Batatasin I

Base Information

Chemical Name:Batatasin I
CAS No.:51415-00-0
Molecular Formula:C17H16O4
Molecular Weight:284.31
Hs Code.:2909499000
UNII:26K4DP7BUA
DSSTox Substance ID:DTXSID00199403
Nikkaji Number:J11.651C
Wikidata:Q27105919
Metabolomics Workbench ID:48332
Mol file:51415-00-0.mol

Synonyms:6-hydroxy-2,4,7-trimethoxyphenanthrene;batatasin I

Suppliers and Price of Batatasin I

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 21 raw suppliers

Chemical Property of Batatasin I

Chemical Property:

Vapor Pressure:2.27E-10mmHg at 25°C
Refractive Index:1.656
Boiling Point:493.7 °C at 760 mmHg
PKA:9.33±0.30(Predicted)
Flash Point:252.4 °C
PSA：47.92000
Density:1.246 g/cm³
LogP:3.72440
XLogP3:4
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:3
Exact Mass:284.10485899
Heavy Atom Count:21
Complexity:348

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:COC1=CC(=C2C(=C1)C=CC3=CC(=C(C=C32)O)OC)OC
Uses Batatasin I is a naturally occurring phenanthrene derivative that is isolated from tuberous roots of Dioscorea batatas. It suppresses eicosanoids generation and degranulation in bone marrow derived-mast cells and has potential antimicrobial activity.

Technology Process of Batatasin I

There total 3 articles about Batatasin 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:

: 4-benzyloxy-3,3',5-trimethoxystibene

: 51415-00-0
batatasin I

Guidance literature:: 4-benzyloxy-3,3',5-trimethoxystibene; With iodine; In cyclohexane; for 8h; UV-irradiation;

With palladium on activated charcoal; hydrogen; In methanol; at 20 ℃; for 12h;
DOI:10.1039/c5ra15328j