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2,4-Methano-4H-furo(3,2-b)pyrrole, hexahydro-3-(methylamino)-

Base Information Edit
  • Chemical Name:2,4-Methano-4H-furo(3,2-b)pyrrole, hexahydro-3-(methylamino)-
  • CAS No.:25161-91-5
  • Molecular Formula:C8H14N2O
  • Molecular Weight:154.212
  • Hs Code.:
  • DSSTox Substance ID:DTXSID30948022
  • Mol file:25161-91-5.mol
2,4-Methano-4H-furo(3,2-b)pyrrole, hexahydro-3-(methylamino)-

Synonyms:DTXSID30948022;N-methylhexahydro-1H-1,6-epoxypyrrolizin-7-amine

Suppliers and Price of 2,4-Methano-4H-furo(3,2-b)pyrrole, hexahydro-3-(methylamino)-
Supply Marketing:Edit
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
  • Loline
  • 5mg
  • $ 418.00
  • American Custom Chemicals Corporation
  • LOLINE 95.00%
  • 5MG
  • $ 499.38
Total 5 raw suppliers
Chemical Property of 2,4-Methano-4H-furo(3,2-b)pyrrole, hexahydro-3-(methylamino)- Edit
Chemical Property:
  • Boiling Point:232.6°Cat760mmHg 
  • PKA:9.36±0.20(Predicted) 
  • Flash Point:94.5°C 
  • PSA:24.50000 
  • Density:1.2g/cm3 
  • LogP:-0.24150 
  • XLogP3:-0.4
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:1
  • Exact Mass:154.110613074
  • Heavy Atom Count:11
  • Complexity:185
Purity/Quality:

99% *data from raw suppliers

Loline *data from reagent suppliers

Safty Information:
  • Pictogram(s): A poison. 
  • Hazard Codes:A poison. 
MSDS Files:
Useful:
  • Canonical SMILES:CNC1C2CN3C1C(O2)CC3
  • Isomeric SMILES:CN[C@H]1[C@H]2CN3[C@@H]1C(O2)CC3
  • Description This oily alkaloid has been obtained from a species of grass, Lotium cuneatum Nevski. It has a density of D 20 1.1343 and a refractive index of n20D 1.5505. It behaves as a diacidic base yielding a series of well crystalline salts and derivatives, e.g. the dihydrochloride, m.p. 256-7°C; [α]15D + 6.2° (H20); dihydrobromide, m.p. 254-5°C (dec.); [α]20D + 3.5° (c 4.29, H20); dihydriodide, m.p. 233-5°C (dec.); [α]34D + 5.0° (c 13.2 H20); perchlorate, m.p. 282°C with almost explosive decomposition; sulphate, yellow needles, m.p. 250-2°C (dec.); mononitrate,m.p. 208-2l0°C; dinitrate, m.p. l48-9°C; [α]38D + 6.18° (c 6.94, H20); dipicrate, m.p. 258-260°C (dec.); methiodide, m.p. 2l0-loC and the N-nitroso derivative, m.p. 64°C. The N-acetyl derivative yields a crystalline hydrochloride, m.p. 197-8°C; [α]20D + 36.9° (H20) and the N-methyl compound is obtained as a colourless oil, b.p. 90-l oC/2 mm; [α]31D+ 9.31° (c 9.5, MeOH). The alkaloid possesses an ether oxygen bridging the pyrrolizidine moiety.
Technology Process of 2,4-Methano-4H-furo(3,2-b)pyrrole, hexahydro-3-(methylamino)-

There total 15 articles about 2,4-Methano-4H-furo(3,2-b)pyrrole, hexahydro-3-(methylamino)- 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:
Guidance literature:
With sodium naphthalenide; In 1,2-dimethoxyethane; at -60 ℃; for 0.333333h;
Guidance literature:
Multi-step reaction with 2 steps
1: 74 percent / 1,2-dichloro-benzene / 22 h / 180 °C
2: sodium naphthalenide / 1,2-dimethoxy-ethane / 0.33 h / -60 °C
With sodium naphthalenide; In 1,2-dimethoxyethane; 1,2-dichloro-benzene;
Guidance literature:
Multi-step reaction with 6 steps
1: 99 percent / Et3N / CH2Cl2 / 0.25 h / 0 °C
2: BH3*SMe2 / tetrahydrofuran / 5 h / 20 °C
3: 15.0 mg / Pd(OH)2/C / methanol / 14 h / 20 °C
4: 70 percent / DDQ; H2O / CH2Cl2 / 64 h / 20 °C
5: 74 percent / 1,2-dichloro-benzene / 22 h / 180 °C
6: sodium naphthalenide / 1,2-dimethoxy-ethane / 0.33 h / -60 °C
With dimethylsulfide borane complex; water; sodium naphthalenide; triethylamine; 2,3-dicyano-5,6-dichloro-p-benzoquinone; palladium dihydroxide; In tetrahydrofuran; methanol; 1,2-dimethoxyethane; dichloromethane; 1,2-dichloro-benzene;
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