2664-32-6

Basic information

• Product Name: 4-ISOPROPYLPHENYL ACETATE
• Synonyms: 4-ISOPROPYLPHENYL ACETATE;p-cumenyl acetate;4-Isopropylphenol acetate;Acetic acid 4-isopropylphenyl ester;Acetic acid p-isopropylphenyl ester;(4-propan-2-ylphenyl) acetate;(4-propan-2-ylphenyl) ethanoate;NSC 407857
• CAS NO: 2664-32-6
• Molecular Formula: C₁₁H₁₄O₂
• Molecular Weight: 178.23
• EINECS: 220-192-1
• Mol File: 2664-32-6.mol
• Article Data: 16

Chemical Properties

• Boiling Point: 241℃
• Flash Point: 93℃
• Appearance: /
• Density: 1.006
• Vapor Pressure: 0.0362mmHg at 25°C
• Refractive Index: 1.496
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 4-ISOPROPYLPHENYL ACETATE(CAS DataBase Reference)
• NIST Chemistry Reference: 4-ISOPROPYLPHENYL ACETATE(2664-32-6)
• EPA Substance Registry System: 4-ISOPROPYLPHENYL ACETATE(2664-32-6)

Safety Data

• Hazardous Substances Data: 2664-32-6(Hazardous Substances Data)

Usage

General Description

4-Isopropylphenyl acetate, also known as isopropylphenyl acetate or 4-acetoxy-1-isopropylbenzene, is a chemical compound with the molecular formula C11H14O2. It is commonly used as a fragrance agent and flavoring ingredient in various consumer products. It is a clear, colorless liquid with a sweet, floral scent and is often used in perfumes, cosmetics, and food products. 4-Isopropylphenyl acetate is also known for its anti-inflammatory properties and is used in some pharmaceutical products. It is typically synthesized through the reaction of isopropylphenol with acetic anhydride, and is considered to be relatively stable and non-toxic. Overall, 4-isopropylphenyl acetate is a versatile chemical with various industrial and commercial applications.

InChI:InChI=1/C11H14O2/c1-8(2)10-4-6-11(7-5-10)13-9(3)12/h4-8H,1-3H3

Upstream product

• 99-89-8 4-Isopropylphenol 
• 75-36-5 acetyl chloride 
• 645-13-6 4-isopropylacetophenone 
• 98-82-8 Isopropylbenzene 
• 64-19-7 acetic acid 
• 506-96-7 Acetyl bromide 
• 28530-42-9 benzyl 4-(isopropyl)phenyl ether 
• 108-24-7 acetic anhydride 
• 108-05-4 vinyl acetate 

Downstream Products

• 1205-91-0 benzene-1,4-diyl diacetate 
• 13031-43-1 4-acetyloxyacetophenone 
• 99-89-8 4-Isopropylphenol 
• 1634-36-2 1-(2-hydroxy-5-isopropylphenyl)ethanone 
• 49619-58-1 3-formyl-6-isopropylchromone 

Relevant articles and documents

Direct Acetoxylation of Arenes

Acetoxylation of arenes is an important reaction and an unmet need in chemistry. We report a metal-free, direct acetoxylation reaction using sodium nitrate under an anhydrous environment of trifluoroacetic acid, acetic acid, and acetic anhydride. Arenes (31 examples), with oxidation potentials (Eox, in V vs SCE) lower than benzene (2.48 V), were acetoxylated with good yields and regioselectivity. A stepwise, single electron-transfer mechanism is proposed.

2, 4-diaminopyrimidine compound containing phenol fragment, preparation method, pharmaceutical compositions and use thereof

The invention discloses a 2, 4-diaminopyrimidine compound containing phenol fragment with a general formula I shown in the specification, pharmaceutically acceptable salts or pharmaceutically acceptable solvates, a preparation method thereof, pharmaceutical compositions containing the compounds, and use of the compounds in preparation of drugs for preventing or treating anaplastic lymphoma kinaserelated abnormal cell proliferation, morphological changes, hyperkinesia and other associated diseases in organisms, and angiogenesis or cancerometastasis associated diseases, especially use in drugsfor treating or preventing tumor growth and metastasis.

Rice husk ash: A new, cheap, efficient, and reusable reagent for the protection of alcohols, phenols, amines, and thiols

Amild, efficient, and eco-friendly protocol for the protection of alcohols and phenols as trimethylsilyl ethers has been developed using rice husk ash as a reagent. This reagent is also able to catalyze the acetylation of alcohols, phenols, thiols, and amines with acetic anhydride. All reactions were performed under mild conditions in good to high yields. Copyright