CAS 17408-15-0
:2-nitropropiophenone
Description:
2-Nitropropiophenone is an organic compound characterized by its structure, which includes a nitro group (-NO2) and a ketone functional group (C=O) within a propiophenone framework. It typically appears as a yellow crystalline solid and is known for its aromatic properties due to the presence of a phenyl ring. The compound is often used in organic synthesis and can serve as an intermediate in the production of various pharmaceuticals and agrochemicals. Its reactivity is influenced by the electron-withdrawing nature of the nitro group, which can enhance electrophilic substitution reactions on the aromatic ring. Additionally, 2-nitropropiophenone may exhibit moderate solubility in organic solvents, while its solubility in water is limited. Safety considerations are important when handling this compound, as it may pose health risks if inhaled or ingested, and appropriate safety measures should be taken to minimize exposure. Overall, 2-nitropropiophenone is a valuable compound in synthetic organic chemistry with distinct physical and chemical properties.
Formula:C9H9NO3
InChI:InChI=1/C9H9NO3/c1-2-9(11)7-5-3-4-6-8(7)10(12)13/h3-6H,2H2,1H3
SMILES:CCC(=O)c1ccccc1N(=O)=O
Synonyms:- 1-(2-Nitrophenyl)Propan-1-One
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Found 2 products.
1-(2-Nitrophenyl)propan-1-one
CAS:<p>1-(2-Nitrophenyl)propan-1-one is an electron acceptor in the chemistry of isoxazoles. The compound has a cation that can be protonated to form an alkyl group. 1-(2-Nitrophenyl)propan-1-one has been shown to react with cyanide to form acylium ions and release hydrogen cyanide gas. This compound also reacts with the probe pinacolborane to form isopropyl boronate, which can be used as a spectroscopic probe for aromatic ketones.</p>Formula:C9H9NO3Purity:Min. 95%Molecular weight:179.17 g/mol
