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(1.1.1)Propellane

Base Information Edit
  • Chemical Name:(1.1.1)Propellane
  • CAS No.:35634-10-7
  • Molecular Formula:C5H6
  • Molecular Weight:66.1026
  • Hs Code.:
  • UNII:B99AQN9D35
  • DSSTox Substance ID:DTXSID20189149
  • Nikkaji Number:J264.146A
  • Wikipedia:1.1.1-Propellane
  • Wikidata:Q4545828
  • Mol file:35634-10-7.mol
(1.1.1)Propellane

Synonyms:(1.1.1)Propellane;Tricyclo[1.1.1.01,3]pentane;35634-10-7;[1.1.1]Propellane;1.1.1-propellane;B99AQN9D35;tricyclo[1.1.1.0(1,3)]pentane;[1.1.1] propellane;UNII-B99AQN9D35;DTXSID20189149;F71090;Q4545828

Suppliers and Price of (1.1.1)Propellane
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
Total 7 raw suppliers
Chemical Property of (1.1.1)Propellane Edit
Chemical Property:
  • Vapor Pressure:143mmHg at 25°C 
  • Boiling Point:69.9°Cat760mmHg 
  • Flash Point:°C 
  • PSA:0.00000 
  • Density:1.2g/cm3 
  • LogP:1.17030 
  • XLogP3:1.4
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:0
  • Rotatable Bond Count:0
  • Exact Mass:66.0469501914
  • Heavy Atom Count:5
  • Complexity:73.2
Purity/Quality:

99%, *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:C1C23C1(C2)C3
  • Uses Tricyclo[1.1.1.01,?3]?pentane can be used to produce thermoplastic compounds containing ethylene response inhibitor releasing material.
Technology Process of (1.1.1)Propellane

There total 2 articles about (1.1.1)Propellane 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; lithium; In decane; at 73 ℃; for 1.5h; under 14 Torr; Yield given. Further byproducts given;
Guidance literature:
In diethyl ether; at 20 ℃; for 0.25h;
DOI:10.3762/bjoc.15.114
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