(S)-indoline-2-ylmethanol

97%

Reagent Code: #235865
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CAS Number 27640-33-1

science Other reagents with same CAS 27640-33-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 149.2 g/mol
Formula C₉H₁₁NO
badge Registry Numbers
MDL Number MFCD02683225
thermostat Physical Properties
Melting Point 66 - 70 ℃ - lit.
Boiling Point 309.1 ℃ at 760 mmHg
inventory_2 Storage & Handling
Density 1.12 g/cm3
Storage Room temperature

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of biologically active compounds where stereochemistry plays a critical role. Its structure supports the formation of nitrogen-containing heterocycles, making it valuable in drug discovery for central nervous system agents and kinase inhibitors. Commonly employed in asymmetric synthesis to introduce chirality, enhancing the selectivity and potency of target molecules. Also utilized in the preparation of intermediates for natural product synthesis and medicinal chemistry research.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿3,400.00
inventory 1g
10-20 days ฿10,830.00
(S)-indoline-2-ylmethanol
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of biologically active compounds where stereochemistry plays a critical role. Its structure supports the formation of nitrogen-containing heterocycles, making it valuable in drug discovery for central nervous system agents and kinase inhibitors. Commonly employed in asymmetric synthesis to introduce chirality, enhancing the selectivity and potency of target molecules. Also utilized in the preparation of inte
Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of biologically active compounds where stereochemistry plays a critical role. Its structure supports the formation of nitrogen-containing heterocycles, making it valuable in drug discovery for central nervous system agents and kinase inhibitors. Commonly employed in asymmetric synthesis to introduce chirality, enhancing the selectivity and potency of target molecules. Also utilized in the preparation of intermediates for natural product synthesis and medicinal chemistry research.
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