16294-60-3

Basic information

• Product Name: (3-Acenaphthoyl)propionicacid
• Synonyms: (3-Acenaphthoyl)propionicacid;γ-Oxo-5-acenaphthenebutyric acid
• CAS NO: 16294-60-3
• Molecular Formula: C₁₆H₁₄O₃
• Molecular Weight: 254.28056
• Mol File: 16294-60-3.mol

Chemical Properties

• Melting Point: 210 °C (dec.)(lit.)
• Boiling Point: 526.9°Cat760mmHg
• Flash Point: 286.5°C
• Appearance: /
• Density: 1.31g/cm³
• Vapor Pressure: 6.28E-12mmHg at 25°C
• Refractive Index: 1.67
• PKA: 4.54±0.17(Predicted)
• CAS DataBase Reference: (3-Acenaphthoyl)propionicacid(CAS DataBase Reference)
• NIST Chemistry Reference: (3-Acenaphthoyl)propionicacid(16294-60-3)
• EPA Substance Registry System: (3-Acenaphthoyl)propionicacid(16294-60-3)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36
• Hazardous Substances Data: 16294-60-3(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
(3-Acenaphthoyl)propionic acid is used as a building block for the synthesis of biologically active molecules and pharmaceuticals. Its incorporation into natural products can lead to the development of novel drugs and therapeutic agents, enhancing their efficacy and expanding their applications in medicine.
Used in Organic Synthesis:
(3-Acenaphthoyl)propionic acid is used as a key intermediate in the synthesis of complex organic compounds. Its unique structural features and reactivity make it a valuable component in the preparation of a wide range of chemical products.
Used in Materials Science:
(3-Acenaphthoyl)propionic acid is used as a component in the development of new materials with unique properties. Its structural features and reactivity contribute to the creation of innovative materials with potential applications in various industries.
Used in Chemical Technology:
(3-Acenaphthoyl)propionic acid is used in the development of new chemical processes and technologies. Its unique properties and reactivity can be harnessed to improve existing processes or enable the creation of new ones, driving innovation in the chemical industry.

InChI:InChI=1/C16H14O3/c17-14(8-9-15(18)19)12-7-6-11-5-4-10-2-1-3-13(12)16(10)11/h1-3,6-7H,4-5,8-9H2,(H,18,19)

Upstream product

• 108-30-5 succinic acid anhydride 
• 83-32-9 acenaphthene 
• 7446-70-0 aluminium trichloride 
• 98-95-3 nitrobenzene 

Downstream Products

• 7504-38-3 4-acenaphthen-5-yl-4-oxo-butyric acid methyl ester 
• 38036-08-7 4-acenaphthen-5-yl-butyric acid 
• 476-73-3 1,2,3,4-benzenetetracaboxylic acid 
• 28445-09-2 naphthalene-1,4,5-tricarboxylic acid 
• 518-02-5 1,2,5,6,7,8-hexahydrocyclohepta[fg]acenaphthylene 
• 76345-84-1 10,11-dihydro-3-phenylacephenanthro<8,7-d>pyrazole 
• 76345-82-9 10,11-dihydroacephenanthro<8,7-d>isoxazole 
• 7467-80-3 4,5,9,10-tetrahydro-8H-acephenanthrylen-7-one 

Relevant articles and documents

Condensed Heterocycles : Part VI - Synthesis of Dihydroacephenanthro-thiazoles, -isoxazole and -pyrazoles and Dihydroacenaphthocarbazoles

1-Oxo-1,2,3,4-tetrahydroacephenanthrene (I) has been converted to 2-amino-10,11-dihydroacephenanthrothiazole (III), 14(H)-aza-12,13-dihydroacenaphthocarbazole (IV), 10,11-dihydro-2-hydrazinoacephenanthrothiazole (V), 10,11-dihydroacephenanthroisoxazole (VII), 10,11-dihydroacephenanthropyrazole (VIII), 10,11-dihydro-3-phenylacephenanthropyrazole (IX), 10,11-dihydro-3-thiocarbamoylacephenanthropyrazole (X) and 12,13-dihydroacenaphthocarbazole (XII).