AW19648
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
50mg | 95% | 1 week | $569.00 | $398.00 | - + | |
100mg | 95% | 1 week | $808.00 | $566.00 | - + | |
250mg | 95% | 1 week | $1,122.00 | $786.00 | - + | |
500mg | 95% | 1 week | $1,722.00 | $1,205.00 | - + | |
1g | 95% | 1 week | $2,186.00 | $1,530.00 | - + | |
2.5g | 95% | 1 week | $4,206.00 | $2,945.00 | - + | |
5g | 95% | 1 week | $6,183.00 | $4,328.00 | - + |
*All products are for research use only and not intended for human or animal use.
*All prices are in USD.
Catalog Number: | AW19648 |
Chemical Name: | 2-(Bromomethyl)spiro[3.3]heptane |
CAS Number: | 102115-83-3 |
Molecular Formula: | C8H13Br |
Molecular Weight: | 189.0928 |
MDL Number: | MFCD20633953 |
SMILES: | BrCC1CC2(C1)CCC2 |
2-(Bromomethyl)spiro[3.3]heptane is a highly versatile compound that finds significant utility in chemical synthesis processes. This compound serves as a valuable building block in the creation of various complex organic molecules, due to its unique structural characteristics and reactivity.In chemical synthesis, 2-(Bromomethyl)spiro[3.3]heptane acts as a key intermediate for the synthesis of spirocyclic compounds. The spirocyclic motif, characterized by two or more rings that share a single common atom, is prevalent in many biologically active molecules and natural products. By incorporating 2-(Bromomethyl)spiro[3.3]heptane into a synthetic pathway, chemists can efficiently access a diverse array of spirocyclic structures, enabling the creation of novel compounds with potential pharmaceutical or biological activities.Furthermore, the bromomethyl group present in 2-(Bromomethyl)spiro[3.3]heptane offers a versatile functional handle for further chemical transformations. This allows for the introduction of additional functional groups or modifications, expanding the scope of synthetic possibilities and enabling the synthesis of more complex molecules.Overall, 2-(Bromomethyl)spiro[3.3]heptane plays a crucial role in chemical synthesis by facilitating the construction of diverse spirocyclic compounds with unique structural and potentially valuable properties.