2-Amino-3-(3-chloro-2-fluorophenyl)propanoic acid hydrochloride

98%

Reagent Code: #138537
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CAS Number 2416231-06-4

science Other reagents with same CAS 2416231-06-4

blur_circular Chemical Specifications

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Weight 254.09 g/mol
Formula C₉H₁₀Cl₂FNO₂
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used as a key intermediate in the synthesis of certain pharmaceutical agents, particularly in the development of antidiabetic drugs such as DPP-4 inhibitors. Its chiral structure and functional groups allow for selective binding and improved metabolic stability in active compounds. Commonly employed in research settings for designing enzyme inhibitors and bioactive molecules. Also utilized in asymmetric synthesis due to its amino acid backbone, enabling the construction of complex organic molecules with high stereochemical control.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿10,810.00
inventory 250mg
10-20 days ฿16,210.00
inventory 1g
10-20 days ฿43,880.00

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2-Amino-3-(3-chloro-2-fluorophenyl)propanoic acid hydrochloride
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Used as a key intermediate in the synthesis of certain pharmaceutical agents, particularly in the development of antidiabetic drugs such as DPP-4 inhibitors. Its chiral structure and functional groups allow for selective binding and improved metabolic stability in active compounds. Commonly employed in research settings for designing enzyme inhibitors and bioactive molecules. Also utilized in asymmetric synthesis due to its amino acid backbone, enabling the construction of complex organic molecules with

Used as a key intermediate in the synthesis of certain pharmaceutical agents, particularly in the development of antidiabetic drugs such as DPP-4 inhibitors. Its chiral structure and functional groups allow for selective binding and improved metabolic stability in active compounds. Commonly employed in research settings for designing enzyme inhibitors and bioactive molecules. Also utilized in asymmetric synthesis due to its amino acid backbone, enabling the construction of complex organic molecules with high stereochemical control.

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