19926-49-9

Basic information

• Product Name: ETHYL BIPHENYL-2-CARBOXYLATE
• Synonyms: RARECHEM AL BI 0859;ETHYL BIPHENYL-2-CARBOXYLATE;[1,1'-Biphenyl]-2-carboxylic acid, ethyl ester;Ethyl 2-phenylbenzoate
• CAS NO: 19926-49-9
• Molecular Formula: C₁₅H₁₄O₂
• Molecular Weight: 226.27
• Mol File: 19926-49-9.mol
• Article Data: 33

Chemical Properties

• Boiling Point: 360.751°C at 760 mmHg
• Flash Point: 165.202°C
• Appearance: /
• Density: 1.082g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.556
• CAS DataBase Reference: ETHYL BIPHENYL-2-CARBOXYLATE(CAS DataBase Reference)
• NIST Chemistry Reference: ETHYL BIPHENYL-2-CARBOXYLATE(19926-49-9)
• EPA Substance Registry System: ETHYL BIPHENYL-2-CARBOXYLATE(19926-49-9)

Safety Data

• Hazardous Substances Data: 19926-49-9(Hazardous Substances Data)

Usage

General Description

Ethyl biphenyl-2-carboxylate is a chemical compound used primarily as a fragrance ingredient and flavoring agent in various consumer products. It is a colorless to pale yellow liquid with a sweet, floral odor. Ethyl biphenyl-2-carboxylate is commonly used in perfumes, soaps, lotions, and other personal care products, as well as in food and beverage flavorings. It is also used as a solvent and a chemical intermediate in the production of other compounds. However, it is important to handle ethyl biphenyl-2-carboxylate with caution as it may cause skin and eye irritation and should be stored and used in a well-ventilated area.

InChI:InChI=1/C15H14O2/c1-2-17-15(16)14-11-7-6-10-13(14)12-8-4-3-5-9-12/h3-11H,2H2,1H3

Upstream product

• 64-17-5 ethanol 
• 947-84-2 2-Biphenylcarboxylic acid 
• 93-89-0 benzoic acid ethyl ester 
• 100-34-5 benzene diazonium chloride 
• 1829-28-3 ethyl 2-iodobenzoate 
• 100-59-4 phenylmagnesium chloride 
• 6091-64-1 2-bromobenzoic acid ethyl ester 
• 7335-25-3 ethyl 2-chlorobenzoate 
• 62673-29-4 phenyl(diisobutyl)aluminium 
• 2216-94-6 phenylpropynoic acid ethyl ester 
• 1165952-91-9 cyclohexa-1,3-diene 
• 104-55-2 3-phenyl-propenal 
• 98-80-6 phenylboronic acid 
• 443-26-5 2-fluoro-benzoic acid ethyl ester 

Downstream Products

• 486-25-9 9-fluorenone 
• 154660-48-7 [1,1′-biphenyl]-2-carbohydrazide 
• 2928-43-0 2-biphenylmethanol 
• 92-52-4 biphenyl 
• 947-84-2 2-Biphenylcarboxylic acid 

Relevant articles and documents

Synthesis, characterization and computational evaluation of bicyclooctadienes towards molecular solar thermal energy storage

Molecular solar-thermal energy storage (MOST) systems are based on photoswitches that reversibly convert solar energy into chemical energy. In this context, bicyclooctadienes (BODs) undergo a photoinduced transformation to the corresponding higher energy

Regioselective synthesis of substituted cyclohexa-1,3-dienes via the base-mediated cyclisation of α,β-unsaturated carbonyl compounds and γ-phosphonylcrotonates

The base-mediated reaction of α,β-unsaturated carbonyl compounds and γ-phosphonylcrotonates under an argon atmosphere readily furnishes substituted cyclohexa-1,3-dienes. The cyclisation proceeds with complete regioselectivity to afford products that are r

Base-free Pd-MOF catalyzed the Suzuki-Miyaura cross-coupling reaction of arenediazonium tetrafluoroborate salts with arylboronic acids

A convenient and environmental benign synthesis of biaryls has been demonstrated by a straightforward reaction catalyzed by the palladium-containing metal-organic framework (Pd-MOF) [Pd (2-pymo)2]n (2-pymo = 2-pyrimidinolate). A series of functionalized biaryl derivatives have been synthesized in good to excellent yields by the Suzuki-miyaura cross-couplings of sustainable arenediazonium salts with a variety of arylboronic acids and the reactions were catalyzed by the Pd-MOF using methanol as a benign solvent. Those base- and additive-free catalytic reactions proceeded smoothly under non-anhydrous and non-degassed condition. Such transformation avoided high reaction temperature, tolerated many functional groups and presented a wide substrate scope. The catalyst could be recovered by filtration and reused for four successive cycles before collapse of the MOF structure.