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1-Bromo-2-iodobenzene

Names

[ CAS No. ]:
583-55-1

[ Name ]:
1-Bromo-2-iodobenzene

[Synonym ]:
ortho-bromoiodobenzene
2-IODOBROMOBENZENE
1-bromo-2-iodo-benzen
1-Bromo-2-iodobenzene
2-BROMOINDAN-1-ONE
1-Brom-2-iodobenzene
O-BROMOIODOBENZENE
MFCD00001030
Benzene, 1-bromo-2-iodo-
2-Bromophenyl iodide
0-bromoiodobenzene
1,2-bromo-iodobenzene
1-iodo-2-bromobenzene
2-bromo-iodobenzene
1-bromo-2-iodo-benzene
EINECS 209-508-9

Chemical & Physical Properties

[ Density]:
2.2±0.1 g/cm3

[ Boiling Point ]:
249.7±13.0 °C at 760 mmHg

[ Melting Point ]:
9-10 °C(lit.)

[ Molecular Formula ]:
C6H4BrI

[ Molecular Weight ]:
282.904

[ Flash Point ]:
104.8±19.8 °C

[ Exact Mass ]:
281.854095

[ LogP ]:
3.93

[ Vapour Pressure ]:
0.0±0.5 mmHg at 25°C

[ Index of Refraction ]:
1.655

MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H315-H319-H335

[ Precautionary Statements ]:
P261-P305 + P351 + P338

[ Personal Protective Equipment ]:
Eyeshields;full-face respirator (US);Gloves;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter

[ Hazard Codes ]:
Xi:Irritant;

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S26-S36/37-S37/39

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2903999090

Precursor & DownStream

Customs

[ HS Code ]: 2903999090

[ Summary ]:
2903999090 halogenated derivatives of aromatic hydrocarbons VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:5.5% General tariff:30.0%

Articles

Stability-indicating reversed-phase HPLC method development and characterization of impurities in vortioxetine utilizing LC-MS, IR and NMR.

J. Pharm. Biomed. Anal. 117 , 325-32, (2015)

The current study reports the development and validation of a stability-indicating reversed phase HPLC method for the separation and identification of potential impurities in vortioxetine, a recently ...

Synthesis of carbazoles by intramolecular arylation of diarylamide anions.

J. Org. Chem. 74(12) , 4490-8, (2009)

The synthesis of a series of substituted 9H-carbazoles by the photostimulated S(RN)1 substitution reaction with diarylamines as starting substrate was performed. The diarylamines were obtained by two ...


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Related Compounds

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