Dibromochloromethane

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Dibromochloromethane


Preferred IUPAC name Dibromochloromethane^{[citation needed]}
Systematic name Dibromo(chloro)methane^[1]
Other names Chlorodibromomethane^{[citation needed]} Monochlorodibromomethane^{[citation needed]}
Identifiers
Abbreviations	CDBM^{[citation needed]}
CAS number	124-48-1^Y
PubChem	31296
ChemSpider	29036^Y
EC number	204-704-0
KEGG	C14692^Y
MeSH	chlorodibromomethane
ChEMBL	CHEMBL157093^Y
RTECS number	PA6360000
Beilstein Reference	1731046
Jmol-3D images	Image 1
SMILES ClC(Br)Br
InChI InChI=1S/CHBr2Cl/c2-1(3)4/h1H^Y Key: GATVIKZLVQHOMN-UHFFFAOYSA-N^Y
Properties
Molecular formula	CHBr₂Cl
Molar mass	208.28 g mol⁻¹
Appearance	Colorless liquid
Density	2.451 g mL⁻¹
Melting point	−22 °C; −8 °F; 251 K
Boiling point	119 to 120 °C; 246 to 248 °F; 392 to 393 K (at 99.7 kPa)
log P	2.206
k_H	8.6 μmol Pa⁻¹ kg⁻¹
Refractive index (n_D)	1.547
Hazards
GHS pictograms
GHS signal word	WARNING
GHS hazard statements	H302
EU classification	Xn
R-phrases	R22
LD₅₀	370 mg kg⁻¹ (oral, rat)
Related compounds
Related alkanes	Chloromethane Chloroiodomethane Bromochloromethane
Related compounds	2-Chloroethanol
Y (verify) (what is: Y/N?) Except where noted otherwise, data are given for materials in their standard state (at 25 °C (77 °F), 100 kPa)
Infobox references

Dibromochloromethane is a compound with formula CHBr₂Cl. It is a trihalomethane.

Dibromochloromethane was formerly used as a flame retardant and as an intermediate in chemicals manufacturing. Today it is used only as a laboratory reagent.

Small quantities of dibromochloromethane are produced in ocean by algae.

References

↑ "chlorodibromomethane - Compound Summary". PubChem Compound. USA: National Center Biotechnology Information. 27 March 2005. Identification. Retrieved 24 June 2012.

External links

v t e Halomethanes

Monosubstituted	CH₃F CH₃Cl CH₃Br CH₃I

Disubstituted	CH₂F₂ CH₂ClF CH₂BrF CH₂FI CH₂Cl₂ CH₂BrCl CH₂ClI CH₂Br₂ CH₂BrI CH₂I₂

Trisubstituted	CHF₃ CHClF₂ CHBrF₂ CHF₂I CHCl₂F CHBrClF CHClFI CHBr₂F CHBrFI CHFI₂ CHCl₃ CHBrCl₂ CHCl₂I CHBr₂Cl CHBrClI CHClI₂ CHBr₃ CHBr₂I CHBrI₂ CHI₃

Tetrasubstituted	CF₄ CClF₃ CBrF₃ CF₃I CCl₂F₂ CBrClF₂ CClF₂I CBr₂F₂ CBrF₂I CF₂I₂ CCl₃F CBrCl₂F CCl₂FI CBr₂ClF C*BrClFI CClFI₂ CBr₃F CBr₂FI CBrFI₂ CFI₃ CCl₄ CBrCl₃ CCl₃I CBr₂Cl₂ CBrCl₂I CCl₂I₂ CBr₃Cl CBr₂ClI CBrClI₂ CClI₃ CBr₄ CBr₃I CBr₂I₂ CBrI₃ CI₄

* Chiral compound.

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