moracin I

Base Information

Chemical Name:moracin I
CAS No.:73338-88-2
Molecular Formula:C20H20O4
Molecular Weight:324.3704
Hs Code.:
DSSTox Substance ID:DTXSID30223568
Nikkaji Number:J1.454.356B
Wikidata:Q83102023
Metabolomics Workbench ID:45980
ChEMBL ID:CHEMBL463435

Synonyms:moracin I;6-Benzofuranol, 2-(5-hydroxy-3-methoxy-2-(3-methyl-2-butenyl)phenyl)-;73338-88-2;CHEMBL463435;SCHEMBL6823496;DTXSID30223568;6-Hydroxy-2-(5-hydroxy-3-methoxy-2-prenylphenyl)benzofuran;2-[5-hydroxy-3-methoxy-2-(3-methylbut-2-en-1-yl)phenyl]-1-benzofuran-6-ol

Suppliers and Price of moracin I

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
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Total 0 raw suppliers

Chemical Property of moracin I

Chemical Property:

Vapor Pressure:3.88E-08mmHg at 25°C
Boiling Point:433.9°Cat760mmHg
Flash Point:216.2°C
Density:1.209g/cm³
XLogP3:5.2
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:4
Exact Mass:324.13615911
Heavy Atom Count:24
Complexity:445

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(=CCC1=C(C=C(C=C1OC)O)C2=CC3=C(O2)C=C(C=C3)O)C

Technology Process of moracin I

There total 5 articles about moracin I 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: 96.0%

: 138038-90-1
2-<3-t-butyldimethylsilyloxy-5-methoxy-2-(3-methylbut-2-enyl)phenyl>-6-t-butyldiphenylsilyloxybenzofuran

: 73338-88-2
moracin I

Guidance literature:: With tetrabutyl ammonium fluoride; In tetrahydrofuran; Ambient temperature;
DOI:10.1016/S0040-4020(01)81952-9

Reference yield:

: 96700-91-3
3,5-dimethoxyphenol tert-butyldimethylsilyl ether

: 73338-88-2
moracin I

Guidance literature:: Multi-step reaction with 5 steps

1: 1) BuLi, 2) CuBrSMe₂ / 1) THF, ether, rt, 3 h, 2a) 0 deg C, 1 h, b) 2 h, 0 deg C

2: 50 percent / BuLi, diphenylphosphine / tetrahydrofuran / Heating

3: 96 percent / pyridine / 16 h / Ambient temperature

5: 96 percent / Bu₄NF / tetrahydrofuran / Ambient temperature

With pyridine; n-butyllithium; copper(I) bromide dimethylsulfide complex; tetrabutyl ammonium fluoride; diphenylphosphane; In tetrahydrofuran;
DOI:10.1016/S0040-4020(01)81952-9

Reference yield:

: 138038-87-6
1-t-butyldimethylsilyloxy-3-hydroxy-5-methoxy-4-(3-methylbut-2-enyl)benzene

: 73338-88-2
moracin I

Guidance literature:: Multi-step reaction with 3 steps

1: 96 percent / pyridine / 16 h / Ambient temperature

3: 96 percent / Bu₄NF / tetrahydrofuran / Ambient temperature

With pyridine; tetrabutyl ammonium fluoride; In tetrahydrofuran;
DOI:10.1016/S0040-4020(01)81952-9