89185-83-1

Basic information

• Product Name: 2,4-Pentanedione, 3-(4-nitrophenyl)-
• CAS NO: 89185-83-1
• Molecular Formula: C11H11NO4
• Molecular Weight: 221.213
• Mol File: 89185-83-1.mol
• Article Data: 12

Chemical Properties

• CAS DataBase Reference: 2,4-Pentanedione, 3-(4-nitrophenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2,4-Pentanedione, 3-(4-nitrophenyl)-(89185-83-1)
• EPA Substance Registry System: 2,4-Pentanedione, 3-(4-nitrophenyl)-(89185-83-1)

Safety Data

• Hazardous Substances Data: 89185-83-1(Hazardous Substances Data)

Usage

Physical form

Yellow crystalline powder

Solubility

Slightly soluble in water

Usage

Reagent in organic synthesis, production of pharmaceuticals and fine chemicals, manufacturing of dyes and pigments, potential applications in medicine

Hazards

Can be hazardous if not handled properly, precautions should be taken.

Upstream product

• 5332-96-7 1-(4-nitrophenyl)propan-2-one 
• 108-24-7 acetic anhydride 
• 586-78-7 para-nitrophenyl bromide 
• 123-54-6 acetylacetone 
• 636-98-6 p-nitrobenzene iodide 
• 456-27-9 4-nitrobenzenediazonium tetrafluoroborate 
• 132619-03-5 (E)-(4-Nitrophenyl)azo phenyl sulfide 

Downstream Products

• 1160169-23-2 (Z)-4-amino-3-(4-nitrophenyl)pent-3-en-2-one 
• 42418-61-1 3,5-dimethyl-4-(4-nitrophenyl)-1H-pyrazole 
• 1278456-10-2 C₁₄H₁₅NO₄ 
• 2155-99-9 4-(3,5-dimethylisoxazol-4-yl)aniline 
• 6159-25-7 1-<(4-nitro)-phenyl>-1,2-propandione 
• 1160169-37-8 1-(3-methyl-2-(4-nitrophenyl)-2H-azirin-2-yl)ethanone 
• 1377326-33-4 Ti₁₀O₂₄(isopropoxide)16(3-(4-nitrophenyl)pentane-2,4-dionato)4 
• 1331858-09-3 C₂₁H₂₁NO₃ 
• 1278456-17-9 C₁₆H₁₉NO₃ 
• 1331858-10-6 C₁₈H₂₃NO₃ 
• 1278456-12-4 C₁₅H₁₇NO₃ 
• 2155-98-8 3,5-dimethyl-4-(4-nitrophenyl)isoxazole 

Relevant articles and documents

SMALL MOLECULE MODULATORS OF IL-17

The present invention relates to a compound according to formula (I), (I) and pharmaceutically acceptable salts, hydrates, or solvates thereof. The invention further relates to said compounds for use in therapy, to pharmaceutical compositions comprising said compounds, to methods of treating diseases, e.g. dermal diseases, with said compounds, and to the use of said compounds in the manufacture of medicaments.

Iron-catalyzed aerobic oxidative cleavage of the C-C σ-bond using air as the oxidant: Chemoselective synthesis of carbon chain-shortened aldehydes, ketones and 1,2-dicarbonyl compounds

A simple iron-catalyzed aerobic oxidative C-C σ-bond cleavage of ketones has been developed. Readily available and environmentally benign air is used as the oxidant. This reaction avoids the use of noble metal catalysts or specialized oxidants, chemoselectively yielding carbon chain-shortened aldehydes, ketones and 1,2-dicarbonyl compounds without overoxidation.

Copper(II) and 1,1′-trimethylene-2,2′-biimidazole-promoted arylation of acetylacetone with aryl iodides

A new and efficient way was developed to carry out the reaction of acetylacetone with aryl iodides under the assistance of Cu(II) and 1,1′-trimethylene-2,2′-biimidazole at 100°C. 3-Aryl-2,4-pentanediones were obtained in excellent yields. Copyright