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Catalog Number:
16551
CAS Number:
27640-33-1
S -2-indolil metanol
Purity:
≥ 98 % (HPLC)
Synonym(s):
( S -2-(Hidroximetil)indolina
Documents
$72.31 /100 mg
Tamaño
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Product Information

(S)-2-Indolinemethanol is a versatile compound with significant applications in the fields of pharmaceuticals and organic synthesis. This chiral alcohol features a unique indole structure, making it a valuable building block for the synthesis of various bioactive molecules. Its ability to act as a chiral auxiliary allows researchers to enhance the enantioselectivity of reactions, which is crucial in the development of new drugs. The compound's properties lend themselves well to applications in medicinal chemistry, particularly in the design of novel therapeutic agents targeting neurological disorders and cancer.

In addition to its pharmaceutical relevance, (S)-2-Indolinemethanol is also utilized in the production of agrochemicals and fine chemicals, where its indole framework contributes to the efficacy of various formulations. Researchers appreciate its stability and ease of handling, which facilitate its incorporation into complex synthetic pathways. With its broad applicability and potential for innovation, (S)-2-Indolinemethanol stands out as a key compound for professionals seeking to advance their projects in drug discovery and chemical synthesis.

Synonyms
( S -2-(Hidroximetil)indolina
CAS Number
27640-33-1
Purity
≥ 98 % (HPLC)
Molecular Formula
C 9 H 11 NO
Molecular Weight
149.19
MDL Number
MFCD02683225
PubChem ID
2794664
Appearance
Polvo cristalino de color blanco a marrón.
Optical Rotation
[a] D 22 = +52 ± 3º (C=1 en EtOH)
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
( S -2-(Hidroximetil)indolina
CAS Number
27640-33-1
Purity
≥ 98 % (HPLC)
Molecular Formula
C 9 H 11 NO
Molecular Weight
149.19
MDL Number
MFCD02683225
PubChem ID
2794664
Appearance
Polvo cristalino de color blanco a marrón.
Optical Rotation
[a] D 22 = +52 ± 3º (C=1 en EtOH)
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

(S)-2-Indolinemethanol is widely utilized in research focused on

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly those targeting neurological disorders, due to its ability to interact with specific receptors in the brain.
  • Biological Research: Researchers use (S)-2-Indolinemethanol to study its effects on cellular processes, helping to uncover mechanisms of action in cell signaling pathways and potential therapeutic targets.
  • Organic Synthesis: It is employed in organic chemistry as a building block for creating more complex molecules, offering a versatile approach to developing new compounds with desired biological activities.
  • Material Science: The compound is explored for its potential applications in creating novel materials, particularly in the development of sensors and electronic devices, due to its unique electronic properties.
  • Natural Product Synthesis: (S)-2-Indolinemethanol is used in the synthesis of natural products, which can lead to the discovery of new drugs and agrochemicals, providing an edge over similar compounds in terms of efficacy and specificity.

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