(S)-2-Isopropylamino-3-methyl-1-butanol

97%

Reagent Code: #234267
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Alias (S)-2-isopropano-3-methyl-1-butanol
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CAS Number 112211-88-8

science Other reagents with same CAS 112211-88-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 145.24 g/mol
Formula C₈H₁₉NO
inventory_2 Storage & Handling
Density 0.88
Storage Room temperature

description Product Description

Used primarily as an intermediate in the synthesis of β-adrenergic receptor agonists, particularly in the production of bronchodilators for treating respiratory conditions such as asthma and chronic obstructive pulmonary disease (COPD). Its chiral structure makes it valuable in asymmetric synthesis, where stereochemistry is critical for the biological activity of the final pharmaceutical product. It is also employed in the development of cardiovascular drugs due to its structural similarity to adrenergic agents. The compound's hydroxyl and amine functional groups allow for versatile chemical modifications, facilitating its incorporation into more complex drug molecules.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿3,730.00
(S)-2-Isopropylamino-3-methyl-1-butanol
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Used primarily as an intermediate in the synthesis of β-adrenergic receptor agonists, particularly in the production of bronchodilators for treating respiratory conditions such as asthma and chronic obstructive pulmonary disease (COPD). Its chiral structure makes it valuable in asymmetric synthesis, where stereochemistry is critical for the biological activity of the final pharmaceutical product. It is also employed in the development of cardiovascular drugs due to its structural similarity to adrenergic

Used primarily as an intermediate in the synthesis of β-adrenergic receptor agonists, particularly in the production of bronchodilators for treating respiratory conditions such as asthma and chronic obstructive pulmonary disease (COPD). Its chiral structure makes it valuable in asymmetric synthesis, where stereochemistry is critical for the biological activity of the final pharmaceutical product. It is also employed in the development of cardiovascular drugs due to its structural similarity to adrenergic agents. The compound's hydroxyl and amine functional groups allow for versatile chemical modifications, facilitating its incorporation into more complex drug molecules.

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