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Thermo Scientific Chemicals
1-Bromo-2-nitrobenzene, 99%
CAS: 577-19-5 | C6H4BrNO2 | 202.007 g/mol
化学物質識別子
CAS577-19-5
IUPAC Name1-bromo-2-nitrobenzene
Molecular FormulaC6H4BrNO2
InChI KeyORPVVAKYSXQCJI-UHFFFAOYSA-N
SMILES[O-][N+](=O)C1=CC=CC=C1Br
さらに表示
仕様
スペックシート
スペックシートFormCrystalline or fused solid, lumps or powder
Appearance (Color)Pale yellow to orange or brown
Identification (FTIR)Conforms
Assay (GC)≥98.5%
Melting Point (clear melt)38-44?C
1-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.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
1-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.
Solubility
Insoluble in water.
Notes
Store away from strong oxidizing agents. Keep container tightly closed. Store in cool, dry conditions in well sealed containers.
1-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.
Solubility
Insoluble in water.
Notes
Store away from strong oxidizing agents. Keep container tightly closed. Store in cool, dry conditions in well sealed containers.
RUO – Research Use Only
Surajit Some.; Jayanta K. Ray.; Martin G. Banwell.; Matthew T. Jones. Fein. New protocols for the synthesis of 3,4-annulated and 4-substituted quinolines from β-bromo-α,β-unsaturated aldehydes and 1-bromo-2-nitrobenzene or 2-bromoacetanilide. Tetrahedron Letters. 2007, 48, (20), 3609-3612.