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59213-02-4

3-(3-Formyl-1H-indol-1-yl)propanoic acid

Catalog#: AR00EEQP  |   CAS#: 59213-02-4  |   MDL#: MFCD00484156  |   MF: C12H11NO3  |   MW: 217.2206

Packsize Purity Price Availability Quantity
50mg 95% $65.00 2-3 weeks Buy Now Add To Cart
100mg 95% $86.00 2-3 weeks Buy Now Add To Cart
250mg 95% $111.00 2-3 weeks Buy Now Add To Cart
500mg 95% $162.00 2-3 weeks Buy Now Add To Cart
1g 95% $199.00 2-3 weeks Buy Now Add To Cart
2.5g 95% $244.00 2-3 weeks Buy Now Add To Cart
5g 95% $318.00 2-3 weeks Buy Now Add To Cart
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Catalog Number AR00EEQP
Chemical Name 3-(3-Formyl-1H-indol-1-yl)propanoic acid
CAS Number 59213-02-4
Molecular Formula C12H11NO3
Molecular Weight 217.2206
MDL Number MFCD00484156
SMILES O=Cc1cn(c2c1cccc2)CCC(=O)O

3-(3-Formyl-1H-indol-1-yl)propanoic acid is a versatile compound commonly used in chemical synthesis as a key intermediate in organic reactions. Its application in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals is particularly noteworthy due to its unique structure and reactivity. This compound serves as a crucial building block in the production of various functionalized molecules, enabling the creation of complex structures with diverse applications.In chemical synthesis, 3-(3-Formyl-1H-indol-1-yl)propanoic acid plays a pivotal role in the formation of heterocyclic compounds, which are essential in drug discovery and development. By incorporating this compound into synthetic pathways, chemists can introduce specific functional groups and stereochemical features that are vital for enhancing the biological activity and properties of the final products. Furthermore, the presence of the formyl group in the molecule offers opportunities for selective chemical transformations, such as reduction or condensation reactions, leading to the generation of structurally diverse compounds with tailored properties.Moreover, the indole moiety in 3-(3-Formyl-1H-indol-1-yl)propanoic acid imparts distinct aromatic and electron-rich properties, making it a valuable component in the construction of conjugated systems and π-extended structures. This enables the development of molecules with enhanced optical and electronic properties, which are essential in materials science and organic electronics. Additionally, the presence of a propanoic acid functional group provides a handle for further derivatization, allowing for the introduction of additional functionalities or modifications to fine-tune the properties of the synthesized compounds.Overall, the strategic use of 3-(3-Formyl-1H-indol-1-yl)propanoic acid in chemical synthesis offers chemists a powerful tool for the design and preparation of structurally diverse and functionally rich compounds with applications spanning the fields of drug discovery, materials science, and agrochemical development.
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GHS Pictogram N/A
UN# -
Hazard Statements -
Class -
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