Artocarpin

Base Information

Chemical Name:Artocarpin
CAS No.:7608-44-8
Molecular Formula:C26H28O6
Molecular Weight:436.505
Hs Code.:
NSC Number:241010
Nikkaji Number:J94.466A
Wikidata:Q27133884
Metabolomics Workbench ID:44599
ChEMBL ID:CHEMBL72617
Mol file:7608-44-8.mol

Synonyms:artocarpin;artocarpin lectin

Suppliers and Price of Artocarpin

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

Medical Isotopes, Inc.
Artocarpin 95%
10 mg
$ 1400.00

Crysdot
Artocarpin 95+%
5mg
$ 730.00

Arctom
Artocarpin
5mg
$ 513.00

Total 20 raw suppliers

Chemical Property of Artocarpin

Chemical Property:

Boiling Point:667.1±55.0 °C(Predicted)
PKA:6.38±0.40(Predicted)
PSA：100.13000
Density:1.242±0.06 g/cm3(Predicted)
LogP:5.76330
XLogP3:5.7
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:6
Exact Mass:436.18858861
Heavy Atom Count:32
Complexity:762

Purity/Quality:

98% ^*data from raw suppliers

Artocarpin 95% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)C=CC1=C(C=C2C(=C1O)C(=O)C(=C(O2)C3=C(C=C(C=C3)O)O)CC=C(C)C)OC
Isomeric SMILES:CC(C)/C=C/C1=C(C=C2C(=C1O)C(=O)C(=C(O2)C3=C(C=C(C=C3)O)O)CC=C(C)C)OC

Technology Process of Artocarpin

There total 14 articles about Artocarpin 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: 60.0%

: 1443276-30-9
(E)-5-hydroxy-2-(4-hydroxy-2-((4-methoxybenzyl)oxy)phenyl)-7-methoxy-6-(3-methylbut-1-en-1-yl)-3-(3-methylbut-2-en-1-yl)-4H-chromen-4-one

: 7608-44-8
Artocarpin

Guidance literature:: With ethanethiol; tin(ll) chloride; In acetonitrile; at 20 ℃;
DOI:10.1016/j.tet.2013.05.024

Reference yield: 18.0%

: 1443276-31-0
(E)-5-hydroxy-7-methoxy-2-(2-methoxy-4-((4-methoxybenzyl)oxy)phenyl)-6-(3-methylbut-1-en-1-yl)-3-(3-methylbut-2-en-1-yl)-4H-chromen-4-one

: 1443276-28-5
(E)-5-hydroxy-2-(4-hydroxy-2-methoxyphenyl)-7-methoxy-6-(3-methylbut-1-en-1-yl)-3-(3-methylbut-2-en-1-yl)-4H-chromen-4-one

: 7608-44-8
Artocarpin

Guidance literature:: With n-butyllithium; ethanethiol; In N,N,N,N,N,N-hexamethylphosphoric triamide; at 0 - 70 ℃; for 2h; Inert atmosphere;
DOI:10.1016/j.tet.2013.05.024

Reference yield:

: 5916-10-9
(E)-2-(2,4-dimethoxyphenyl)-5-hydroxy-7-methoxy-6-(3-methylbut-1-en-1-yl)-3-(3-methylbut-2-en-1-yl)-4H-chromen-4-one

: 7608-44-8
Artocarpin

Guidance literature:: Multi-step reaction with 3 steps

1.1: ethanethiol; n-butyllithium / N,N,N,N,N,N-hexamethylphosphoric triamide / 2 h / 0 - 70 °C / Inert atmosphere

2.1: sodium hydride / N,N-dimethyl-formamide / 0.17 h / 0 °C

2.2: 2 h / 0 - 20 °C

3.1: ethanethiol; n-butyllithium / N,N,N,N,N,N-hexamethylphosphoric triamide / 2 h / 0 - 70 °C / Inert atmosphere

With n-butyllithium; sodium hydride; ethanethiol; In N,N,N,N,N,N-hexamethylphosphoric triamide; N,N-dimethyl-formamide;
DOI:10.1016/j.tet.2013.05.024