1-Bromo-2-nitrobenzene

1-Bromo-2-nitrobenzene
  • CAS No.:577-19-5
Other grades of this product :
1-Bromo-2-nitrobenzene Basic information
Product Name:1-Bromo-2-nitrobenzene
Synonyms:Benzene,1-bromo-2-nitro-;o-Nitrophenyl bromide;1-Bromo-2-nitrobenzene,98%;2-Bromonitrobenzene 98%;1-Bromo-2-nitrobenze;1-BROMO-2-NITROBENZENE FOR SYNTHESIS;1-BroMo-2-Nitrobenzene, Ultrapure;2- broMinenitrobenzene
CAS:577-19-5
MF:C6H4BrNO2
MW:202.01
EINECS:209-409-0
Product Categories:Aromatic Hydrocarbons (substituted) & Derivatives;Benzene derivates;Miscellaneous;Bromine Compounds;Nitro Compounds;Nitro Compounds;Nitrogen Compounds;Organic Building Blocks
Mol File:577-19-5.mol
1-Bromo-2-nitrobenzene Chemical Properties
Melting point 40-42 °C (lit.)
Boiling point 261 °C (lit.)
density 1.7 g/cm3 (20℃)
refractive index 1.6060 (estimate)
Fp >230 °F
storage temp. 2-8°C
form powder to crystal
color Light yellow to Amber to Dark green
Water Solubility insoluble
BRN 2044109
Stability:Stable. Combustible. Incompatible with strong bases, strong oxidizing agents.
CAS DataBase Reference577-19-5(CAS DataBase Reference)
NIST Chemistry ReferenceBenzene, 1-bromo-2-nitro-(577-19-5)
EPA Substance Registry Systemo-Bromonitrobenzene (577-19-5)
Safety Information
Hazard Codes Xn,Xi
Risk Statements 20/21/22-36/37/38-22
Safety Statements 36/37-36/37/39-26-22
RIDADR UN 3459 6.1/PG 3
WGK Germany 3
RTECS CY9040450
Hazard Note Irritant
TSCA Yes
HazardClass 6.1
PackingGroup III
HS Code 29049085
MSDS Information
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1-Bromo-2-nitrobenzene Usage And Synthesis
Chemical Propertieswhite to light yellow crystal powder
Uses1-Bromo-2-nitrobenzene is used in organic synthesis. It also can react with 2-methylamino-benzoic acid to get N-methyl-N-(2-nitro-phenyl)-anthranilic acid. And it is also used in the preparation of 4-methoxy-2?-nitrodiphenyl ether, 1-methoxy-3,5-bis-(2-nitro-phenoxy)benzene.
Uses1-Bromo-2-nitrobenzene may be used in the preparation of:
  • 4-methoxy-2′-nitrodiphenyl ether
  • 1-methoxy-3,5-bis-(2-nitro-phenoxy)benzene
  • 5-hydroxy-3-methoxy-2′-nitrodiphenyl ether
General Description1-Bromo-2-nitrobenzene undergoes palladium[0]-mediated Ullmann cross-coupling reaction with a range of β-halo-enals, -enones or -esters to afford the corresponding β-aryl derivatives. Palladium[0]-mediated Ullmann cross-coupling reaction of 1-bromo-2-nitrobenzene with β-bromo-α,β-unsaturated aldehydes is reported.
Purification MethodsCrystallise it twice from pet ether, using charcoal before the first crystallisation. [Beilstein 5 III 618, 5 IV 728.]

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