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14651-42-4

Tricyclo[3.3.1.13,7]decane, 1-(bromomethyl)-

Catalog#: AR001ERS  |   CAS#: 14651-42-4  |   MDL#: MFCD00185303  |   MF: C11H17Br  |   MW: 229.1567

Packsize Purity Price Availability Quantity
100mg 98% $5.00 Global Stock Buy Now Add To Cart
250mg 98% $6.00 Global Stock Buy Now Add To Cart
1g 98% $19.00 Global Stock Buy Now Add To Cart
5g 98% $72.00 Global Stock Buy Now Add To Cart
10g 98% $142.00 Global Stock Buy Now Add To Cart
25g 98% $347.00 Global Stock Buy Now Add To Cart
50g 98% $554.00 Global Stock Buy Now Add To Cart
100g 98% $1,039.00 Global Stock Buy Now Add To Cart
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Catalog Number AR001ERS
Chemical Name Tricyclo[3.3.1.13,7]decane, 1-(bromomethyl)-
CAS Number 14651-42-4
Molecular Formula C11H17Br
Molecular Weight 229.1567
MDL Number MFCD00185303
SMILES BrCC12CC3CC(C2)CC(C1)C3

1-(Bromomethyl)adamantane is a versatile compound widely used in organic chemical synthesis due to its unique structure and reactivity. It serves as an important building block in the construction of complex organic molecules and has various applications in the field of medicinal chemistry, materials science, and drug development.As a reactive brominated compound, 1-(Bromomethyl)adamantane undergoes various substitution and elimination reactions, making it a valuable intermediate in the synthesis of pharmaceuticals, agrochemicals, and functional materials. Its adamantane backbone provides rigidity and steric hindrance, influencing the regioselectivity and stereochemistry of reactions in which it participates.In drug discovery and development, 1-(Bromomethyl)adamantane can be used to introduce the adamantane moiety into bioactive compounds, enhancing their pharmacological properties such as increased lipophilicity and metabolic stability. Its reactivity under different reaction conditions enables the selective modification of specific functional groups within a molecule, leading to the creation of novel compounds with improved biological activities or physical properties.Furthermore, the presence of the bromomethyl group in 1-(Bromomethyl)adamantane allows for further derivatization through cross-coupling reactions, nucleophilic substitutions, and radical reactions, expanding its utility in the synthesis of diverse chemical entities. Its strategic placement of the bromine atom facilitates the introduction of other functionalities or chiral centers, enabling the creation of complex molecular architectures with high synthetic efficiency.Overall, 1-(Bromomethyl)adamantane is a valuable tool in the hands of synthetic chemists, providing a gateway to the development of innovative compounds with potential applications across various scientific disciplines. Its versatility and unique structural features make it a key component in the toolkit of organic chemists seeking to explore new frontiers in chemical synthesis and molecular design.
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GHS Pictogram
Signal Word Warning
UN# N/A
Hazard Statements H302
Precautionary Statements P280-P305+P351+P338
Class N/A
Packing Group N/A

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