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61863-41-0

2-[(1S,2S,4S)-BICYCLO[2.2.1]HEPT-5-EN-2-YL]ETHANAMINE

Catalog#: AR00F5OM  |   CAS#: 61863-41-0  |   MDL#: MFCD09864246  |   MF: C9H15N  |   MW: 137.2221

Packsize Purity Price Availability Quantity
50mg 95% $155.00 2-3 weeks Buy Now Add To Cart
100mg 95% $218.00 2-3 weeks Buy Now Add To Cart
250mg 95% $300.00 2-3 weeks Buy Now Add To Cart
500mg 95% $540.00 2-3 weeks Buy Now Add To Cart
1g 95% $712.00 2-3 weeks Buy Now Add To Cart
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Catalog Number AR00F5OM
Chemical Name 2-[(1S,2S,4S)-BICYCLO[2.2.1]HEPT-5-EN-2-YL]ETHANAMINE
CAS Number 61863-41-0
Molecular Formula C9H15N
Molecular Weight 137.2221
MDL Number MFCD09864246
SMILES NCC[C@@H]1C[C@H]2C[C@@H]1C=C2

2-[(1S,2S,4S)-BICYCLO[2.2.1]HEPT-5-EN-2-YL]ETHANAMINE, also known as $name$, is a valuable compound widely utilized in chemical synthesis. Its unique structure, derived from the bicyclic heptane moiety, provides notable reactivity that makes it particularly useful in organic transformations.One key application of 2-[(1S,2S,4S)-BICYCLO[2.2.1]HEPT-5-EN-2-YL]ETHANAMINE is as a versatile building block in the synthesis of pharmaceuticals and agrochemicals. The bicyclic structure lends itself well to forming complex molecules through various synthetic routes, allowing for the efficient production of new compounds with potential biological activities.Furthermore, the presence of the amine functional group in 2-[(1S,2S,4S)-BICYCLO[2.2.1]HEPT-5-EN-2-YL]ETHANAMINE enables it to participate in a range of organic reactions, such as reductive amination, nucleophilic substitution, and transition metal-catalyzed cross-coupling reactions. This reactivity broadens the compound's utility in diverse synthetic sequences, enhancing its value in the chemical synthesis toolkit.
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