Methyl (S)-3-amino-3-(furan-2-yl)propanoate hydrochloride

95%

Reagent Code: #233377
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CAS Number 2703745-98-4

science Other reagents with same CAS 2703745-98-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 205.64 g/mol
Formula C₈H₁₂ClNO₃
badge Registry Numbers
MDL Number MFCD24422792
inventory_2 Storage & Handling
Storage 2-8°C, Sealed, Inert Gas

description Product Description

Used as a chiral building block in the synthesis of biologically active compounds, particularly in pharmaceuticals targeting neurological and cardiovascular diseases. Its furan ring and amine functionality make it valuable for constructing enzyme inhibitors and receptor ligands. Commonly employed in asymmetric synthesis to introduce stereochemistry in drug candidates. Also utilized in the preparation of beta-amino acid derivatives, which are important in peptidomimetic design for improved metabolic stability.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿23,060.00
inventory 1g
10-20 days ฿86,220.00
inventory 250mg
10-20 days ฿34,610.00
Methyl (S)-3-amino-3-(furan-2-yl)propanoate hydrochloride
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Used as a chiral building block in the synthesis of biologically active compounds, particularly in pharmaceuticals targeting neurological and cardiovascular diseases. Its furan ring and amine functionality make it valuable for constructing enzyme inhibitors and receptor ligands. Commonly employed in asymmetric synthesis to introduce stereochemistry in drug candidates. Also utilized in the preparation of beta-amino acid derivatives, which are important in peptidomimetic design for improved metabolic stabi

Used as a chiral building block in the synthesis of biologically active compounds, particularly in pharmaceuticals targeting neurological and cardiovascular diseases. Its furan ring and amine functionality make it valuable for constructing enzyme inhibitors and receptor ligands. Commonly employed in asymmetric synthesis to introduce stereochemistry in drug candidates. Also utilized in the preparation of beta-amino acid derivatives, which are important in peptidomimetic design for improved metabolic stability.

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