782-28-5

Basic information

• Product Name: 4-(2-Naphthyl)butanoic acid
• Synonyms: 2-NAPHTHALENEBUTYRIC ACID;4-(2-Naphthyl)Butyric Acid;2-Napthalenebutyricacid;2-Naphthalenebutanoic acid;4-(2-Naphthyl)butanoic acid;4-naphthalen-2-ylbutanoic acid
• CAS NO: 782-28-5
• Molecular Formula: C₁₄H₁₄O₂
• Molecular Weight: 214.26
• Mol File: 782-28-5.mol
• Article Data: 20

Chemical Properties

• Melting Point: 94-95 °C
• Boiling Point: 395.6 °C at 760 mmHg
• Flash Point: 292.5 °C
• Appearance: /
• Density: 1.164 g/cm³
• Vapor Pressure: 5.71E-07mmHg at 25°C
• Refractive Index: 1.618
• Solubility: Chloroform, DCM
• PKA: 4.75±0.10(Predicted)
• CAS DataBase Reference: 4-(2-Naphthyl)butanoic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(2-Naphthyl)butanoic acid(782-28-5)
• EPA Substance Registry System: 4-(2-Naphthyl)butanoic acid(782-28-5)

Safety Data

• Hazardous Substances Data: 782-28-5(Hazardous Substances Data)

Usage

Uses

2-Naphthalenebutanoic Acid is an intermediate in the synthesis of 4-Phenanthrol (P295015), a metabolite of Phenanthrene.

InChI:InChI=1/C14H14O2/c15-14(16)7-3-4-11-8-9-12-5-1-2-6-13(12)10-11/h1-2,5-6,8-10H,3-4,7H2,(H,15,16)

Upstream product

• 6326-90-5 ethyl 4-(naphthalen-2-yl)butanoate 
• 1590-22-3 4-(2-naphthyl)-4-oxobutyric acid 
• 854678-24-3 4-oxo-4-(5,6,7,8-tetrahydro-[2]naphthyl)-butyric acid methyl ester 
• 785-19-3 methyl 4-(naphthalen-2-yl)butanoate 
• 91-20-3 naphthalene 
• 625-38-7 but-3-enoic acid 
• 32316-92-0 naphthalene-2-boronic acid 
• 180037-65-4 γ-(2-naphthyl)-γ-butyrolactone 
• 2489-87-4 2-allylnaphthalene 
• 1955-35-7 5-(naphthalen-2-yl)furan-2(3H)-one 
• 785-17-1 4-oxo-4-(5,6,7,8-tetrahydronaphthalen-2-yl)butanoic acid 
• 782-27-4 4-(5,6,7,8-tetrahydronaphthalen-2-yl)butanoic acid 
• 785-18-2 methyl 4-(5,6,7,8-tetrahydronaphthalen-2-yl)butanoate 
• 119-64-2 tetralin 

Downstream Products

• 610-48-0 1-methylanthracene 
• 25177-45-1 4-Phenanthrylacetic acid 
• 85-01-8 phenanthrene 
• 7651-86-7 4-phenanthrol 
• 178556-70-2 4-(1-Trityl-1H-imidazol-4-yl)-1,2,3,4-tetrahydro-phenanthren-4-ol 
• 2657-44-5 4-(naphthalen-2-yl)butan-1-ol 

Relevant articles and documents

Preparation method of light-driven molecular motor based on oxidized benzofuran structure

The present invention relates to a preparation method and application of a molecular motor containing oxidized benzofuran structure, belonging to the field of organic chemistry technology. The first motor is based on 3-methyl-2,3-dihydrofyl-4(1H)-ketone and 2-coumarinone as raw materials, the second motor is based on 3-methyl-2,3-dihydrophenanthrene-4(1H)-keto and naphthalene [1,2-b]furan-2(3H)-ketone as raw materials, the third motor with 3-methyl-2,3-dihydrophenanthin-4 (1H)-keto and 6-isopropylphenone-2(3H)-keto as raw materials, in the presence of titanium tetrachloride and 1,8-diazoacyclodo-unicyclic-7-ene, In anhydrous tetrahydrofuran solvents, nucleophilic addition reactions are prepared. The reaction conditions of the present invention are mild, there is no need to add strong acids and strong bases, the equipment requirements are low, the operating cost is reduced; the reaction process produces less waste, the degree of environmental pollution is low; the obtained product motor structure is novel and has potential application value in the field of molecular devices.

Cationic α-Diimine Nickel and Palladium Complexes Incorporating Phenanthrene Substituents: Highly Active Ethylene Polymerization Catalysts and Mechanistic Studies of syn/ anti Isomerization

α-Diimine palladium complexes incorporating phenanthryl- and 6,7-dimethylphenanthrylimino groups have been synthesized and characterized. The (diimine)PdMeCl complexes prepared from 2,3-butanedione and acenaphthenequinone bearing the unsubstituted phenant

Carbonylative Transformation of Allylarenes with CO Surrogates: Tunable Synthesis of 4-Arylbutanoic Acids, 2-Arylbutanoic Acids, and 4-Arylbutanals

In this Communication, procedures for the selective synthesis of 4-arylbutanoic acids, 2-arylbutanoic acids, and 4-arylbutanals from the same allylbenzenes have been developed. With formic acid or TFBen as the CO surrogate, reactions proceed selectively and effectively under carbon monoxide gas-free conditions.