Sarranicine

Base Information

• Chemical Name: Sarranicine
• CAS No.: 2492-09-3
• Molecular Formula: C₁₈H₂₇NO₅
• Molecular Weight: 337.416
• DSSTox Substance ID: DTXSID201019749
• Nikkaji Number: J846.807I
• Wikidata: Q76386784
• Mol file: 2492-09-3.mol

Synonyms:2-(hydroxymethyl)-hexahydro-7-((2-methyl-1-oxo-2-butenyl)oxy)-1H-pyrrolizin-1-yl-2-butenoic acid;sarracine;sarracine monotartrate;sarracine tartrate (2:1)

Chemical Property of Sarranicine

Chemical Property:

• Vapor Pressure: 2.64E-10mmHg at 25°C
• Boiling Point: 457.8°Cat760mmHg
• Flash Point: 230.7°C
• PSA: 76.07000
• Density: 1.18g/cm³
• LogP: 1.37830
• XLogP3: 1.8
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 8
• Exact Mass: 337.18892296
• Heavy Atom Count: 24
• Complexity: 540

Purity/Quality:

99%, ^*data from raw suppliers

SARRACINE 95.00% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC=C(C)C(=O)OC1CCN2C1C(CC2)COC(=O)C(=CC)CO
• Isomeric SMILES: C/C=C(\C)/C(=O)O[C@@H]1CCN2[C@@H]1[C@H](CC2)COC(=O)/C(=C\C)/CO
• Description: The structure of this pyrrolizidine alkaloid has been determined as that illustrated above which is based upon chemical analysis and spectroscopic investigations.

Technology Process of Sarranicine

There total 2 articles about Sarranicine 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:

→ Sarracin (2492-09-3,136173-25-6,136173-26-7,136173-27-8)

Guidance literature:

Sarracin-N-oxid, Zn/H⁺;

Reference yield:

→ sarracine (2492-09-3)

Guidance literature:

DOI:10.1021/jo01067a001