4861-85-2

Usage

Uses

Used in Fragrance Industry:
ISOPROPYL PHENYLACETATE is used as a fragrance ingredient for its fragrant, rose-like scent. It is valued for its ability to add a sweet, honey-like aroma with a wine undertone to various products, enhancing their overall sensory appeal.
Used in Flavor Industry:
ISOPROPYL PHENYLACETATE is used as a flavoring agent for its sweet, honey-like taste with a wine undertone. It is commonly utilized in the creation of flavors for the food and beverage industry, providing a unique and pleasant taste experience.
Used in Cosmetics and Personal Care Industry:
ISOPROPYL PHENYLACETATE is used as a component in cosmetics and personal care products for its pleasant scent and flavor. It can be found in perfumes, lotions, and other products to provide a desirable sensory experience for the user.
Used in the Pharmaceutical Industry:
ISOPROPYL PHENYLACETATE may be used in the pharmaceutical industry as a flavoring agent for medications, making them more palatable and improving patient compliance. Its sweet, honey-like taste can help mask the bitterness of certain drugs, making them more acceptable for consumption.

Air & Water Reactions

Insoluble in water.

Reactivity Profile

ISOPROPYL PHENYLACETATE is an ester. Esters react with acids to liberate heat along with alcohols and acids. Strong oxidizing acids may cause a vigorous reaction that is sufficiently exothermic to ignite the reaction products. Heat is also generated by the interaction of esters with caustic solutions. Flammable hydrogen is generated by mixing esters with alkali metals and hydrides.

Health Hazard

ACUTE/CHRONIC HAZARDS: ISOPROPYL PHENYLACETATE does not present a serious hazard in normal use. However, it should be borne in mind that the toxicological and physiological properties are not yet well defined.

Fire Hazard

ISOPROPYL PHENYLACETATE is combustible.

InChI:InChI=1/C11H14O2/c1-9(2)13-11(12)8-10-6-4-3-5-7-10/h3-7,9H,8H2,1-2H3

Upstream product

• 103-82-2 phenylacetic acid 
• 75178-11-9 Phenyl-acetic acid [2,2']bipyridinyl-6-yl ester 
• 67-63-0 isopropyl alcohol 
• 101-41-7 benzeneacetic acid methyl ester 
• 38042-52-3 2-chloro-2-(phenylsulfinyl)-1-phenyl-1-ethanone 
• 630-20-6 1,1,1,2-tetrachoroethane 
• 7637-07-2 boron trifluoride 
• 98-59-9 p-toluenesulfonyl chloride 
• 109853-53-4 3-(2-phenylacetyl)-1,3-oxazolidin-2-one 
• 103-81-1 Benzeneacetamide 
• 50707-41-0 C₁₀H₁₅N₃ 
• 201230-82-2 carbon monoxide 
• 27992-27-4 sodium 2-benzylidene-1-tosylhydrazin-1-ide 
• 1576-35-8 toluene-4-sulfonic acid hydrazide 

Downstream Products

• 130786-15-1 isopropyl (2S,3R)-3-hydroxy-2-phenylhexanoate 
• 7500-45-0 N-benzylphenylacetamide 

Relevant academic research and scientific papers

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.

Photoinduced Diverse Reactivity of Diazo Compounds with Nitrosoarenes

A diverse reactivity of diazo compounds with nitrosoarene in an oxygen-transfer process and a formal [2 + 2] cycloaddition is reported. Nitosoarene has been exploited as a mild oxygen source to oxidize an in situ generated carbene intermediate under visible-light irradiation. UV-light-mediated in situ generated ketenes react with nitosoarenes to deliver oxazetidine derivatives. These operationally simple processes exemplify a transition-metal-free and catalyst-free protocol to give structurally diverse α-ketoesters or oxazetidines.

Room Temperature Coupling of Aryldiazoacetates with Boronic Acids Enhanced by Blue Light Irradiation

A visible-light-promoted photochemical protocol is reported for the coupling of aryldiazoacetates with boronic acids. This photochemical reaction shows great enhancement compared to the same protocol performed in the absence of light. Except for a few cases, the room temperature coupling in the dark (thermal process) generally does not work. When it does, it is likely to also involve free carbenes as key intermediates. Alternatively, photochemical reactions show a broad scope, can be performed under air and tolerate a wide variety of functional groups. Reaction-evolution monitoring, DFT calculations and control experiments have been used to evaluate the main aspects of this intricate mechanistic scenario. Biologically active molecules Adiphenine, Benactyzine and Aprophen have been prepared as examples of synthetic applications.

PHOSPHINIC AMIDE PRODRUGS OF TENOFOVIR

Compounds of Formula I: I and their pharmaceutically acceptable salts are useful for the inhibition of HIV reverse transcriptase. The compounds may also be useful for the prophylaxis or treatment of infection by HIV and in the prophylaxis, delay in the onset or progression, and treatment of AIDS. The compounds and their salts can be employed as ingredients in pharmaceutical compositions, optionally in combination with other antiviral agents, immunomodulators, antibiotics or vaccines.

Preparation of Organic Nitrates from Aryldiazoacetates and Fe(NO3)3·9H2O

A thermal protocol is reported for the formal insertion of nitric acid into aryldiazoacetates using Fe(NO3)3·9H2O. This strategy is mild and high yielding and allows the preparation of a large variety of members of an unprecedented family of organic nitrates. The nitrate group can be also readily transformed into other functional groups and heterocyclic moieties and can possibly allow new biological explorations of untapped potential associated with their NO-releasing ability.

[Co(MeTAA)] Metalloradical Catalytic Route to Ketenes via Carbonylation of Carbene Radicals

An efficient synthetic strategy towards beta-lactams, amides, and esters involving “in situ” generation of ketenes and subsequent trapping with nucleophiles is presented. Carbonylation of carbene radical intermediates using the cheap and highly active cobalt(II) tetramethyltetraaza[14]annulene catalyst [Co(MeTAA)] provides a convenient one-pot synthetic protocol towards substituted ketenes. N-tosylhydrazones are used as carbene precursors, thereby bridging the gap between aldehydes and ketenes. Activation of these carbene precursors by the metalloradical cobalt(II) catalyst affords CoIII-carbene radicals, which subsequently react with carbon monoxide to form ketenes. In the presence of a nucleophile (imine, alcohol, or amine) in the reaction medium the ketene is immediately trapped, resulting in the desired products in a one-pot synthetic protocol. The β-lactams formed upon reaction with imines are produced in a highly trans-selective manner.

Ni-Catalyzed chemoselective alcoholysis of: N -acyloxazolidinones

Although N-acyloxazolidinone-based (catalytic) asymmetric synthetic methodologies occupy an important position in modern organic synthesis, the catalytic cleavage of a chiral auxiliary remains underdeveloped. We report the Ni(cod)2/bipyr.-catalyzed alcoholysis of N-acyloxazolidinones to deliver esters. The reaction is broad in scope for both N-acyloxazolidinone substrates and alcohol nucleophiles, and displays good functional group tolerance and excellent chemoselectivity. A gram-scale methanolysis allowed the enantioselective synthesis of the C22-C26 segment of a close analogue of the potent immunosuppressant agent FK506.

Carbon monoxide is used as a source of halogen compound heterogeneous palladium catalyst in the presence of the aldehyde carbonyl compound by reaction carbonylation method (by machine translation)

[Problem] catalyst and the presence of carbon monoxide, the halogen compound is a carbonyl compound in the carbonylation reaction, catalysts or carbon monoxide source technique has problems. [Solution] the presence of the catalyst and the carbon monoxide, the halogen compound is carbonylation reaction method for producing a carbonyl compound, As a heterogeneous palladium catalyst, carbon monoxide is produced from an aldehyde carbonyl compound used in the method. [Drawing] no (by machine translation)

Synthesis and characterization of stable ZnO nanoparticles using imidazolium-based ionic liquids and their applications in esterification reaction

ZnO nanoparticles have been synthesized from zinc acetate using 1-octyl-3-methylimidazolium hexafluorophosphate as capping agent under microwave irradiation condition in a very short period of time and characterized using UV-visible spectroscopy, powder X-ray diffraction, scanning electron microscopy, transmission electron microscopy and NH3-TPD analysis. The ZnO NPs have been used as a solid reusable acid catalyst for esterification of carboxylic acids with alcohols.

LED lighting as a simple, inexpensive, and sustainable alternative for Wolff rearrangements

The Wolff rearrangement is one of the best methods for chain homologation. However, it still suffers from many drawbacks with respect to its practical execution in the laboratory. We wish to demonstrate the use of commercial LED lamps as a sustainable alternative for the classic experimental protocols typically used for Wolff rearrangements. This journal is