(S)-(+)-Indoline-2-methanol is a chiral organic compound characterized by its indoline structure, which consists of a fused benzene and pyrrole ring. This compound features a hydroxymethyl group (-CH2OH) at the 2-position of the indoline ring, contributing to its reactivity and potential applications in organic synthesis and pharmaceuticals. The presence of the chiral center allows for the existence of enantiomers, with the (S)-(+)-configuration being the specific enantiomer of interest. This compound is typically a white to off-white solid and is soluble in polar solvents, such as alcohols and water, due to the hydroxyl group. Its unique structure and chirality make it valuable in asymmetric synthesis and as a building block in the development of biologically active molecules. Additionally, (S)-(+)-Indoline-2-methanol may exhibit specific biological activities, making it a subject of interest in medicinal chemistry and drug development. Safety and handling precautions should be observed, as with all chemical substances, to mitigate any potential hazards.

(S)-(+)-Indoline-2-methanol

27640-33-1: (S)-(+)-Indoline-2-methanol is a chiral organic compound characterized by its indoline structure, which consists of a fused benzene and pyrrole ring. This compound features a hydroxymethyl group (-CH2OH) at the 2-position of the indoline ring, contributing to its reactivity and potential applications in organic synthesis and pharmaceuticals. The presence of the chiral center allows for the existence of enantiomers, with the (S)-(+)-configuration being the specific enantiomer of interest. This compound is typically a white to off-white solid and is soluble in polar solvents, such as alcohols and water, due to the hydroxyl group. Its unique structure and chirality make it valuable in asymmetric synthesis and as a building block in the development of biologically active molecules. Additionally, (S)-(+)-Indoline-2-methanol may exhibit specific biological activities, making it a subject of interest in medicinal chemistry and drug development. Safety and handling precautions should be observed, as with all chemical substances, to mitigate any potential hazards.

CAS 27640-33-1

(S)-(+)-Indoline-2-methanol

(S)-(+)-2-Indolinemethanol

Ref: IN-DA002UBD

(S)-(+)-Indoline-2-Methanol

Ref: 54-OR316029

(S)-Indolin-2-ylmethanol

Ref: 10-F445872