Artemin

Base Information

Chemical Name:Artemin
CAS No.:22149-38-8
Molecular Formula:C₁₅H₂₂O₄
Molecular Weight:266.337
Hs Code.:
Wikidata:Q104252396
Metabolomics Workbench ID:46645
ChEMBL ID:CHEMBL1595875
Mol file:22149-38-8.mol

Synonyms:artemin;6,9a-dihydroxy-3,5a-dimethyl-9-methylidene-3,3a,4,5,6,7,8,9b-octahydrobenzo[g][1]benzofuran-2-one;Isogallicadiol;22149-38-8;6,9a-dihydroxy-3,5a-dimethyl-9-methylenedecahydronaphtho[1,2-b]furan-2(3H)-one;Artemine;11S-Artemin;Artemin (sesquiterpene);Oprea1_752585;MLS001195108;CHEMBL1595875;CHEBI:168328;HMS1607C03;HMS2864H06;NCGC00245791-01;SMR000554415;(11a)-1b,5a-Dihydroxy-4(15)-eudesmen-12,6a-olide;6,9a-dihydroxy-3,5a-dimethyl-9-methylidene-dodecahydronaphtho[1,2-b]furan-2-one;[3S-(3alpha,3aalpha,5abeta,6beta,9aalpha,9bbeta)]-Decahydro-6,9a-dihydroxy-3,5a-dimethyl-9-methylenenaphtho[1,2-b]furan-2(3H)-one;6,9a-dihydroxy-3,5a-dimethyl-9-methylidene-3,3a,4,5,6,7,8,9b-octahydrobenzo[g][1]benzouran-2-one

Suppliers and Price of Artemin

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

Usbiological
Artemin
96Tests
$ 864.00

Usbiological
Artemin
10ug
$ 333.00

Usbiological
Artemin
10ug
$ 327.00

Total 0 raw suppliers

Chemical Property of Artemin

Chemical Property:

PSA：66.76000
LogP:1.40620
Storage Temp.:-20°C
XLogP3:1.1
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:0
Exact Mass:266.15180918
Heavy Atom Count:19
Complexity:445

Purity/Quality:: Artemin ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:Xn
Statements: 22

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1C2CCC3(C(CCC(=C)C3(C2OC1=O)O)O)C

Technology Process of Artemin

There total 4 articles about Artemin 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:

: 553-21-9
costunolide

: 22149-38-8
artemin

Guidance literature:: Multi-step reaction with 4 steps

1: 1.) m-ClC₆H₄O₃H, 2.) SOCl₂

2: 106 mg / oxygen, methylene blue / ethanol / 7 h / Irradiation

3: 40 mg / triphenylphosphine / acetone / 0.5 h

4: sodium borohydride

With sodium tetrahydroborate; thionyl chloride; oxygen; methylene blue; 3-chloro-benzenecarboperoxoic acid; triphenylphosphine; In ethanol; acetone;

Reference yield:

: 85847-67-2
1β-hydroxy-5α-hydroperoxy-6β,7αH-eudesma-4(15),11(13)dien-12,6-olide

: 22149-38-8
artemin

Guidance literature:: Multi-step reaction with 2 steps

1: 40 mg / triphenylphosphine / acetone / 0.5 h

2: sodium borohydride

With sodium tetrahydroborate; triphenylphosphine; In acetone;

Reference yield:

: 95782-68-6,125356-46-9,72145-13-2
1β-hydroxy-5α,6β,7αH-eudesma-4(5),11(13)-dien-12,6-olide

: 22149-38-8
artemin

Guidance literature:: Multi-step reaction with 3 steps

1: 106 mg / oxygen, methylene blue / ethanol / 7 h / Irradiation

2: 40 mg / triphenylphosphine / acetone / 0.5 h

3: sodium borohydride

With sodium tetrahydroborate; oxygen; methylene blue; triphenylphosphine; In ethanol; acetone;