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7417-65-4

1H-Indole-3-propanoicacid,-alpha--hydroxy-,(-alpha-S)-(9CI)

Catalog#: AR00FDLO  |   CAS#: 7417-65-4  |   MDL#: MFCD09839710  |   MF: C11H11NO3  |   MW: 205.2099

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Catalog Number AR00FDLO
Chemical Name 1H-Indole-3-propanoicacid,-alpha--hydroxy-,(-alpha-S)-(9CI)
CAS Number 7417-65-4
Molecular Formula C11H11NO3
Molecular Weight 205.2099
MDL Number MFCD09839710
SMILES OC(=O)[C@H](Cc1c[nH]c2c1cccc2)O

L-Indole-3-lactic acid is a versatile compound widely utilized in chemical synthesis due to its unique properties and reactivity. With a structure containing both an indole ring and a lactic acid moiety, this compound offers a range of applications in organic chemistry.One of the primary uses of L-Indole-3-lactic acid is as a building block in the synthesis of complex molecules. Its indole ring can undergo various functionalization reactions, allowing for the introduction of different chemical groups and the creation of diverse structures. This versatility makes it a valuable intermediate in the production of pharmaceuticals, agrochemicals, and materials with specific properties.Furthermore, L-Indole-3-lactic acid can serve as a chiral auxiliary in asymmetric synthesis. Its chiral nature, as a result of the lactic acid unit, enables the creation of enantiomerically pure compounds. By utilizing this compound in asymmetric transformations, chemists can access enantiomerically enriched products with high selectivity and efficiency.Additionally, L-Indole-3-lactic acid can act as a ligand in coordination chemistry, forming complexes with various metal ions. These complexes exhibit unique reactivity and catalytic properties, making them valuable in a variety of chemical transformations.Overall, the application of L-Indole-3-lactic acid in chemical synthesis spans a wide range of fields, showcasing its importance as a versatile building block and chiral auxiliary in the creation of diverse molecular structures.
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