oxyacanthine

Product Name
oxyacanthine
CAS No.
548-40-3
Chemical Name
oxyacanthine
Synonyms
vinetine;Oxycanthine;oxyacanthine;6,6',7-Trimethoxy-2,2'-dimethyloxyacanthan-12'-ol;2H-1,24:12,15-Dietheno-6,10-metheno-16H-pyrido[2',3':17,18][1,10]dioxacycloeicosino[2,3,4-ij]isoquinolin-9-ol, 3,4,4a,5,16a,17,18,19-octahydro-21,22,26-trimethoxy-4,17-dimethyl-, (4aR,16aS)-
CBNumber
CB0902883
Molecular Formula
C37H40N2O6
Formula Weight
608.72
MOL File
548-40-3.mol
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oxyacanthine Property

Melting point:
216-217°
alpha 
D20 +131.5° (chloroform)
Boiling point:
655.15°C (rough estimate)
Density 
1.1648 (rough estimate)
refractive index 
1.5300 (estimate)
pka
9.42±0.20(Predicted)
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

American Custom Chemicals Corporation
Product number
PXT0002048
Product name
OXYACANTHINE
Purity
95.00%
Packaging
5MG
Price
$503.9
Updated
2021/12/16
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oxyacanthine Chemical Properties,Usage,Production

Description

This alkaloid was first obtained by Hesse from Berberis vulgaris and is also a minor constituent of other Berberis and Mahonia species. When recrystallized from EtOH it forms clusters of colourless needles, m.p. 208-214°C, the higher melting point given above being obtained in vacuo. It has [α]D + 131.6° (CHC13), a much higher value of + 279° (CHCI3) being given by Gericke and Bruchhausen. The dihydrochloride forms needles, m.p. 270-1°C (vac.); [α] +29 D+ 188.5° (H20) and is only sparingly soluble in dilute HC1; the hydrobromide has m.p. 273-5°C (dec., vac.) and the nitrate forms colourless needles, m.p. 195- 200°C (dec.). The presence of the phenolic hydroxyl group is indicated by the formation of an O-benzoy1 derivative, a potassium salt and the O-methyl ether, giving a hydrochloride, m.p. 261°C. The structure has been deduced from chem_x0002_ical and spectroscopic data. Various colour reactions have been described, e.g. the alkaloid is not coloured by H2S04, gives a yellow colour with HN03 and with molybdic acid in H2S04 produces a violet colour, slowly changing to yellow-green.

Definition

ChEBI: A macrocycle that is oxyacanthan that is substituted by methoxy groups at positions 6, 6', and 7, methyl groups at positions 2 and 2', and a hydroxy group at the 12' position.

oxyacanthine Preparation Products And Raw materials

Raw materials

Preparation Products

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oxyacanthine Suppliers

Interbioscreen Ltd.
Tel
--
Fax
--
Email
screen@ibscreen.chg.ru
Country
Finland
ProdList
6176
Advantage
60

548-40-3, oxyacanthineRelated Search:


  • 6,6',7-Trimethoxy-2,2'-dimethyloxyacanthan-12'-ol
  • Oxycanthine
  • oxyacanthine
  • vinetine
  • 2H-1,24:12,15-Dietheno-6,10-metheno-16H-pyrido[2',3':17,18][1,10]dioxacycloeicosino[2,3,4-ij]isoquinolin-9-ol, 3,4,4a,5,16a,17,18,19-octahydro-21,22,26-trimethoxy-4,17-dimethyl-, (4aR,16aS)-
  • 548-40-3