4-Methoxylonchocarpin

Base Information

Chemical Name:4-Methoxylonchocarpin
CAS No.:51589-67-4
Molecular Formula:C21H20O4
Molecular Weight:336.387
Hs Code.:
Nikkaji Number:J1.112.741J
Wikidata:Q76415720
Metabolomics Workbench ID:26555
ChEMBL ID:CHEMBL369768

Synonyms:4-methoxylonchocarpin;CHEMBL369768;4-Hydroxylonchocarpin methyl ether;51589-67-4;2-Propen-1-one, 1-(5-hydroxy-2,2-dimethyl-2H-1-benzopyran-6-yl)-3-(4-methoxyphenyl)-, (2E)-;SCHEMBL13534952;CHEBI:180251;BDBM50505207;HY-N11768;LMPK12120079;(E)-1-(5-hydroxy-2,2-dimethyl-chromen-6-yl)-3-(4-methoxyphenyl)prop-2-en-1-one;CS-0834514;(E)-1-(5-hydroxy-2,2-dimethylchromen-6-yl)-3-(4-methoxyphenyl)prop-2-en-1-one;1-(2,2-Dimethyl-5-hydroxy-2H-1-benzopyran-6-yl)-3-(4-methoxyphenyl)-2-propene-1-one

Suppliers and Price of 4-Methoxylonchocarpin

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
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price

Total 0 raw suppliers

Chemical Property of 4-Methoxylonchocarpin

Chemical Property:

XLogP3:4.8
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:4
Exact Mass:336.13615911
Heavy Atom Count:25
Complexity:528

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1(C=CC2=C(O1)C=CC(=C2O)C(=O)C=CC3=CC=C(C=C3)OC)C
Isomeric SMILES:CC1(C=CC2=C(O1)C=CC(=C2O)C(=O)/C=C/C3=CC=C(C=C3)OC)C

Technology Process of 4-Methoxylonchocarpin

There total 8 articles about 4-Methoxylonchocarpin 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: 77.0%

: 24672-84-2
6-acetyl-5-hydroxy-2,2-dimethylchromene

: 123-11-5
4-methoxy-benzaldehyde

: 51589-67-4
(E)-1-(5-hydroxy-2,2-dimethyl-2H-chromen-6-yl)-3-(4-methoxyphenyl)prop-2-en-1-one

Guidance literature:: With barium dihydroxide; In ethanol; for 6h; Heating;
DOI:10.1016/S0031-9422(02)00475-2

Reference yield: 68.0%

: 511530-03-3
1-(5-hydroxy-2,2-dimethyl-3,4-dihydro-2H-chromen-6-yl)-3-(4-methoxyphenyl)propan-1-one

: 51589-67-4
(E)-1-(5-hydroxy-2,2-dimethyl-2H-chromen-6-yl)-3-(4-methoxyphenyl)prop-2-en-1-one

Guidance literature:: With 2,3-dicyano-5,6-dichloro-p-benzoquinone; In benzene;
DOI:10.1016/j.bmcl.2004.05.071

Reference yield: 54.0%

: 637-69-4,24936-44-5
4-Methoxystyrene

: 54287-99-9
5-hydroxy-2,2-dimethyl-2H-chromene-6-carbaldehyde

: 51589-67-4
(E)-1-(5-hydroxy-2,2-dimethyl-2H-chromen-6-yl)-3-(4-methoxyphenyl)prop-2-en-1-one

Guidance literature:: With 1,2,3,4-tetraphenylcyclopentadiene; dichloro(pentamethylcyclopentadienyl)rhodium (III) dimer; copper diacetate; In 1,2-dichloro-ethane; at 120 ℃; for 18h; regioselective reaction; Inert atmosphere;
DOI:10.1002/anie.201203224