1-Fluoro-2-nitrobenzene, 99%
1-Fluoro-2-nitrobenzene, 99%
1-Fluoro-2-nitrobenzene, 99%
Thermo Scientific Chemicals

1-Fluoro-2-nitrobenzene, 99%

CAS: 1493-27-2 | C6H4FNO2 | 141.101 g/mol
数量:
50 g
250 g
1000 g
製品番号(カタログ番号) A13852.0B
または、製品番号A13852-0B
価格(JPY)
-
数量:
1000 g
一括またはカスタム形式をリクエストする
化学物質識別子
CAS1493-27-2
IUPAC Name1-fluoro-2-nitrobenzene
Molecular FormulaC6H4FNO2
InChI KeyPWKNBLFSJAVFAB-UHFFFAOYSA-N
SMILES[O-][N+](=O)C1=CC=CC=C1F
さらに表示
Identification (FTIR)Conforms
Assay (GC)≥98.5%
Refractive Index1.5300-1.5330 @ 20?C
Appearance (Color)Clear yellow to orange to brown
FormLiquid
1-Fluoro-2-nitrobenzene is an intermediate in the synthetic preparations of various pharmaceutical goods.

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-Fluoro-2-nitrobenzene is an intermediate in the synthetic preparations of various pharmaceutical goods.

Solubility
Immiscible in water.

Notes
Avoid excessive heat and light.
RUO – Research Use Only

General References:

  1. Elaine K. Fukuda; Robert T. McIverJr. Relative electron affinities of substituted benzophenones, nitrobenzenes, and quinones.J. Am. Chem. Soc.1985, 107 (8), 2291-2296.
  2. The activating effect of aryl halides by o- or p-nitro groups is most pronounced for aryl fluorides, e.g. reacts readily with arylamines in a convenient synthesis of 2-nitrodiarylamines: Synthesis, 215 (1980).