(S)-()-1-Indanol
97%
Reagent
Code: #84850
Alias
(S)-(+)-1-Hydroxyindane
CAS Number
25501-32-0
blur_circular Chemical Specifications
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Molecular Information
Weight
134.18 g/mol
Formula
C₉H₁₀O
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Registry Numbers
MDL Number
MFCD00064165
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Physical Properties
Melting Point
69-73°C (lit.)
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Storage & Handling
Storage
room temperature
description Product Description
(S)-()-1-Indanol is widely used in the pharmaceutical industry as a chiral building block for the synthesis of various drugs. Its enantiomeric purity makes it valuable in the production of compounds with specific stereochemistry, which is crucial for the efficacy and safety of many medications. Additionally, it serves as an intermediate in the synthesis of complex organic molecules, particularly in the development of active pharmaceutical ingredients (APIs) for treating neurological and cardiovascular diseases. In research, it is employed as a reagent or precursor in asymmetric synthesis, aiding in the study of chiral catalysts and enantioselective reactions. Its applications also extend to material science, where it is used in the development of chiral polymers and advanced materials with specific optical properties.
format_list_bulleted Product Specification
Test Parameter | Specification |
---|---|
Appearance | White to off-white solid |
Purity | 96.5-100 |
Infrared Spectrum | Conforms to Structure |
NMR | Conforms to Structure |
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(S)-()-1-Indanol
(S)-()-1-Indanol is widely used in the pharmaceutical industry as a chiral building block for the synthesis of various drugs. Its enantiomeric purity makes it valuable in the production of compounds with specific stereochemistry, which is crucial for the efficacy and safety of many medications. Additionally, it serves as an intermediate in the synthesis of complex organic molecules, particularly in the development of active pharmaceutical ingredients (APIs) for treating neurological and cardiovascular diseases. In research, it is employed as a reagent or precursor in asymmetric synthesis, aiding in the study of chiral catalysts and enantioselective reactions. Its applications also extend to material science, where it is used in the development of chiral polymers and advanced materials with specific optical properties.
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