722-01-0

Basic information

• Product Name: PHENYL PHENYLACETATE
• Synonyms: PHENYL-ACETIC ACID PHENYL ESTER;PHENYL PHENYLACETATE;Benzeneacetic acid, phenyl ester;2-Phenylacetic acid (phenyl) ester;Phenyl benzeneacetate;Phenyl phenylacetate 96%
• CAS NO: 722-01-0
• Molecular Formula: C₁₄H₁₂O₂
• Molecular Weight: 212.24
• Product Categories: C12 to C63;Carbonyl Compounds;Esters;Bioactive Small Molecules;Building Blocks;C12 to C63;Carbonyl Compounds;Cell Biology;Chemical Synthesis;Organic Building Blocks;P
• Mol File: 722-01-0.mol
• Article Data: 41

Chemical Properties

• Melting Point: 40-42 °C(lit.)
• Boiling Point: 158 °C7 mm Hg(lit.)
• Flash Point: >230 °F
• Appearance: /
• Density: 1.1035 (rough estimate)
• Vapor Pressure: 6.11E-05mmHg at 25°C
• Refractive Index: 1.5570 (estimate)
• CAS DataBase Reference: PHENYL PHENYLACETATE(CAS DataBase Reference)
• NIST Chemistry Reference: PHENYL PHENYLACETATE(722-01-0)
• EPA Substance Registry System: PHENYL PHENYLACETATE(722-01-0)

Safety Data

• WGK Germany: 3
• Hazardous Substances Data: 722-01-0(Hazardous Substances Data)

Usage

General Description

Phenyl phenylacetate is a chemical compound with the molecular formula C14H14O2. It is an aromatic ester that is commonly used in the synthesis of pharmaceuticals, fragrances, and flavors. Phenyl phenylacetate is also known for its potential use as a biomarker for monitoring oxidative stress in biological samples. Additionally, it has been studied for its potential anti-inflammatory and anticancer properties. Overall, phenyl phenylacetate is a versatile compound that has a range of potential applications in various industries and research fields.

InChI:InChI=1/C14H12O2/c15-14(11-12-7-3-1-4-8-12)16-13-9-5-2-6-10-13/h1-10H,11H2

Upstream product

• 100914-90-7 α-phenoxy-cinnamic acid 
• 103-80-0 phenylacetyl chloride 
• 108-95-2 phenol 
• 103-82-2 phenylacetic acid 
• 1555-80-2 phenylacetic anhydride 
• 3282-32-4 2-diazo-acetophenone 
• 118-55-8 phenyl Salicylate 
• 77331-18-1 C₂₁H₂₀ClN₂O₉P*C₅H₅N 
• 201230-82-2 carbon monoxide 
• 100-51-6 benzyl alcohol 
• 7732-18-5 water 
• 101-41-7 benzeneacetic acid methyl ester 
• 100-39-0 benzyl bromide 
• 1864-94-4 phenyl formate 

Downstream Products

• 103-71-9 phenyl isocyanate 
• 108-95-2 phenol 
• 1786-05-6 4-hydroxy-3-phenylcoumarin 
• 114832-89-2 2-Phenylacetoxy-benzoic acid phenyl ester 
• 114832-91-6 6-[1-Phenyl-meth-(Z)-ylidene]-6H-5,12-dioxa-chrysen-11-one 
• 85531-17-5 tri-salicylic acid 
• 114832-92-7 C₂₇H₁₈O₇ 
• 2491-32-9 1-(4-Hydroxyphenyl)-2-phenylethanone 
• 2491-31-8 2-hydroxy-deoxybenzoin 
• 103-29-7 1,1'-(1,2-ethanediyl)bisbenzene 
• 108-88-3 toluene 
• 103-30-0 (E)-1,2-diphenyl-ethene 
• 3246-80-8 9-phenyl-9H-xanthene 
• 101-53-1 p-benzylphenol 

Relevant articles and documents

A solvent-reagent selection guide for Steglich-type esterification of carboxylic acids

The Steglich esterification is a widely employed method for the formation of esters under mild conditions. A number of issues regarding the sustainability of this transformation have been identified, chiefly the use of hazardous carbodiimide coupling reagents in conjunction with solvents with considerable issues such as dichloromethane (DCM) and N,N-dimethylformamide (DMF). To overcome these issues, we have developed a solvent-reagent selection guide for the formation of esters via Steglich-type reactions with the aim of providing safer, more sustainable conditions. Optimum reaction conditions have been identified after high-throughput screening of solvent-reagent combinations, namely the use of Mukaiyama's reagent (Muk) in conjunction with solvent dimethyl carbonate (DMC). The new reaction conditions were also exemplified through the synthesis of a small selection of building-block like molecules and includes the formation of t-butyl esters.

STRIGOLACTONE ANALOGS AND METHODS OF USING

Disclosed herein are compounds of Formula I and methods for regulating plant growth and/or combating root parasitic plants. Formulations containing one or more disclosed compounds or salts thereof, and one or more excipients are disclosed. Methods for reg

Rhodium-Catalyzed Carbonylative Coupling of Alkyl Halides with Phenols under Low CO Pressure

A rhodium-catalyzed carbonylative transformation of alkyl halides under low pressure of CO has been developed. This robust catalyst system allows using phenols as the carbonylative coupling partner and, meanwhile, exhibits high functional group tolerance and good chemoselectivity. Substrates even with a large steric hindrance group or multiple reaction sites can be selectively converted into the desired products in good to excellent yields. A gram-scale experiment was performed and delivered an almost quantitative amount of the product. Control experiments were performed as well, and a possible reaction mechanism is proposed.