1,3,5-Trihydroxy-2,4-bis(3-methyl-2-butenyl)-9(10H)-acridinone

Base Information

Chemical Name:1,3,5-Trihydroxy-2,4-bis(3-methyl-2-butenyl)-9(10H)-acridinone
CAS No.:28233-34-3
Molecular Formula:C24H27NO4
Molecular Weight:393.47500
Hs Code.:
Mol file:28233-34-3.mol

Synonyms:N-Methylatalaphyllin;N-methylatalphylline;n-methylataphylline;1,3,5-Trihydroxy-10-methyl-2,4-bis-(3-methyl-but-2-enyl)-10H-acridin-9-one;

Suppliers and Price of 1,3,5-Trihydroxy-2,4-bis(3-methyl-2-butenyl)-9(10H)-acridinone

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 4 raw suppliers

Chemical Property of 1,3,5-Trihydroxy-2,4-bis(3-methyl-2-butenyl)-9(10H)-acridinone

Chemical Property:

PSA：82.69000
LogP:4.82590

Purity/Quality:: 98% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of 1,3,5-Trihydroxy-2,4-bis(3-methyl-2-butenyl)-9(10H)-acridinone

There total 8 articles about 1,3,5-Trihydroxy-2,4-bis(3-methyl-2-butenyl)-9(10H)-acridinone 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:

: 108937-60-6
3,5-Dibenzyloxy-1-hydroxy-2,4-bis(3,3-dimethylallyl)-N-methylacridone

: 28233-34-3
N-methylatalaphylline

Guidance literature:: With sodium ethanolate; palladium on activated charcoal; In ethanol; for 0.666667h; Heating;

Reference yield:

: 63110-81-6
1,3-dihydroxy-5-methoxy-9(10H)-acridinone

: 28233-34-3
N-methylatalaphylline

Guidance literature:: Multi-step reaction with 7 steps

1: 900 mg / methanol; diethyl ether / 12 h / 0 °C

2: 10 mg / conc. H₂SO₄ / 12 h

3: 4 g / NaHCO₃, NaI / acetone / 18 h / Heating

4: 200 mg / BF₃ etherate / dioxane / 2 h

5: 50 mg / NaI, K₂CO₃ / acetone / 6 h / Heating

6: 25 mg / K₂CO₃ / acetone / 12 h / Heating

7: 6 mg / NaOEt / 10percent Pd-C / ethanol / 0.67 h / Heating

With sulfuric acid; boron trifluoride diethyl etherate; sodium ethanolate; sodium hydrogencarbonate; potassium carbonate; sodium iodide; palladium on activated charcoal; In 1,4-dioxane; methanol; diethyl ether; ethanol; acetone;

Reference yield:

: 115-18-4
2-methyl-3-buten-2-ol

: 28233-34-3
N-methylatalaphylline

Guidance literature:: Multi-step reaction with 4 steps

1: 200 mg / BF₃ etherate / dioxane / 2 h

2: 50 mg / NaI, K₂CO₃ / acetone / 6 h / Heating

3: 25 mg / K₂CO₃ / acetone / 12 h / Heating

4: 6 mg / NaOEt / 10percent Pd-C / ethanol / 0.67 h / Heating

With boron trifluoride diethyl etherate; sodium ethanolate; potassium carbonate; sodium iodide; palladium on activated charcoal; In 1,4-dioxane; ethanol; acetone;