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Encyclopedia

Cyclorphan

Base Information Edit
  • Chemical Name:Cyclorphan
  • CAS No.:4163-15-9
  • Molecular Formula:C20H27NO
  • Molecular Weight:297.44
  • Hs Code.:
  • European Community (EC) Number:224-007-5
  • UNII:U6Z73N36V0
  • DSSTox Substance ID:DTXSID50878519
  • Wikipedia:Cyclorphan
  • Wikidata:Q5199001
  • Pharos Ligand ID:2VSAJRHK6SR7
  • ChEMBL ID:CHEMBL49269
  • Mol file:4163-15-9.mol
Cyclorphan

Synonyms:cyclorphan

Suppliers and Price of Cyclorphan
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
  • American Custom Chemicals Corporation
  • CYCLORPHAN 95.00%
  • 5MG
  • $ 505.59
Total 8 raw suppliers
Chemical Property of Cyclorphan Edit
Chemical Property:
  • Melting Point:187.5-189° 
  • Refractive Index:1.5614 (estimate) 
  • Boiling Point:438.94°C (rough estimate) 
  • PSA:23.47000 
  • Density:1.0234 (rough estimate) 
  • LogP:3.79850 
  • XLogP3:3.9
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:2
  • Exact Mass:297.209264485
  • Heavy Atom Count:22
  • Complexity:433
Purity/Quality:

98%Min *data from raw suppliers

CYCLORPHAN 95.00% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:C1CCC23CCN(C(C2C1)CC4=C3C=C(C=C4)O)CC5CC5
  • Isomeric SMILES:C1CC[C@@]23CCN([C@@H]([C@@H]2C1)CC4=C3C=C(C=C4)O)CC5CC5
Technology Process of Cyclorphan

There total 10 articles about Cyclorphan 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 lithium aluminium tetrahydride;
DOI:10.1016/S0031-6865(99)00044-8
Guidance literature:
Multi-step reaction with 2 steps
1: Et3N / CH2Cl2 / 14 h / Heating
2: LiAlH4 / tetrahydrofuran / 20 °C
With lithium aluminium tetrahydride; triethylamine; In tetrahydrofuran; dichloromethane;
DOI:10.1021/jm9903343
Guidance literature:
Multi-step reaction with 5 steps
1.1: 99 percent / diethyl ether; methanol / 20 °C
2.1: NaHCO3; 1-chloroethyl chloroformate / 1,2-dichloro-ethane / 48 h / Heating
2.2: 90 percent / MeOH / 3 h / Heating
3.1: HBr; AcOH
4.1: Et3N / CH2Cl2 / 14 h / Heating
5.1: LiAlH4 / tetrahydrofuran / 20 °C
With lithium aluminium tetrahydride; carbonochloridic acid 1-chloro-ethyl ester; hydrogen bromide; sodium hydrogencarbonate; acetic acid; triethylamine; In tetrahydrofuran; methanol; diethyl ether; dichloromethane; 1,2-dichloro-ethane;
DOI:10.1021/jm9903343
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