13080-43-8

Basic information

• Product Name: BETA-NAPHTHYL PROPIONATE
• Synonyms: BETA-NAPHTHYL PROPIONATE;BETA-NAP-PROPIONATE;2-NAPHTHYL PROPIONATE;PROPIONIC ACID BETA-NAPHTHYL ESTER;PROPIONIC ACID 2-NAPHTHYL ESTER;2-Naphthalenol, propanoate;B-naphthyl propionate;Propanoic acid 2-naphtyl ester
• CAS NO: 13080-43-8
• Molecular Formula: C₁₃H₁₂O₂
• Molecular Weight: 200.23
• EINECS: 235-984-2
• Mol File: 13080-43-8.mol
• Article Data: 9

Chemical Properties

• Melting Point: 48-51 °C
• Boiling Point: 324 °C at 760 mmHg
• Flash Point: 113.8 °C
• Appearance: /
• Density: 1.126 g/cm³
• Vapor Pressure: 0.000253mmHg at 25°C
• Refractive Index: 1.591
• Storage Temp.: −20°C
• CAS DataBase Reference: BETA-NAPHTHYL PROPIONATE(CAS DataBase Reference)
• NIST Chemistry Reference: BETA-NAPHTHYL PROPIONATE(13080-43-8)
• EPA Substance Registry System: BETA-NAPHTHYL PROPIONATE(13080-43-8)

Safety Data

• WGK Germany: 3
• Hazardous Substances Data: 13080-43-8(Hazardous Substances Data)

Usage

General Description

BETA-NAPHTHYL PROPIONATE is a chemical compound that falls under the category of alpha-keto acids and derivatives. It is commonly used as a flavoring agent in the food and beverage industry, adding a floral and fruity aroma to various products. BETA-NAPHTHYL PROPIONATE is also utilized in the production of perfumes and fragrances, as well as in the pharmaceutical industry for its potential physiological effects. Additionally, it has shown promise as a potential inhibitor of prostate cancer cell growth, leading to its investigation as a potential therapeutic agent for cancer treatment. Overall, BETA-NAPHTHYL PROPIONATE serves various commercial and scientific purposes, making it a versatile and useful chemical compound.

InChI:InChI=1/C13H12O2/c1-2-13(14)15-12-8-7-10-5-3-4-6-11(10)9-12/h3-9H,2H2,1H3

Upstream product

• 110-86-1 pyridine 
• 123-62-6 propionic acid anhydride 
• 135-19-3 β-naphthol 
• 79-03-8 propionyl chloride 
• 802294-64-0 propionic acid 
• 74-85-1 ethene 
• 18052-85-2 2-naphthyltrimethylsilane 
• 109-52-4 valeric acid 
• 79-31-2 isobutyric Acid 
• 98-89-5 Cyclohexanecarboxylic acid 
• 1759-53-1 cyclopropanecarboxylic acid 
• 65-85-0 benzoic acid 
• 105-38-4 vinyl propionate 

Downstream Products

• 612-94-2 2-phenylnaphthalene 
• 135-19-3 β-naphthol 

Relevant articles and documents

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An extremely efficient and green method for the acylation of secondary alcohols, phenols and naphthols with a deep eutectic solvent as the catalyst

The typical deep eutectic solvent [CholineCl][ZnCl2]3, easily prepared from choline chloride and zinc chloride, is green and useful for the acylation of secondary alcohols, phenols, and naphthols with acid anhydrides. Its efficiency allows the acylation of sterically hindered secondary alcohols and acid anhydrides to proceed in high yield under mild condition. The catalyst is cheap, easy to handle, conveniently synthesized in a single step, and recyclable for several times without significant loss of catalytic activity.

Asymmetric cycloadditions of o-quinone methides employing chiral ammonium fluoride precatalysts

(Chemical Equation Presented) The catalytic, enantioselective, [4+2] cycloaddition reaction of ortho-quinone methides with silyl ketene acetals is described. This mechanistically interesting reaction, initiated by a chiral cinchona alkaloid-derived ammonium fluoride "precatalyst" complex, affords a variety of alkyl- and aryl-substituted 3,4-dihydrocoumarin products in excellent yield and with good enantioselectivity.