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CAS 163061-73-2

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(1R,2R)-(-)-TRANS-1-AMINO-2-INDANOL

Description:
(1R,2R)-(-)-TRANS-1-AMINO-2-INDANOL is a chiral compound characterized by its specific stereochemistry, denoted by the (1R,2R) configuration. This substance features an indanol structure, which combines an indole moiety with an alcohol functional group, contributing to its unique chemical properties. The presence of the amino group enhances its potential for forming hydrogen bonds, making it a candidate for various biological interactions. This compound is often studied in the context of medicinal chemistry due to its potential applications in drug development, particularly in the synthesis of pharmaceuticals that target specific biological pathways. Its chirality is significant, as enantiomers can exhibit different biological activities, making the (1R,2R) form particularly relevant in the design of selective agents. Additionally, the trans configuration indicates that the substituents on the indanol ring are oriented in a specific spatial arrangement, which can influence the compound's reactivity and interaction with biological systems. Overall, (1R,2R)-(-)-TRANS-1-AMINO-2-INDANOL is a compound of interest in both synthetic and medicinal chemistry.
Formula:C9H11NO
InChI:InChI=1/C9H11NO/c10-9-7-4-2-1-3-6(7)5-8(9)11/h1-4,8-9,11H,5,10H2/t8-,9-/m1/s1
SMILES:c1ccc2c(c1)C[C@H]([C@@H]2N)O
Synonyms:
  • (1R,2R)-1-Amino-2,3-Dihydro-1H-Inden-2-Ol
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