531512-26-2

Basic information

• Product Name: urolithin M7
• CAS NO: 531512-26-2
• Molecular Weight: 244.204
• Mol File: 531512-26-2.mol

Chemical Properties

• Melting Point: >300 °C
• Boiling Point: 583.0±29.0 °C(Predicted)
• Density: 1.640±0.06 g/cm3(Predicted)
• CAS DataBase Reference: urolithin M7(CAS DataBase Reference)
• NIST Chemistry Reference: urolithin M7(531512-26-2)
• EPA Substance Registry System: urolithin M7(531512-26-2)

Safety Data

• Hazardous Substances Data: 531512-26-2(Hazardous Substances Data)

Usage

Uses

Urolithin M7 is an intestinal microbial metabolite of ellagitannins.

Upstream product

• 673-22-3 2-Hydroxy-4-methoxybenzaldehyde 
• 1346113-23-2 C₁₇H₁₄O₆ 
• 1346113-30-1 3,10-dimethoxy-6H-dibenzo[b,d]pyran-6-one-8-carboxylic acid 
• 1346113-31-2 8-acetyl-3,10-dimethoxy-6H-dibenzo[b,d]pyran-6-one 
• 1346113-32-3 8-acetoxy-3,10-dimethoxy-6H-dibenzo[b,d]pyran-6-one 
• 1346113-24-3 methyl (E)-3-(7-methoxy-2-oxo-2H-chromen-3-yl)acrylate 
• 696-62-8 para-iodoanisole 
• 1132-21-4 3,5-dimethoxybenzoic acid 

Relevant articles and documents

Palladium-Catalyzed, N-(2-Aminophenyl)acetamide-Assisted Ortho-Arylation of Substituted Benzamides: Application to the Synthesis of Urolithins B, M6, and M7

Pd-catalyzed, selective, monoarylation of ortho-C-H bonds of various benzamides with aryl/heteroaryl iodides has been realized using N-(2-aminophenyl)acetamide (APA) as a new bidentate directing group for the first time. The reaction was tolerant of a wid

An inverse electron-demand diels-alder-based total synthesis of urolithin M7

Urolithin M7 was synthesized from 2-hydroxy-4-methoxybenzaldehyde in 8 steps and 48% overall yield. The key step was an inverse electron demand Diels-Alder (IEDDA) reaction between diene 10 and the enamine (7) derived from dimethoxyacetaldehyde and pyrrolidine, which generated the 6H-dibenzo[b,d]pyran- 6-one skeleton. Georg Thieme Verlag Stuttgart - New York.