macakurzin C

Base Information

Chemical Name:macakurzin C
CAS No.:42193-89-5
Molecular Formula:C₂₀H₁₆O₅
Molecular Weight:336.344
Hs Code.:

Synonyms:macakurzin C

Suppliers and Price of macakurzin C

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of macakurzin C

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of macakurzin C

There total 8 articles about macakurzin C 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: 83.0%

: C₂₇H₂₂O₅

: 42193-89-5
macakurzin C

Guidance literature:: With boron trichloride; In n-heptane; dichloromethane; at 0 - 20 ℃; for 2h;
DOI:10.1055/s-0034-1378904

Reference yield:

: C₂₉H₂₀O₆

: 42193-89-5
macakurzin C

Guidance literature:: Multi-step reaction with 3 steps

1: 1,8-diazabicyclo[5.4.0]undec-7-ene; copper(l) chloride / acetonitrile / 14 h / 0 °C

2: N,N-diethylaniline / 1 h / 270 °C

3: boron trichloride / dichloromethane; n-heptane / 2 h / 0 - 20 °C

With boron trichloride; 1,8-diazabicyclo[5.4.0]undec-7-ene; N,N-diethylaniline; copper(l) chloride; In n-heptane; dichloromethane; acetonitrile; 2: |Claisen Rearrangement;
DOI:10.1055/s-0034-1378904

Reference yield:

: 1616279-97-0
3-(benzyloxy)-5,7-dihydroxy-2-phenyl-4H-chromen-4-one

: 42193-89-5
macakurzin C

Guidance literature:: Multi-step reaction with 4 steps

1.1: pyridinium p-toluenesulfonate / dichloromethane / 10 h / 20 °C

2.1: 1,8-diazabicyclo[5.4.0]undec-7-ene / acetonitrile / 0.5 h / 20 °C

2.2: 16 h / 0 °C

3.1: N,N-diethylaniline / 1 h / 270 °C

4.1: boron trichloride / dichloromethane; n-heptane / 2 h / 0 - 20 °C

With pyridinium p-toluenesulfonate; boron trichloride; 1,8-diazabicyclo[5.4.0]undec-7-ene; N,N-diethylaniline; In n-heptane; dichloromethane; acetonitrile; 3.1: |Claisen Rearrangement;
DOI:10.1055/s-0034-1378904