(S)-Methyl (1-aminopropan-2-yl)carbamate hydrochloride

98%

Reagent Code: #236736
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CAS Number 1229025-32-4

science Other reagents with same CAS 1229025-32-4

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inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of β-adrenergic receptor agonists like salbutamol and terbutaline. These drugs are widely used in the treatment of asthma and other respiratory conditions due to their bronchodilator effects. The chiral center in the molecule is crucial for biological activity, making the (S)-enantiomer especially valuable in ensuring high selectivity and efficacy in the final drug product. It is also employed in the preparation of other amine-containing bioactive molecules where a protected amine and a chiral backbone are required.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿720.00
inventory 1g
10-20 days ฿2,700.00
(S)-Methyl (1-aminopropan-2-yl)carbamate hydrochloride
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of β-adrenergic receptor agonists like salbutamol and terbutaline. These drugs are widely used in the treatment of asthma and other respiratory conditions due to their bronchodilator effects. The chiral center in the molecule is crucial for biological activity, making the (S)-enantiomer especially valuable in ensuring high selectivity and efficacy in the final drug product. It is also employed in the preparatio

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of β-adrenergic receptor agonists like salbutamol and terbutaline. These drugs are widely used in the treatment of asthma and other respiratory conditions due to their bronchodilator effects. The chiral center in the molecule is crucial for biological activity, making the (S)-enantiomer especially valuable in ensuring high selectivity and efficacy in the final drug product. It is also employed in the preparation of other amine-containing bioactive molecules where a protected amine and a chiral backbone are required.

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