1,4-Diazabicyclo[3.2.2]nonan-3-one

Base Information

• Chemical Name: 1,4-Diazabicyclo[3.2.2]nonan-3-one
• CAS No.: 53619-11-7
• Molecular Formula: C7H12N2O
• Molecular Weight: 140.185
• Hs Code.: 2933990090
• DSSTox Substance ID: DTXSID30402876
• Nikkaji Number: J2.283.635H
• Wikidata: Q72463195
• Mol file: 53619-11-7.mol

Synonyms:1,4-diazabicyclo[3.2.2]nonan-3-one;53619-11-7;3-Oxo-1,4-diazabicyclo[3.2.2]nonane;MFCD01815127;SCHEMBL231694;DTXSID30402876;STL353503;AKOS000425355;1,4-Diazabicyclo[3.2.2]nonane-3-one;SY129252;AM20100321;CS-0116768;FT-0730702;EN300-160362;A829690

Chemical Property of 1,4-Diazabicyclo[3.2.2]nonan-3-one

Chemical Property:

• Vapor Pressure: 0.000362mmHg at 25°C
• Boiling Point: 318.4oC at 760 mmHg
• Flash Point: 146.4°C
• PSA: 32.34000
• Density: 1.17g/cm³
• LogP: -0.15270
• XLogP3: -0.1
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 0
• Exact Mass: 140.094963011
• Heavy Atom Count: 10
• Complexity: 150

Purity/Quality:

98%Min ^*data from raw suppliers

1,4-Diazabicyclo[3.2.2]nonan-3-one ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1CN2CCC1NC(=O)C2

Technology Process of 1,4-Diazabicyclo[3.2.2]nonan-3-one

There total 1 articles about 1,4-Diazabicyclo[3.2.2]nonan-3-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:

Reference yield: 24.0%

1-azabicyclo<2.2.2>octan-3-one oxime (78961-49-6) → piperidin-1-yl-acetonitrile (3010-03-5) + 1,4-diaza-bicyclo[3.2.2]nonan-3-one (53619-11-7)

Guidance literature:

With sulfuric acid; at 180 ℃; for 0.25h; microwave irradiation;

DOI:10.1080/00397910500377255

Reference yield: 98.0%

1,4-diaza-bicyclo[3.2.2]nonan-3-one (53619-11-7) → 1,4-diazabicyclo[3.2.2]nonane (283-38-5)

Guidance literature:

With lithium aluminium tetrahydride; In tetrahydrofuran; for 2h; Heating;

DOI:10.1080/00397910500377255

Reference yield: 20.0%

3,6-dibromopyridazine (17973-86-3) + 1,4-diaza-bicyclo[3.2.2]nonan-3-one (53619-11-7) → 4-(6-bromo-pyridazin-3-yl)-1, 4-diazabicyclo [3.2. 2] nonane (695184-05-5)

Guidance literature:

With sodium hydroxide; In water; at 100 ℃; for 0.5h;

upstream raw materials:

1-azabicyclo<2.2.2>octan-3-one oxime

Downstream raw materials:

1,4-diazabicyclo[3.2.2]nonane

4-(6-bromo-pyridazin-3-yl)-1, 4-diazabicyclo [3.2. 2] nonane

(4-([1,1'-biphenyl]-4-yl)piperazin-1-yl)(1,4-diazabicyclo[3.2.2]nonan-4-yl)methanone

N-(2-(3-(prop-1-en-2-yl)phenyl)propan-2-yl)-1,4-diazabicyclo[3.2.2]nonane-4-carboxamide