14882-94-1

Basic information

• Product Name: rutamarin
• Synonyms: rutamarin;2-(6-(2-methylbut-3-en-2-yl)-7-oxo-3,7-dihydro-2H-furo[3,2-g]chromen-2-yl)propan-2-yl acetate;2-(1-Acetoxy-1-methylethyl)-6-(1,1-dimethyl-2-propenyl)-2,3-dihydro-7H-furo[3,2-g][1]benzopyran-7-one;C09308
• CAS NO: 14882-94-1
• Molecular Formula: C₂₁H₂₄O₅
• Molecular Weight: 0
• Mol File: 14882-94-1.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 471.1°Cat760mmHg
• Flash Point: 204.9°C
• Appearance: /
• Density: 1.19g/cm³
• Vapor Pressure: 4.79E-09mmHg at 25°C
• Refractive Index: 1.555
• CAS DataBase Reference: rutamarin(CAS DataBase Reference)
• NIST Chemistry Reference: rutamarin(14882-94-1)
• EPA Substance Registry System: rutamarin(14882-94-1)

Safety Data

• Hazardous Substances Data: 14882-94-1(Hazardous Substances Data)

Usage

General Description

Rutamarin is a natural chemical compound found in several plants, including Ruta graveolens (common rue) and Citrus plants. It belongs to the class of compounds known as flavonoids, which are known for their antioxidant and anti-inflammatory properties. Rutamarin has been studied for its potential health benefits, including its anti-cancer, anti-inflammatory, and anti-viral properties. It has also been investigated for its potential use in the treatment of various diseases, including cancer, diabetes, and neurodegenerative disorders. Additionally, rutamarin has shown promise in promoting cardiovascular health and reducing the risk of stroke. Overall, rutamarin is a bioactive compound with potential therapeutic applications in various health conditions.

InChI:InChI=1/C21H24O5/c1-7-20(3,4)15-9-13-8-14-10-18(21(5,6)26-12(2)22)24-16(14)11-17(13)25-19(15)23/h7-9,11,18H,1,10H2,2-6H3/t18-/m0/s1

Upstream product

• 13164-04-0 2,3-dihydro-2-(2-hydroxypropan-2-yl)-6-(2-methylbut-3-en-2-yl)furo[3,2-g]chromen-7-one 
• 108-24-7 acetic anhydride 
• 1111-97-3 3-chloro-3-methylbut-1-yne 
• 65763-00-0 7-hydroxy-8-iodocoumarin 
• 21316-80-3 7-hydroxy-6-(3-methylbut-2-enyl)-3-(2-methylbut-3-en-2-yl)-2H-chromen-2-one 
• 93-35-6 7-hydroxy-2H-chromen-2-one 
• 1242260-99-6 4-benzyloxy-2-(3-methylbut-2-enyloxy)benzaldehyde 
• 1242261-00-2 C₂₇H₃₄O₅ 
• 1242261-01-3 7-benzyloxy-6-(3-methylbut-2-enyl)-3-(2-methylbut-3-en-2-yl)-2H-chromen-2-one 
• 95-01-2 2,4-Dihydroxybenzaldehyde 
• 52085-14-0 4-benzoxy-salicylaldehyde 
• 112699-35-1 8-iododemethylsuberosin acetate 
• 112723-61-2 6-(3',3'-dimethylallyl)-7-(3'',3''-dimethylallyloxy)-8-iodocoumarin 
• 112699-37-3 8-iododemethylsuberosin 

Relevant articles and documents

Improved total synthesis of racemic rutamarin

An improved, convenient and cost-effective process, using 2,4-dihydroxybenzaldehyde 2 as starting material for (±)-rutamarin 1, is described. The overall yield of 1 is 44% in eight steps, requiring no chromatographic purification. The Japan Institute of Heterocyclic Chemistry.