Proanthocyanidin A5'

Base Information

Chemical Name:Proanthocyanidin A5'
CAS No.:111466-30-9
Molecular Formula:C30H24 O12
Molecular Weight:576.513
Hs Code.:
Nikkaji Number:J413.401J
Wikidata:Q105184981
Metabolomics Workbench ID:47866
Mol file:111466-30-9.mol

Synonyms:Proanthocyanidin A5';(1S,5R,6R,13R,21S)-5,13-bis(3,4-dihydroxyphenyl)-4,12,14-trioxapentacyclo[11.7.1.02,11.03,8.015,20]henicosa-2(11),3(8),9,15,17,19-hexaene-6,9,17,19,21-pentol;111466-30-9;SCHEMBL15399757;CHEBI:191732;(+)-Epicatechin-(2a-7)(4a-8)-epicatechin;Ent-Epicatechin-(2a->7,4a->8)-epicatechin;(1S,5R,6R,13R,21S)-5,13-bis(3,4-dihydroxyphenyl)-4,12,14-trioxapentacyclo[11.7.1.0^{2,11}.0^{3,8}.0^{15,20}]henicosa-2,8,10,15,17,19-hexaene-6,9,17,19,21-pentol;(2R,15S)-3,4-Dihydro-2alpha,8-bis(3,4-dihydroxyphenyl)-8alpha,14alpha-methano-2H,14H-1-benzopyrano[7,8-d][1,3]benzodioxocin-3alpha,5,11,13,15-pentol

Suppliers and Price of Proanthocyanidin A5'

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 1 raw suppliers

Chemical Property of Proanthocyanidin A5'

Chemical Property:

PSA：209.76000
LogP:2.79350
XLogP3:2.4
Hydrogen Bond Donor Count:9
Hydrogen Bond Acceptor Count:12
Rotatable Bond Count:2
Exact Mass:576.12677620
Heavy Atom Count:42
Complexity:986

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1C(C(OC2=C1C(=CC3=C2C4C(C(O3)(OC5=CC(=CC(=C45)O)O)C6=CC(=C(C=C6)O)O)O)O)C7=CC(=C(C=C7)O)O)O
Isomeric SMILES:C1[C@H]([C@H](OC2=C1C(=CC3=C2[C@H]4[C@@H]([C@@](O3)(OC5=CC(=CC(=C45)O)O)C6=CC(=C(C=C6)O)O)O)O)C7=CC(=C(C=C7)O)O)O

Technology Process of Proanthocyanidin A5'

There total 1 articles about Proanthocyanidin A5' 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: 92.0%