7H-Furo[3,2-g][1]benzopyran-7-one, 9-methoxy-4-(3-methyl-2-butenyl)-

Base Information

• Chemical Name: 7H-Furo[3,2-g][1]benzopyran-7-one, 9-methoxy-4-(3-methyl-2-butenyl)-
• CAS No.: 10523-54-3
• Molecular Formula: C17H16O4
• Molecular Weight: 284.30700
• DSSTox Substance ID: DTXSID101156269
• Nikkaji Number: J109.875F
• Mol file: 10523-54-3.mol

Synonyms:Alloimperatorin methyl ether;10523-54-3;9-methoxy-4-(3-methylbut-2-enyl)furo[3,2-g]chromen-7-one;7H-Furo[3,2-g][1]benzopyran-7-one, 9-methoxy-4-(3-methyl-2-butenyl)-;5-Benzofuranacrylic acid, 6-hydroxy-7-methoxy-4-(3-methyl-2-butenyl)-, .delta.-lactone;6-Hydroxy-7-methoxy-4-(3-methyl-2-butenyl)-5-benzofuranacrylic acid delta-lactone;Alloimperatorin methyl;Methyl ether of alloimperatorin;DTXSID101156269;9-Methoxy-4-(3-methyl-2-butenyl)-7H-furo[3,2-g]chromen-7-one #;9-Methoxy-4-(3-methyl-2-buten-1-yl)-7H-furo[3,2-g][1]benzopyran-7-one

Chemical Property of 7H-Furo[3,2-g][1]benzopyran-7-one, 9-methoxy-4-(3-methyl-2-butenyl)-

Chemical Property:

• Melting Point: 109 °C (ethanol)
• PSA: 52.58000
• LogP: 4.05650
• XLogP3: 3.9
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 3
• Exact Mass: 284.10485899
• Heavy Atom Count: 21
• Complexity: 463

Purity/Quality:

98%,99%, ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC(=CCC1=C2C=CC(=O)OC2=C(C3=C1C=CO3)OC)C

Technology Process of 7H-Furo[3,2-g][1]benzopyran-7-one, 9-methoxy-4-(3-methyl-2-butenyl)-

There total 5 articles about 7H-Furo[3,2-g][1]benzopyran-7-one, 9-methoxy-4-(3-methyl-2-butenyl)- which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

imperatorin (482-44-0) → Alloimperatorin methyl ether (10523-54-3)

Guidance literature:

Multi-step reaction with 2 steps

1: N,N-diethylaniline / 1 h / Heating

2: K₂CO₃ / acetone / 24 h / Heating

With potassium carbonate; N,N-diethylaniline; In acetone;

Reference yield:

Alloimperatorin (642-05-7) + methyl iodide (74-88-4) → Alloimperatorin methyl ether (10523-54-3)

Guidance literature:

With potassium carbonate; In acetone; for 24h; Heating;

Reference yield:

diazomethane (186581-53-3,908094-01-9,334-88-3) → Alloimperatorin methyl ether (10523-54-3)

Guidance literature:

With methanol;

upstream raw materials:

Alloimperatorin

methyl iodide

diazomethane

imperatorin