(S)-Ethyl 3-aminobutanoate hydrochloride

95%

Reagent Code: #235671
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CAS Number 187876-47-7

science Other reagents with same CAS 187876-47-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 167.63 g/mol
Formula C₆H₁₄ClNO₂
badge Registry Numbers
MDL Number MFCD01862144
inventory_2 Storage & Handling
Storage 2-8°C, stored in inert gas

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the production of beta-amino acid derivatives and bioactive molecules. Its enantiomerically pure structure makes it valuable in asymmetric synthesis, where it helps introduce stereochemical control in drug development. Commonly employed in the preparation of protease inhibitors and other therapeutic agents requiring specific stereochemistry for activity. Also utilized in the development of agrochemicals and specialty chemicals where chirality impacts efficacy.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿630.00
inventory 250mg
10-20 days ฿1,160.00
inventory 1g
10-20 days ฿4,350.00
inventory 5g
10-20 days ฿16,800.00
(S)-Ethyl 3-aminobutanoate hydrochloride
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the production of beta-amino acid derivatives and bioactive molecules. Its enantiomerically pure structure makes it valuable in asymmetric synthesis, where it helps introduce stereochemical control in drug development. Commonly employed in the preparation of protease inhibitors and other therapeutic agents requiring specific stereochemistry for activity. Also utilized in the development of agrochemicals and specialty che

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the production of beta-amino acid derivatives and bioactive molecules. Its enantiomerically pure structure makes it valuable in asymmetric synthesis, where it helps introduce stereochemical control in drug development. Commonly employed in the preparation of protease inhibitors and other therapeutic agents requiring specific stereochemistry for activity. Also utilized in the development of agrochemicals and specialty chemicals where chirality impacts efficacy.

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