71989-95-2

Basic information

• Product Name: 4-FORMYL-2-METHOXYPHENYL 3,4,5-TRIMETHOXYBENZOATE
• Synonyms: 4-FORMYL-2-METHOXYPHENYL 3,4,5-TRIMETHOXYBENZOATE;3,4,5-Trimethoxybenzoic acid 4-formyl-2-methoxyphenyl ester
• CAS NO: 71989-95-2
• Molecular Formula: C₁₈H₁₈O₇
• Molecular Weight: 346.33
• EINECS: 276-269-5
• Mol File: 71989-95-2.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 481.1°C at 760 mmHg
• Flash Point: 211.8°C
• Appearance: /
• Density: 1.234g/cm³
• Vapor Pressure: 2.05E-09mmHg at 25°C
• Refractive Index: 1.564
• CAS DataBase Reference: 4-FORMYL-2-METHOXYPHENYL 3,4,5-TRIMETHOXYBENZOATE(CAS DataBase Reference)
• NIST Chemistry Reference: 4-FORMYL-2-METHOXYPHENYL 3,4,5-TRIMETHOXYBENZOATE(71989-95-2)
• EPA Substance Registry System: 4-FORMYL-2-METHOXYPHENYL 3,4,5-TRIMETHOXYBENZOATE(71989-95-2)

Safety Data

• Hazardous Substances Data: 71989-95-2(Hazardous Substances Data)

Usage

General Description

4-FORMYL-2-METHOXYPHENYL 3,4,5-TRIMETHOXYBENZOATE is a chemical compound with the molecular formula C21H22O10. It is a derivative of benzoic acid and contains three methoxy groups attached to the benzene ring, as well as a formyl and a methoxyphenyl group. 4-FORMYL-2-METHOXYPHENYL 3,4,5-TRIMETHOXYBENZOATE has potential applications in the field of chemistry and pharmaceuticals due to its unique structure and properties. Its precise uses and effects would depend on its specific applications and the context in which it is used.

InChI:InChI=1/C18H18O7/c1-21-14-7-11(10-19)5-6-13(14)25-18(20)12-8-15(22-2)17(24-4)16(9-12)23-3/h5-10H,1-4H3

Upstream product

• 118-41-2 Eudesmic acid 
• 4521-61-3 3,4,5-Trimethoxybenzoyl chloride 
• 121-33-5 vanillin 

Relevant articles and documents

Synthesis, evaluation, and molecular docking studies of cycloalkyl/aryl-3,4,5-trimethylgallates as potent non-ulcerogenic and gastroprotective anti-inflammatory agents

In our effort to identify the effective gastric sparing and protective anti-inflammatory agents, a series of cycloalkyl/aryl-3,4,5-trimethylgallates were synthesized and characterized. The physicochemical properties were studied to assess the lipophilicity and chemical stability. Subsequently, the compounds were evaluated for their anti-inflammatory activity and effect on gastric mucosa by most active compounds. All the compounds exhibited promising anti-inflammatory activity. In particular, 4a, 4b, 4g, and 4h emerged as the most active compounds in the series. The results of gastric mucosal studies and biochemical estimations suggested that these compounds are non-ulcerogenic and gastroprotective. The molecular docking analysis was performed to understand the binding interactions of these compounds to cyclooxygenase isoenzyme (COX-1 and COX-2). The results from this investigation suggests cycloalkyl/aryl-3,4,5- trimethylgallates as potent safer gastrosparing and protective anti-inflammatory agents.