Description
7-Methyl-7-azabicyclo[4.1.0]heptane (CAS No. 51066-08-1) is a highly specialized bicyclic organic compound with the molecular formula C7H13N. This structurally unique molecule features a fused azabicyclo ring system, making it a valuable intermediate in synthetic organic chemistry and pharmaceutical research. The compound is characterized by its high purity and stability under standard laboratory conditions, ensuring reliable performance in demanding applications.
Our product is rigorously tested to meet the highest quality standards, with detailed analytical data (including GC/MS, NMR, and HPLC) available upon request. It is supplied in sealed containers under inert atmosphere to guarantee longevity and prevent degradation. Researchers will appreciate the compound’s versatility as a building block for complex nitrogen-containing heterocycles, particularly in the development of novel bioactive molecules and catalysts.
Storage recommendation: Maintain in a cool, dry environment (2-8°C) under inert gas. Handle with standard laboratory precautions in a well-ventilated area.
Properties
- CAS Number: 51066-08-1
- Complexity: 88.6
- IUPAC Name: 7-methyl-7-azabicyclo[4.1.0]heptane
- InChI: InChI=1S/C7H13N/c1-8-6-4-2-3-5-7(6)8/h6-7H,2-5H2,1H3
- InChI Key: AUKSCMCYMDCFAB-UHFFFAOYSA-N
- Exact Mass: 111.104799419
- Molecular Formula: C7H13N
- Molecular Weight: 111.18
- SMILES: CN1C2C1CCCC2
- Topological: 3
- Monoisotopic Mass: 111.104799419
- Synonyms: 7-Methyl-7-azabicyclo[4.1.0]heptane, 51066-08-1, 7-Azabicyclo[4.1.0]heptane, 7-methyl-, 7-Methyl-7-azabicyclo[4,1,0]heptane, 7-Methyl-7-aza-bicyclo[4.1.0]heptane, MFCD17215407, SCHEMBL8340733, AUKSCMCYMDCFAB-UHFFFAOYSA-N, AKOS015968915, 7-methyl-7-azabicyclo[4.1.0] heptane, DB-333781, CS-0256419, EN300-6486792
Application
7-Methyl-7-azabicyclo[4.1.0]heptane serves as a key synthetic intermediate in medicinal chemistry for the development of nitrogen-rich pharmacophores. Its constrained bicyclic structure makes it particularly valuable for creating rigid molecular scaffolds in drug discovery programs. The compound finds application in asymmetric synthesis as a chiral auxiliary and in materials science for designing novel nitrogen-containing polymers. Researchers also utilize this building block in the synthesis of advanced catalyst systems for organic transformations.
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