(1S,2S,5R,6R)-3-AZATRICYCLO[4.2.1.0(2,5)]NON-7-EN-4-ONE

Base Information

Chemical Name:(1S,2S,5R,6R)-3-AZATRICYCLO[4.2.1.0(2,5)]NON-7-EN-4-ONE
CAS No.:924272-78-6
Molecular Formula:C₈H₉NO
Molecular Weight:135.166
Hs Code.:
Mol file:924272-78-6.mol

Synonyms:(1S,2S,5R,6R)-3-AZATRICYCLO[4.2.1.0(2,5)]NON-7-EN-4-ONE

Suppliers and Price of (1S,2S,5R,6R)-3-AZATRICYCLO[4.2.1.0(2,5)]NON-7-EN-4-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

TRC
(1S,2S,5R,6R)-3-Azatricyclo[4.2.1.02,5]non-7-en-4-one
1mg
$ 95.00

American Custom Chemicals Corporation
(1S,2S,5R,6R)-3-AZATRICYCLO[4.2.1.0(2,5)]NON-7-EN-4-ONE 95.00%
5MG
$ 496.50

Total 0 raw suppliers

Chemical Property of (1S,2S,5R,6R)-3-AZATRICYCLO[4.2.1.0(2,5)]NON-7-EN-4-ONE

Chemical Property:

Melting Point:90-93 °C
Boiling Point:332.2±42.0 °C (760 mmHg)
PSA：29.10000
Density:1.256±0.06 g/cm3 (20 °C, 760 mmHg)
LogP:0.63570

Purity/Quality:: (1S,2S,5R,6R)-3-Azatricyclo[4.2.1.02,5]non-7-en-4-one ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Uses (1S,2S,5R,6R)-3-Azatricyclo[4.2.1.02,5]non-7-en-4-one is a carbocyclic β-lactam. It is used in the asymmetric synthesis of enantiopure carbocyclic β-amino acids via Candida antarctica lipase catalyzed solvent-free vapor-assisted enantioselective hydrolytic ring opening of carbocyclic β-lactams. (1S,2S,5R,6R)-3-Azatricyclo[4.2.1.02,5]non-7-en-4-one is the starting racemate for 1,4-ethylene-bridged cispentacin.

Technology Process of (1S,2S,5R,6R)-3-AZATRICYCLO[4.2.1.0(2,5)]NON-7-EN-4-ONE

There total 14 articles about (1S,2S,5R,6R)-3-AZATRICYCLO[4.2.1.0(2,5)]NON-7-EN-4-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: 92.0%