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75629-57-1

1-(4-Chlorobenzyl)-1H-indole-3-carbaldehyde

Catalog#: AR008QG6  |   CAS#: 75629-57-1  |   MDL#: MFCD01051808  |   MF: C16H12ClNO  |   MW: 269.7256

Packsize Purity Price Availability Quantity
10mg 95% $38.00 Global Stock Buy Now Add To Cart
50mg 95% $157.00 Global Stock Buy Now Add To Cart
100mg 95% $281.00 Global Stock Buy Now Add To Cart
250mg 95% $556.00 Global Stock Buy Now Add To Cart
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Catalog Number AR008QG6
Chemical Name 1-(4-Chlorobenzyl)-1H-indole-3-carbaldehyde
CAS Number 75629-57-1
Molecular Formula C16H12ClNO
Molecular Weight 269.7256
MDL Number MFCD01051808
SMILES O=Cc1cn(c2c1cccc2)Cc1ccc(cc1)Cl

1-(4-Chlorobenzyl)-1H-indole-3-carbaldehyde is a versatile compound commonly used in chemical synthesis for its unique reactivity and structural properties. This compound serves as a key intermediate in the synthesis of various pharmaceuticals, organic materials, and fine chemicals. Due to the presence of the chlorobenzyl group and the indole ring system, 1-(4-Chlorobenzyl)-1H-indole-3-carbaldehyde undergoes a variety of reactions that allow for the introduction of different functional groups at specific positions. It can be used as a key building block to create complex molecular structures, such as indole derivatives, heterocyclic compounds, and biologically active molecules.In organic synthesis, the aldehyde group of 1-(4-Chlorobenzyl)-1H-indole-3-carbaldehyde acts as a versatile starting point for various transformations, including formation of carbon-carbon bonds through aldol condensation reactions, as well as nucleophilic addition reactions. Additionally, the indole ring confers unique aromatic and electronic properties that can be exploited in the design of new compounds with desired activities or physical properties.Overall, the strategic placement of functional groups in 1-(4-Chlorobenzyl)-1H-indole-3-carbaldehyde provides synthetic chemists with a valuable tool for constructing diverse molecular architectures and advancing the field of chemical synthesis.
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