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Home  > Spiro[cyclopentane-1,3'-[3H]indol]-2'(1'H)-one, 6'-amino-

AY16498

100510-66-5 | Spiro[cyclopentane-1,3'-[3H]indol]-2'(1'H)-one, 6'-amino-

Packsize Purity Availability Price Discounted Price    Quantity
100mg 96% in stock $479.00 $335.00 -   +
250mg 96% in stock $836.00 $585.00 -   +
1g 96% in stock $2,140.00 $1,498.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AY16498
Chemical Name: Spiro[cyclopentane-1,3'-[3H]indol]-2'(1'H)-one, 6'-amino-
CAS Number: 100510-66-5
Molecular Formula: C12H14N2O
Molecular Weight: 202.2524
MDL Number: MFCD24555999
SMILES: Nc1ccc2c(c1)NC(=O)C12CCCC1

 

Upstream Synthesis Route
  • 6′-Aminospiro[cyclopentane-1,3′-[3H]indol]-2′(1′H)-one is a versatile compound widely used in chemical synthesis due to its unique structure and reactivity. In organic chemistry, this compound serves as a valuable building block in the development of pharmaceuticals, agrochemicals, and materials science.One of the key applications of 6′-Aminospiro[cyclopentane-1,3′-[3H]indol]-2′(1′H)-one is its role as a chiral auxiliary in asymmetric synthesis. By incorporating this compound into a reaction, chemists can control the stereochemistry of the resulting products, enabling the synthesis of enantiomerically pure compounds with high selectivity.Furthermore, 6′-Aminospiro[cyclopentane-1,3′-[3H]indol]-2′(1′H)-one can also participate in various cyclization reactions to form complex ring structures with high efficiency. Its spirocyclic framework imparts rigidity and spatial constraints, making it a valuable tool in the construction of diverse molecular architectures.Overall, the unique structural features and reactivity of 6′-Aminospiro[cyclopentane-1,3′-[3H]indol]-2′(1′H)-one make it an indispensable component in modern synthetic chemistry, facilitating the development of novel compounds with potential applications in drug discovery, materials design, and other areas of chemical research.
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