507-79-9

Basic information

• Product Name: tazettine
• Synonyms: (+)-Tazettine; 507-79-9; Sekisanine; Tazettin
• CAS NO: 507-79-9
• Molecular Formula: C₁₈H₂₁NO₅
• Molecular Weight: 331.363
• Mol File: 507-79-9.mol
• Article Data: 5

Chemical Properties

• Melting Point: 210-211° (evac tube); mp 237-238° (Tsuda) and mp 175-176° (Danishefsky)
• Boiling Point: 494.2°C at 760 mmHg
• Flash Point: 252.7°C
• Density: 1.41g/cm³
• Vapor Pressure: 1.39E-10mmHg at 25°C
• Refractive Index: 1.66
• PKA: 11.89±0.40(Predicted)
• CAS DataBase Reference: tazettine(CAS DataBase Reference)
• NIST Chemistry Reference: tazettine(507-79-9)
• EPA Substance Registry System: tazettine(507-79-9)

Safety Data

• Hazardous Substances Data: 507-79-9(Hazardous Substances Data)

Usage

Description

Tazettine is an alkaloid found in the Amaryllidaceae family, particularly in Narcissus species. It is known to be an extraction artifact of pretazettine and is characterized by the presence of a typical methylenedioxy group between the C-8 and C-9 positions. Tazettine-type alkaloids, including obesine, are of interest due to their unique chemical structures and potential applications.

Uses

Used in Pharmaceutical Industry:
Tazettine is used as a pharmaceutical compound for its potential therapeutic properties. The expression is: tazettine is used as a pharmaceutical compound for its potential therapeutic properties.
Used in Research and Development:
Tazettine is used as a research compound for studying its chemical properties and exploring its potential applications in various fields. The expression is: tazettine is used as a research compound for studying its chemical properties and exploring its potential applications.
Used in Natural Product Extraction:
Tazettine is used as a natural product extracted from the Amaryllidaceae family, particularly Narcissus species, for further analysis and potential utilization in various industries. The expression is: tazettine is used as a natural product extracted from the Amaryllidaceae family for further analysis and potential utilization.

Upstream product

• 50-00-0 formaldehyd 
• 64-18-6 formic acid 
• 466-73-9 6-epihaemanthidine 
• 67-56-1 methanol 
• 74-88-4 methyl iodide 
• 17245-16-8 pretazettine 
• 21850-90-8 pretazettine 
• 466-73-9 (+)-haemanthidine 
• 17322-84-8 pretazettine 
• 73060-68-1 3α-hydroxy-3aβ-(2-hydroxymethyl-4,5-methylenedioxyphenyl)-6β-methoxy-N-methyl-2,3,6,7-tetrahydro-7aH-indole 
• 7732-18-5 water 
• 23315-34-6 ent-(11Ξ)-6β,11-dihydroxy-3β-methoxy-5-methyl-crin-1-enium; iodide 
• 1472-71-5 (4aS)-3t-methoxy-(4ar,13btC¹)-4,4a,5,6-tetrahydro-3H,8H-[1,3]dioxolo[4',5':6,7]isochromeno[3,4-c]indol-6at-ol 
• 466-73-9 ent-(11S)-3β-methoxy-crin-1-ene-6β,11-diol 

Downstream Products

• 65367-81-9 N-Methyl-8,9-methylenedioxy-phenantridinium chloride 
• 86046-50-6 4,5-methylenedioxy-4'-hydroxy-2-aldehyde[1,1'-biphenyl] 
• 124339-69-1 (4aS)-6a-hydroxy-3t-methoxy-5,5-dimethyl-(4ar,6at,13btC¹)-3,4,4a,5,6,6a-hexahydro-8H-[1,3]dioxolo[4',5':6,7]isochromeno[3,4-c]indolium; picrate 
• 466-66-0 tazettadiol 
• 73060-68-1 3α-hydroxy-3aβ-(2-hydroxymethyl-4,5-methylenedioxyphenyl)-6β-methoxy-N-methyl-2,3,6,7-tetrahydro-7aH-indole 
• 4371-22-6 (6-phenyl-benzo[1,3]dioxol-5-yl)-methanol 
• 144-62-7 oxalic acid 
• 4371-22-6 6-phenylpiperonylalcohol 
• 40141-98-8 N-methylcrinasiadine 

Relevant articles and documents

Total syntheses of (-)-haemanthidine, (+)-pretazettine, and (+)-tazettine

(matrix presented) Haemanthidine Pretazettine Tazettine The total syntheses of the amaryllidaceae alkaloids haemanthidine, pretazettine, and tazettine as optically pure enantiomers are reported. Using D-mannose as the starting material, the critical relat

ALKALOIDS FROM NARCISSUS CONFUSUS

Key Word Index - Narcissus confusus; Amaryllidaceae; haemanthamine; galanthamine; N-formylgalanthamine; pretazettine; two-dimensional NMR spectra.We report the isolation of haemanthamine, galanthamine, pretazettine and the new alkaloid N-formylgalanthamine from Narcissus confusus plants.Structural determination was carried out by spectroscopic analyses and application of two-dimensional NMR spectroscopy.

Transformation of tazettine to pretazettine

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