27688-85-3

Basic information

• Product Name: [3,4-bis(phenylmethoxy)phenyl] acetate
• Synonyms: [3,4-bis(phenylmethoxy)phenyl] acetate
• CAS NO: 27688-85-3
• Molecular Formula: C₂₂H₂₀O₄
• Molecular Weight: 348.39
• Mol File: 27688-85-3.mol
• Article Data: 1

Chemical Properties

• Melting Point: 95-98 °C(Solv: methanol (67-56-1))
• Boiling Point: 496.2°Cat760mmHg
• Flash Point: 217°C
• Appearance: /
• Density: 1.175g/cm³
• Vapor Pressure: 5.52E-10mmHg at 25°C
• Refractive Index: 1.589
• CAS DataBase Reference: [3,4-bis(phenylmethoxy)phenyl] acetate(CAS DataBase Reference)
• NIST Chemistry Reference: [3,4-bis(phenylmethoxy)phenyl] acetate(27688-85-3)
• EPA Substance Registry System: [3,4-bis(phenylmethoxy)phenyl] acetate(27688-85-3)

Safety Data

• Hazardous Substances Data: 27688-85-3(Hazardous Substances Data)

Usage

Description

[3,4-bis(phenylmethoxy)phenyl] acetate is a chemical compound characterized by its unique structure, featuring a central phenyl ring with two phenylmethoxy groups attached and an acetate group connected to it. [3,4-bis(phenylmethoxy)phenyl] acetate is known for its potential applications across various industries, including pharmaceuticals, materials science, and organic chemistry, due to its distinctive chemical properties and versatility in synthesis.

Uses

Used in Pharmaceutical Industry:
[3,4-bis(phenylmethoxy)phenyl] acetate is used as a building block for the synthesis of various organic compounds, contributing to the development of new pharmaceutical products. Its unique chemical structure allows for the creation of innovative drugs with potential therapeutic benefits.
Used in Materials Science:
In the field of materials science, [3,4-bis(phenylmethoxy)phenyl] acetate is utilized as a starting material for the production of complex molecules and advanced materials. Its properties make it suitable for specific chemical reactions, enabling the development of novel materials with enhanced characteristics.
Used in Organic Chemistry:
[3,4-bis(phenylmethoxy)phenyl] acetate serves as an essential component in organic chemistry, where it is employed in the synthesis of a wide range of organic compounds. Its unique structure and reactivity make it a valuable asset in the development of new chemical products and processes.

InChI:InChI=1/C22H20O4/c1-17(23)26-20-12-13-21(24-15-18-8-4-2-5-9-18)22(14-20)25-16-19-10-6-3-7-11-19/h2-14H,15-16H2,1H3

Upstream product

• 27688-86-4 3,4-dibenzyloxyphenol 
• 75-36-5 acetyl chloride 
• 5447-02-9 3,4-dibenzyloxybenzaldehyde 
• 100-39-0 benzyl bromide 
• 139-85-5 3,4-dihydroxybenzaldehyde 

Downstream Products

• 627489-15-0 acetic acid 4,5-bis-benzyloxy-2-iodo-phenyl ester 
• 524-12-9 wedelolactone 
• 627489-05-8 2-(2,6-dihydroxy-4-methoxy-phenyl)-5,6-dihydroxy-benzofuran-3-carboxylic acid methyl ester 
• 344303-12-4 4,5-bis-benzyloxy-2-(2,6-bis-benzyloxy-4-methoxy-phenylethynyl)-phenol 
• 627489-61-6 acetic acid 4,5-bis-benzyloxy-2-(2,6-bis-benzyloxy-4-methoxy-phenylethynyl)-phenyl ester 
• 344303-15-7 5,6-bis-benzyloxy-2-(2,6-bis-benzyloxy-4-methoxy-phenyl)-benzofuran-3-carboxylic acid methyl ester 
• 27688-92-2 1-(3,4-bis(benzyloxy)phenoxy)-3-(isopropylamino)-2-propanol 
• 53562-78-0 OXY-Isoprenaline 

Relevant articles and documents

Total Synthesis of Wedelolactone

The total synthesis of wedelolactone, a naturally occurring direct inhibitor of IKK complex that can suppress LPS-induced caspase-11 expression, using a convergent synthetic approach, is described. The key steps involved in this synthesis include the palladium-catalyzed Sonogashira reaction and the palladium-catalyzed carbonylative annulation reaction. This approach allows access to diversified analogues of wedelolactone.