1H-Indole-2-methanol, 2,3-dihydro- is a chemical compound characterized by its indole structure, which consists of a fused benzene and pyrrole ring. This compound features a hydroxymethyl group (-CH2OH) at the 2-position of the indole ring, contributing to its reactivity and potential biological activity. The dihydro designation indicates that the compound has two additional hydrogen atoms, suggesting it is in a saturated form compared to the fully aromatic indole. This saturation can influence its solubility and interaction with biological systems. The presence of the hydroxymethyl group may also enhance its ability to participate in hydrogen bonding, making it a candidate for various chemical reactions and applications in medicinal chemistry. Additionally, compounds with indole structures are often studied for their pharmacological properties, including anti-inflammatory and antimicrobial activities. Overall, 1H-Indole-2-methanol, 2,3-dihydro- is of interest in both synthetic and medicinal chemistry due to its unique structural features and potential therapeutic applications.

1H-Indole-2-methanol, 2,3-dihydro-

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2,3-DIHYDRO-1H-INDOL-2-YLMETHANOL

2-(Hydroxymethyl)indoline

2-(Hydroxymethyl)indoline is an organic compound with the formula C6H11NO. It is a colorless liquid that smells like ammonia. The compound was first synthesized in 1882 by Emil Fischer and was identified as an α-amino acid, which he called "indoline." 2-(Hydroxymethyl)indoline is used to synthesize other compounds and has been shown to react with nitric acid to form 2-nitrosoindoline. This reagent can be used for the synthesis of stereospecific products, such as 1-hydroxy-1,2-dihydroquinolin-2(1H)-one. Recrystallization of this product from ethanol yields 2-(hydroxymethyl)indoline in high purity.

CAS 138969-57-0: 1H-Indole-2-methanol, 2,3-dihydro-

2,3-DIHYDRO-1H-INDOL-2-YLMETHANOL

Ref: 10-F386900

2-(Hydroxymethyl)indoline

Ref: 54-OR14016

1H-Indole-2-methanol, 2,3-dihydro-

Ref: IN-DA0019XZ

2-(Hydroxymethyl)indoline

Ref: 3D-NFA96957