55902-35-7

Basic information

• Product Name: (Z)-4-Phenyl-3-nitro-3-buten-2-one
• Synonyms: (Z)-4-Phenyl-3-nitro-3-buten-2-one
• CAS NO: 55902-35-7
• Molecular Formula: C₁₀H₉NO₃
• Molecular Weight: 191.18
• Mol File: 55902-35-7.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 331.2°Cat760mmHg
• Flash Point: 159.1°C
• Appearance: /
• Density: 1.193g/cm³
• Vapor Pressure: 0.000158mmHg at 25°C
• Refractive Index: 1.555
• CAS DataBase Reference: (Z)-4-Phenyl-3-nitro-3-buten-2-one(CAS DataBase Reference)
• NIST Chemistry Reference: (Z)-4-Phenyl-3-nitro-3-buten-2-one(55902-35-7)
• EPA Substance Registry System: (Z)-4-Phenyl-3-nitro-3-buten-2-one(55902-35-7)

Safety Data

• Hazardous Substances Data: 55902-35-7(Hazardous Substances Data)

Usage

Description

(Z)-4-Phenyl-3-nitro-3-buten-2-one, with the molecular formula C10H9NO3, is a chemical compound characterized by its yellow to orange crystalline appearance. It is an α,β-unsaturated ketone, which means it has a carbonyl group and an adjacent double bond in its structure. (Z)-4-Phenyl-3-nitro-3-buten-2-one is known for its reactivity and ability to undergo various chemical transformations, making it a versatile building block in the synthesis of pharmaceuticals and other organic compounds.

Uses

Used in Pharmaceutical Synthesis:
(Z)-4-Phenyl-3-nitro-3-buten-2-one is used as a key intermediate in the pharmaceutical industry for the synthesis of various drugs. Its unique structure allows for the creation of complex molecules that can be utilized in the development of new medications.
Used in Organic Chemistry Research:
In research laboratories, (Z)-4-Phenyl-3-nitro-3-buten-2-one serves as a starting material for the synthesis of a wide range of organic compounds. Its reactivity and ability to undergo multiple chemical transformations make it a valuable tool for exploring new chemical reactions and developing novel organic molecules.
Used in Chemical Industries:
(Z)-4-Phenyl-3-nitro-3-buten-2-one is also employed in the chemical industry as a building block for the production of complex molecules. Its versatility and reactivity contribute to the development of new materials and compounds with potential applications in various fields, such as materials science, agriculture, and environmental science.

InChI:InChI=1/C10H9NO3/c1-8(12)7-10(11(13)14)9-5-3-2-4-6-9/h2-7H,1H3/b10-7-

Upstream product

• 1896-62-4 (E)-benzalacetone 
• 10230-68-9 1-nitro-2-propanone 
• 1077-18-5 N-benzylidenebutan-1-amine 

Downstream Products

• 91251-46-6 amino-3 phenyl-4 butanol-2 
• 5440-27-7 3-amino-4-phenyl-2-butanone hydrochloride 
• 71087-75-7 (E)-3-(hydroxyimino)-4-phenylbutan-2-one 
• 134777-63-2 6-dimethyl-5-nitro-4-phenyl-2-oxo-1,2,3,4-tetrahydropyrimidine 
• 154355-41-6 1,4-dihydro-6-methyl-2-methoxy-5-nitro-4-phenylpyrimidine 
• 152192-71-7 1,6-dimethyl-5-nitro-4-phenyl-2-oxo-1,2,3,4-tetrahydropyrimidine 
• 1116578-88-1 4-(1-methylpyrrol-2-yl)-3-nitro-4-phenylbutan-2-one 
• 56426-41-6 3-methyl-5-phenylpyrazole 
• 59067-31-1 1-(5-phenyl-2H-1,2,3-triazol-4-yl)ethan-1-one 
• 940-48-7 benzaldehyde acetylhydrazone 
• 292617-98-2 2,6-dimethyl-5-nitro-4-phenyl-nicotinonitrile 
• 165289-42-9 2,6-dimethyl-3-nitro-4-phenyl-5-ethoxycarbonyl-1,4-dihydropyridine 

Relevant articles and documents

Nitropyridines. 2*. Hantzsch synthesis of nitro- and dinitropyridines

The interaction of α, β-unsaturated nitro ketones and various enamines leads to the synthesis of 5-nitro-1,4-dihydropyridines containing acetyl, amide, benzoyl, ester, and cyano groups in position 3, and also unsymmetrical 3,5-dinitro-1,4-dihydropyridines

Preparation, reduction chimique et electrochimique d'α-nitrostyrylcetones - synthese d'heterocycles azotes

Nitration of styryl ketones with nitrogen peroxide leads to the corresponding α-nitroethylenic ketones in good yield.However, the presence of methoxy groups involves a nitration on the aromatic nucleus.LiAlH4 reduction of α-nitrostyrylketones yields the c