(R)-2-Amino-2-(3-methoxyphenyl)ethanol

98%

Reagent Code: #37552
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CAS Number 763080-04-2

science Other reagents with same CAS 763080-04-2

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Weight 167.2100 g/mol
Formula C₉H₁₃NO₂
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Storage room temperature

description Product Description

This compound is primarily utilized in the synthesis of pharmaceuticals, particularly as an intermediate in the production of active pharmaceutical ingredients (APIs). Its chiral structure makes it valuable in the development of enantiomerically pure drugs, which are crucial for ensuring specificity and reducing side effects in therapeutic applications. It is often employed in the creation of beta-adrenergic receptor agonists, which are used to treat conditions such as asthma and cardiovascular diseases. Additionally, its methoxy and amino functional groups allow for further chemical modifications, enabling its use in the design of complex molecules with targeted biological activities.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿10,062.00

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(R)-2-Amino-2-(3-methoxyphenyl)ethanol
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This compound is primarily utilized in the synthesis of pharmaceuticals, particularly as an intermediate in the production of active pharmaceutical ingredients (APIs). Its chiral structure makes it valuable in the development of enantiomerically pure drugs, which are crucial for ensuring specificity and reducing side effects in therapeutic applications. It is often employed in the creation of beta-adrenergic receptor agonists, which are used to treat conditions such as asthma and cardiovascular diseases.

This compound is primarily utilized in the synthesis of pharmaceuticals, particularly as an intermediate in the production of active pharmaceutical ingredients (APIs). Its chiral structure makes it valuable in the development of enantiomerically pure drugs, which are crucial for ensuring specificity and reducing side effects in therapeutic applications. It is often employed in the creation of beta-adrenergic receptor agonists, which are used to treat conditions such as asthma and cardiovascular diseases. Additionally, its methoxy and amino functional groups allow for further chemical modifications, enabling its use in the design of complex molecules with targeted biological activities.

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