UNII	CO4D5J547L;
UN number	2514
CompTox Dashboard (EPA)	DTXSID5024637 ;
	InChI InChI=1S/C6H5Br/c7-6-4-2-1-3-5-6/h1-5H Key: QARVLSVVCXYDNA-UHFFFAOYSA-N ; InChI=1/C6H5Br/c7-6-4-2-1-3-5-6/h1-5H Key: QARVLSVVCXYDNA-UHFFFAOYAB;
	SMILES c1ccc(cc1)Br;
Properties
Chemical formula	C6H5Br
Molar mass	157.010 g·mol−1
Appearance	Colourless liquid
Odor	Pleasant aromatic odor
Density	1.495 g cm−3, liquid
Melting point	−30.8 °C (−23.4 °F; 242.3 K)
Boiling point	156 °C (313 °F; 429 K)
Solubility in water	0.041 g/100 mL
Solubility	soluble in diethyl ether, alcohol, CCl4; miscible in chloroform, benzene, petroleum ether
Vapor pressure	4.18 mm Hg
Magnetic susceptibility (χ)	-78.92·10−6 cm3/mol
Refractive index (nD)	1.5602
Viscosity	1.080 mPa·s at 25 °C; 1.124 mPa·s at 20 °C;
Hazards
	GHS labelling:
Pictograms
Signal word	Warning
Hazard statements	H226, H315, H411
Precautionary statements	P210, P233, P240, P241, P242, P243, P264, P273, P280, P302+P352, P303+P361+P353, P321, P332+P313, P362, P370+P378, P391, P403+P235, P501
NFPA 704 (fire diamond)	2 2 0
Flash point	51 °C (124 °F; 324 K)
Autoignition; temperature	565 °C (1,049 °F; 838 K)
Related compounds
Related halobenzenes	Fluorobenzene; Chlorobenzene; Iodobenzene
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). verify (what is ?) Infobox references

Bromobenzene is an aryl bromide and the simplest of the bromobenzenes, consisting of a benzene ring substituted with one bromine atom. Its chemical formula is C₆H₅Br. It is a colourless liquid although older samples can appear yellow. It is a reagent in organic synthesis.

^ Nomenclature of Organic Chemistry : IUPAC Recommendations and Preferred Names 2013 (Blue Book). Cambridge: The Royal Society of Chemistry. 2014. pp. 10, 31. doi:10.1039/9781849733069-00001. ISBN 978-0-85404-182-4.
^ Nayak, Jyoti N.; Aralaguppi, Mrityunjaya I.; Aminabhavi, Tejraj M. (2003). "Density, Viscosity, Refractive Index, and Speed of Sound in the Binary Mixtures of Ethyl Chloroacetate + Cyclohexanone, + Chlorobenzene, + Bromobenzene, or + Benzyl Alcohol at (298.15, 303.15, and 308.15) K". Journal of Chemical & Engineering Data. 48 (3): 628–631. doi:10.1021/je0201828. ISSN 0021-9568.

[iupac2013-1] Nomenclature of Organic Chemistry : IUPAC Recommendations and Preferred Names 2013 (Blue Book). Cambridge: The Royal Society of Chemistry. 2014. pp. 10, 31. doi:10.1039/9781849733069-00001. ISBN 978-0-85404-182-4.

[NayakAralaguppi2003-2] Nayak, Jyoti N.; Aralaguppi, Mrityunjaya I.; Aminabhavi, Tejraj M. (2003). "Density, Viscosity, Refractive Index, and Speed of Sound in the Binary Mixtures of Ethyl Chloroacetate + Cyclohexanone, + Chlorobenzene, + Bromobenzene, or + Benzyl Alcohol at (298.15, 303.15, and 308.15) K". Journal of Chemical & Engineering Data. 48 (3): 628–631. doi:10.1021/je0201828. ISSN 0021-9568.

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