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6134-53-8

4-Bromo-2,3-dihydro-1H-indene

Catalog#: AR0039AL  |   CAS#: 6134-53-8  |   MDL#: MFCD22059711  |   MF: C9H9Br  |   MW: 197.0718

Packsize Purity Price Availability Quantity
100mg 97% $22.00 Global Stock Buy Now Add To Cart
250mg 97% $32.00 Global Stock Buy Now Add To Cart
500mg 97% $42.00 Global Stock Buy Now Add To Cart
1g 97% $61.00 Global Stock Buy Now Add To Cart
5g 97% $205.00 Global Stock Buy Now Add To Cart
10g 97% $369.00 Global Stock Buy Now Add To Cart
25g 97% $715.00 Global Stock Buy Now Add To Cart
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Catalog Number AR0039AL
Chemical Name 4-Bromo-2,3-dihydro-1H-indene
CAS Number 6134-53-8
Molecular Formula C9H9Br
Molecular Weight 197.0718
MDL Number MFCD22059711
SMILES Brc1cccc2c1CCC2

4-Bromo-2,3-dihydro-1H-indene is a versatile intermediate compound widely used in chemical synthesis. Due to its unique structure and reactivity, this compound plays a crucial role in various organic transformations and the synthesis of complex molecules. In particular, 4-Bromo-2,3-dihydro-1H-indene is commonly employed as a key building block in the preparation of biologically active compounds, pharmaceuticals, agrochemicals, and materials.One of the primary applications of 4-Bromo-2,3-dihydro-1H-indene is its contribution to the construction of indene derivatives, which possess important pharmacological properties. The bromo group in this compound serves as a versatile handle for further functionalization, enabling the introduction of various substituents and modifications to fine-tune the properties of the final products. Through appropriate synthetic strategies, chemists can leverage the unique reactivity of 4-Bromo-2,3-dihydro-1H-indene to access diverse molecular scaffolds with enhanced biological activities.Additionally, 4-Bromo-2,3-dihydro-1H-indene can participate in key synthetic transformations such as cross-coupling reactions, cyclization processes, and other bond-forming reactions. These chemical reactions enable the incorporation of the 4-Bromo-2,3-dihydro-1H-indene moiety into more complex molecules, facilitating the preparation of advanced intermediates and target compounds with specific functionalities and structural motifs. By judiciously selecting reaction conditions and substrates, chemists can harness the synthetic potential of 4-Bromo-2,3-dihydro-1H-indene to streamline the synthesis of valuable compounds for various applications in medicinal chemistry, materials science, and beyond.
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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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