2'-Nitroacetophenone, 97%
2'-Nitroacetophenone, 97%
2'-Nitroacetophenone, 97%
2'-Nitroacetophenone, 97%
Thermo Scientific Chemicals

2'-Nitroacetophenone, 97%

CAS: 577-59-3 | C8H7NO3 | 165.15 g/mol
製品番号(カタログ番号) A13208.09
または、製品番号A13208-09
価格(JPY)
-
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数量:
10 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
CAS577-59-3
IUPAC Name1-(2-nitrophenyl)ethan-1-one
Molecular FormulaC8H7NO3
InChI KeySUGXZLKUDLDTKX-UHFFFAOYSA-N
SMILESCC(=O)C1=CC=CC=C1[N+]([O-])=O
さらに表示
Assay from Suppliers CofA≥96.0% (U.S. specification)
Assay (GC)≥96.0% (non-U.S. specification)
Refractive Index1.5495-1.5545 @ 20°C (non-U.S. specification)
Appearance (Color)Clear yellow
FormLiquid
さらに表示
2'-Nitroacetophenone is an important raw material and intermediate used in Organic Synthesis, Pharmaceuticals, Agrochemicals and dyestuff. It is also used as a synthetic reagent. It is the sensitizer which can be used as pharmaceutical intermediates. It can also be used to produce 2-nitro-benzoic acid at temperature of 20°C.

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
2′-Nitroacetophenone is an important raw material and intermediate used in Organic Synthesis, Pharmaceuticals, Agrochemicals and dyestuff. It is also used as a synthetic reagent. It is the sensitizer which can be used as pharmaceutical intermediates. It can also be used to produce 2-nitro-benzoic acid at temperature of 20°C.

Solubility
It is Soluble in water, partly in ethanol, ether, chloroform, and ethyl acetate.

Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Stable under recommended storage conditions. Keep away from Strong oxidizing agents, Strong bases.
RUO – Research Use Only

General References:

  1. J. H. Boyer. Reduction of Organic Azides to Primary Amines with Lithium Aluminum Hydride. J. Am. Chem. Soc. 1951, 73, (12), 5865-5866.
  2. Masahito Watanabe .; Kunihiko Murata .; Takao Ikariya. Practical Synthesis of Optically Active Amino Alcohols via Asymmetric Transfer Hydrogenation of Functionalized Aromatic Ketones. J. Org. Chem.2002, 67, (5), 1712-1715.