(2R)-Taxiphyllin

Base Information

Chemical Name:(2R)-Taxiphyllin
CAS No.:21401-21-8
Molecular Formula:C₁₄H₁₇NO₇
Molecular Weight:311.291
Hs Code.:
Wikidata:Q105186300
Mol file:21401-21-8.mol

Synonyms:(2R)-Taxiphyllin;Phyllanthoside?;Phyllanthin?;SCHEMBL12727838;ZINC00895585;FT-0770936;FT-0774926;B0005-189732

Suppliers and Price of (2R)-Taxiphyllin

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

Arctom
Taxiphyllin
5mg
$ 463.00

Total 20 raw suppliers

Chemical Property of (2R)-Taxiphyllin

Chemical Property:

Vapor Pressure:1.32E-14mmHg at 25°C
Melting Point:137 - 140 °C (methanol)
Boiling Point:586.7°Cat760mmHg
Flash Point:308.6°C
PSA：143.40000
Density:1.56g/cm³
LogP:-1.22662
XLogP3:-0.9
Hydrogen Bond Donor Count:5
Hydrogen Bond Acceptor Count:8
Rotatable Bond Count:4
Exact Mass:311.10050188
Heavy Atom Count:22
Complexity:403

Purity/Quality:

98%min ^*data from raw suppliers

Taxiphyllin ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC(=CC=C1C(C#N)OC2C(C(C(C(O2)CO)O)O)O)O

Technology Process of (2R)-Taxiphyllin

There total 5 articles about (2R)-Taxiphyllin 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:

: 67-56-1
methanol

: taxiphyllin 6'-O-gallate

: 99-24-1
methyl galloate

: 499-20-7,13115-69-0,21401-21-8
(2R)-2-(β-D-glucopyranosyloxy)-4-hydroxyphenylacetonitrile

Guidance literature:: With sodium methylate; at 20 ℃; for 4h;
DOI:10.1248/cpb.c14-00352

Reference yield:

: 29883-15-6,672-72-0
amygdalin

: 499-20-7,13115-69-0,21401-21-8
(2R)-2-(β-D-glucopyranosyloxy)-4-hydroxyphenylacetonitrile

Guidance literature:: With extracellular enzymes from Aspergillus niger; at 37 ℃; for 4h;
DOI:10.1016/j.procbio.2011.10.030

Reference yield:

: 878-00-2
4-formylphenyl acetate

: 499-20-7,13115-69-0,21401-21-8
(2R)-2-(β-D-glucopyranosyloxy)-4-hydroxyphenylacetonitrile

Guidance literature:: Multi-step reaction with 3 steps

1: lithium perchlorate / neat (no solvent) / 0.5 h / 20 °C / Inert atmosphere

2: boron trifluoride diethyl etherate / dichloromethane / 2 h / 20 °C / Inert atmosphere

3: trifluorormethanesulfonic acid; methanol / 3 h / 20 °C / Inert atmosphere

With methanol; trifluorormethanesulfonic acid; boron trifluoride diethyl etherate; lithium perchlorate; In dichloromethane;
DOI:10.1021/acs.jnatprod.5b01121