Welcome to LookChem.com Sign In|Join Free
  • or

Encyclopedia

Azacyclododecan-2-one

Base Information
  • Chemical Name:Azacyclododecan-2-one
  • CAS No.:1202-71-7
  • Molecular Formula:C11H21NO
  • Molecular Weight:183.294
  • Hs Code.:2933790090
  • DSSTox Substance ID:DTXSID70501418
  • Nikkaji Number:J13.165B
  • Mol file:1202-71-7.mol
Azacyclododecan-2-one

Synonyms:Azacyclododecan-2-one;1202-71-7;1-AZACYCLODODECAN-2-ONE;undecalactam;Undecyclolactam;SCHEMBL249693;SCHEMBL16417238;DTXSID70501418;BAA20271;AKOS016344579;6-Isopropyl-5-methylthiomorpholin-3-one;AS-57444;BB 0262704;CS-0196563

Suppliers and Price of Azacyclododecan-2-one
Supply Marketing:
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 11 raw suppliers
Chemical Property of Azacyclododecan-2-one
Chemical Property:
  • Boiling Point:302.517 °C at 760 mmHg 
  • Flash Point:178.798 °C 
  • PSA:32.59000 
  • Density:0.892 g/cm3 
  • LogP:2.90300 
  • Storage Temp.:Sealed in dry,Room Temperature 
  • XLogP3:2.3
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:1
  • Rotatable Bond Count:0
  • Exact Mass:183.162314293
  • Heavy Atom Count:13
  • Complexity:145
Purity/Quality:

98%,99%, *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:C1CCCCCNC(=O)CCCC1
  • General Description 1-Azacyclododecan-2-one, also known as undecylolactam or undecanolactam, is a 12-membered lactam that can be synthesized more efficiently in aqueous solutions using cavitand templates, which enhance cyclization by promoting folded conformations of ω-amino acids. This approach improves yields significantly compared to traditional methods, demonstrating the potential for facilitating medium-sized lactam formation in water despite the inherent challenges of ring strain and competing intermolecular reactions. The use of cavitands represents a promising strategy for conducting dehydration-involved organic reactions in aqueous environments.
Technology Process of Azacyclododecan-2-one

There total 21 articles about Azacyclododecan-2-one 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:
per-rhenic acid; 3,5-bis-trifluromethylphenylboronic acid; In acetonitrile; at 120 ℃; for 4h; Product distribution / selectivity; Heating / reflux;
Guidance literature:
With hydrogenchloride; sodium azide; In 1,2-dimethoxyethane;
DOI:10.1021/jo00158a022
Guidance literature:
With 1,3,5-trichloro-2,4,6-triazine; zinc(II) chloride; In acetonitrile; for 1h; Heating;
DOI:10.1021/ja053441x
Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 1202-71-7