N-Chloroacetyl-D-phenylalanine

95%

Reagent Code: #219702
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CAS Number 137503-97-0

science Other reagents with same CAS 137503-97-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 241.67 g/mol
Formula C₁₁H₁₂ClNO₃
badge Registry Numbers
MDL Number MFCD00063159
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used primarily as an intermediate in the synthesis of pharmaceuticals, particularly in the production of certain antibiotics and peptide-based drugs. Its chloroacetyl group allows for selective alkylation reactions, making it valuable in modifying amino acid structures for drug design. It is also employed in the preparation of chiral building blocks for asymmetric synthesis, where the D-phenylalanine backbone contributes to stereochemical control. Additionally, it finds use in research settings for labeling or cross-linking biomolecules due to the reactivity of the chloroacetyl moiety with nucleophiles like thiols.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,520.00
inventory 1g
10-20 days ฿4,050.00
inventory 5g
10-20 days ฿16,320.00
inventory 10g
10-20 days ฿29,670.00
N-Chloroacetyl-D-phenylalanine
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Used primarily as an intermediate in the synthesis of pharmaceuticals, particularly in the production of certain antibiotics and peptide-based drugs. Its chloroacetyl group allows for selective alkylation reactions, making it valuable in modifying amino acid structures for drug design. It is also employed in the preparation of chiral building blocks for asymmetric synthesis, where the D-phenylalanine backbone contributes to stereochemical control. Additionally, it finds use in research settings for label

Used primarily as an intermediate in the synthesis of pharmaceuticals, particularly in the production of certain antibiotics and peptide-based drugs. Its chloroacetyl group allows for selective alkylation reactions, making it valuable in modifying amino acid structures for drug design. It is also employed in the preparation of chiral building blocks for asymmetric synthesis, where the D-phenylalanine backbone contributes to stereochemical control. Additionally, it finds use in research settings for labeling or cross-linking biomolecules due to the reactivity of the chloroacetyl moiety with nucleophiles like thiols.

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