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MSE PRO 2-Azabicyclo[2.2.1]heptan-3-one, ≥99.0% Purity– MSE Supplies LLC

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MSE PRO 2-Azabicyclo[2.2.1]heptan-3-one, ≥99.0% Purity - MSE Supplies LLC

MSE PRO 2-Azabicyclo[2.2.1]heptan-3-one, ≥99.0% Purity

SKU: CM1355

  • $ 47995

MSE PRO™ 2-Azabicyclo[2.2.1]heptan-3-one, ≥99.0% Purity

MSE PRO™ 2-Azabicyclo[2.2.1]heptan-3-one is a chemical compound with a bicyclic structure containing a nitrogen atom within the ring system. The bicyclic structure of 2-azabicyclo[2.2.1]heptan-3-one imparts unique reactivity characteristics, making it valuable in organic synthesis. The presence of the lactam functionality provides a site for nucleophilic attack, allowing for the formation of various derivatives through chemical transformations. Pyrrolidine-3-one derivatives exhibit pharmacological activities and are utilized in the synthesis of pharmaceutical agents. They serve as key structural motifs in many biologically active compounds, including drugs targeting receptors, enzymes, and ion channels.

MSE Supplies offers various N-heterocyclic drug small molecules. Please contact us for bulk orders.

Technical Specifications:

CAS No. 24647-29-8
Chemical name 2-Azabicyclo[2.2.1]heptan-3-one
Synonym(s)

  • 2-Azanorbornan-3-one

  • 3-azabicyclo[2.2.1]heptan-2-one
Molecular formula C6H9NO
Pack size

1 g (CM1355);5 g (CM1356)
Molecular weight 111.14 g/mol
Melting point  69-74 ℃
Density  1.137 g/mL 
Purity 99.97% (GC)
pKa
 		16.63±0.20 (Predicted)
Appearance Off-white to light yellow solid
Storage  Store at room temperature


References:

[1] Singh, R., & Vince, R. (2012). 2-Azabicyclo [2.2. 1] hept-5-en-3-one: chemical profile of a versatile synthetic building block and its impact on the development of therapeutics. Chemical Reviews, 112(8), 4642-4686.

[2] Palmer, C. F., Parry, K. P., Roberts, S. M., & Sik, V. (1991). Chemistry of 2-azabicyclo [2.2. 1] heptan-3-one derivatives: role of the nitrogen atom in determining the stereochemistry of products isolated after formation of an incipient carbocation at C-6. Journal of the Chemical Society, Perkin Transactions 1, (8), 2051-2052.