(S)-4-(1-Aminoethyl)-2-methoxybenzoic acid hydrochloride

95%

Reagent Code: #235712
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CAS Number 2216747-15-6

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blur_circular Chemical Specifications

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Weight 231.68 g/mol
Formula C₁₀H₁₄ClNO₃
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed from light

description Product Description

Used in the synthesis of β-adrenergic receptor agonists, particularly in the development of bronchodilators for respiratory conditions such as asthma and chronic obstructive pulmonary disease (COPD). Its chiral structure makes it a valuable intermediate in producing enantiomerically pure active pharmaceutical ingredients. Commonly employed in drug manufacturing processes where the (S)-enantiomer contributes to higher biological activity and selectivity. Also utilized in research settings for structure-activity relationship studies of adrenergic drugs.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,410.00
inventory 250mg
10-20 days ฿8,000.00
(S)-4-(1-Aminoethyl)-2-methoxybenzoic acid hydrochloride
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Used in the synthesis of β-adrenergic receptor agonists, particularly in the development of bronchodilators for respiratory conditions such as asthma and chronic obstructive pulmonary disease (COPD). Its chiral structure makes it a valuable intermediate in producing enantiomerically pure active pharmaceutical ingredients. Commonly employed in drug manufacturing processes where the (S)-enantiomer contributes to higher biological activity and selectivity. Also utilized in research settings for structure-activ
Used in the synthesis of β-adrenergic receptor agonists, particularly in the development of bronchodilators for respiratory conditions such as asthma and chronic obstructive pulmonary disease (COPD). Its chiral structure makes it a valuable intermediate in producing enantiomerically pure active pharmaceutical ingredients. Commonly employed in drug manufacturing processes where the (S)-enantiomer contributes to higher biological activity and selectivity. Also utilized in research settings for structure-activity relationship studies of adrenergic drugs.
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