7702-17-2

Basic information

• Product Name: 4-(acetyloxy)-2,6-dimethoxyphenyl acetate
• Synonyms: 4-(acetyloxy)-2,6-dimethoxyphenyl acetate
• CAS NO: 7702-17-2
• Molecular Formula: C₁₂H₁₄O₆
• Molecular Weight: 254.23596
• Mol File: 7702-17-2.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 320.2°C at 760 mmHg
• Flash Point: 138.2°C
• Appearance: /
• Density: 1.195g/cm³
• Vapor Pressure: 0.000323mmHg at 25°C
• Refractive Index: 1.497
• CAS DataBase Reference: 4-(acetyloxy)-2,6-dimethoxyphenyl acetate(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(acetyloxy)-2,6-dimethoxyphenyl acetate(7702-17-2)
• EPA Substance Registry System: 4-(acetyloxy)-2,6-dimethoxyphenyl acetate(7702-17-2)

Safety Data

• Hazardous Substances Data: 7702-17-2(Hazardous Substances Data)

Usage

InChI:InChI=1/C12H14O6/c1-7(13)17-9-5-10(15-3)12(18-8(2)14)11(6-9)16-4/h5-6H,1-4H3

Upstream product

• 530-55-2 2,6-dimethoxy-p-quinone 
• 108-24-7 acetic anhydride 
• 29137-73-3 (1-Hydroxy-2,6-dimethoxy-4-oxo-cyclohexa-2,5-dienyl)-methoxy-acetic acid ethyl ester 
• 15233-65-5 2,6-dimethoxy-1,4-hydroquinone 
• 75-36-5 acetyl chloride 
• 134-96-3 syringic aldehyde 

Downstream Products

• 129168-54-3 3-Acetoxy-6-hydroxy-2,2',4,5'-tetramethoxybenzophenon 
• 129168-55-4 2,6-bis-(2,5-Dimethoxybenzoyl)-4-acetoxy-3,5-dimethoxyphenol 
• 21919-63-1 3-acetyl-4-hydroxy-2,6-dimethoxyphenyl acetate 
• 10176-68-8 4-hydroxy-2,6-dimethoxy-3-(3-(4-methoxyphenyl)-3-oxopropanoyl)phenyl 4-methoxybenzoate 
• 1456771-00-8 C₂₆H₁₈F₆O₇ 
• 1456770-99-2 C₂₆H₁₈F₆O₉ 
• 10176-70-2 5,7-dimethoxy-2-(4-methoxyphenyl)-4-oxo-4H-chromen-6-yl 4-methoxybenzoate 
• 6938-19-8 6-hydroxy-5,7-dimethoxy-2-(4-methoxyphenyl)-4H-chromen-4-one 
• 1456770-98-1 C₁₈H₁₃F₃O₅ 
• 1456770-97-0 C₁₈H₁₃F₃O₆ 
• 10176-71-3 ladanein 
• 1456770-96-9 BJ₇₅₁/1 
• 1456770-95-8 BJ₇₅₅-3 I 
• 1456770-94-7 C₁₈H₁₄O₆ 

Relevant articles and documents

A practical and economical high-yielding, six-step sequence synthesis of a flavone: Application to the multigram-scale synthesis of ladanein

Herein we report a short and economic synthesis of the antiviral flavonoid lead ladanein (1). Ladanein is obtained from 2,6-dimethoxyquinone (11) in six steps with 51% overall yield. After a high-yielding reductive acetylation and Fries rearrangement, the

Flavone derivatives and their use

The present invention relates to flavone derivatives and to compositions containing one or more of these flavone derivatives. The present invention further relates to flavone derivatives or compositions for use in the treatment and/or prevention of a vira

A note on the occurrence of 2, 6-dimethoxybenzoquinone in Rauwolfia vomitoria.

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