7-Isopentenyloxy-gamma-fagarine

Base Information

• Chemical Name: 7-Isopentenyloxy-gamma-fagarine
• CAS No.: 23417-92-7
• Molecular Formula: C₁₈H₁₉NO₄
• Molecular Weight: 313.353
• Hs Code.: 2934999090
• Mol file: 23417-92-7.mol

Synonyms:Furo[2,3-b]quinoline,4,8-dimethoxy-7-[(3-methyl-2-butenyl)oxy]- (8CI,9CI); 7-(Isopentenyloxy)-g-fagarine; 7-Isopenthyloxy-g-fagarine; 7-O-Isopentenyl-g-fagarine

Chemical Property of 7-Isopentenyloxy-gamma-fagarine

Chemical Property:

• PSA: 53.72000
• LogP: 4.34320

Purity/Quality:

98%min ^*data from raw suppliers

7-Prenyloxy-γ-Fagarine 95+% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

Technology Process of 7-Isopentenyloxy-gamma-fagarine

There total 5 articles about 7-Isopentenyloxy-gamma-fagarine 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: 85.0%

4,8-Dimethoxy-furo[2,3-b]quinolin-7-ol (5876-17-5,1363-10-6) + 3,3-dimethyl-allyl chloride (503-60-6) → 7-isopentenyloxy-γ-fagarine (23417-92-7)

Guidance literature:

With potassium carbonate;

DOI:10.1039/b506944k

Reference yield:

(7S,8R)-4-methoxy-7,8-dihydrofuro[2,3-b]quinoline-7,8-diol (865878-14-4) → 7-isopentenyloxy-γ-fagarine (23417-92-7)

Guidance literature:

Multi-step reaction with 3 steps

1: E_. coli nar B naphthalene cis-diol dehydrogenase

2: 85 percent / K₂CO₃

With E_. coli nar B naphthalene cis-diol dehydrogenase; potassium carbonate;

DOI:10.1039/b506944k

Reference yield:

4-chloro-7,8-dimethoxy-furo[2,3-b]quinoline (865878-27-9) → 7-isopentenyloxy-γ-fagarine (23417-92-7)

Guidance literature:

Multi-step reaction with 4 steps

1: 85 percent / BBr₃

2: 85 percent / K₂CO₃

With boron tribromide; potassium carbonate;

DOI:10.1039/b506944k

upstream raw materials:

4,8-Dimethoxy-furo[2,3-b]quinolin-7-ol

3,3-dimethyl-allyl chloride

(7S,8R)-4-methoxy-7,8-dihydrofuro[2,3-b]quinoline-7,8-diol

4-chloro-7,8-dimethoxy-furo[2,3-b]quinoline

Refernces