4-Chloro-N-[(1,1-dimethylethoxy)carbonyl]-N-methyl-D-phenylalanine

95%

Reagent Code: #166779
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CAS Number 125324-00-7

science Other reagents with same CAS 125324-00-7

blur_circular Chemical Specifications

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Weight 313.78 g/mol
Formula C₁₅H₂₀ClNO₄
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MDL Number MFCD00236864
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of pharmaceutical peptides, particularly in the production of protease inhibitors. Its protected amine group allows for selective coupling reactions in solid-phase peptide synthesis. The chloro-substituent enhances binding specificity in bioactive molecules, making it valuable in developing drugs targeting neurological and metabolic disorders. Commonly employed in research settings for designing enzyme inhibitors with improved stability and activity.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿16,480.00
inventory 1g
10-20 days ฿45,620.00
inventory 50mg
10-20 days ฿5,060.00

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4-Chloro-N-[(1,1-dimethylethoxy)carbonyl]-N-methyl-D-phenylalanine
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Used as an intermediate in the synthesis of pharmaceutical peptides, particularly in the production of protease inhibitors. Its protected amine group allows for selective coupling reactions in solid-phase peptide synthesis. The chloro-substituent enhances binding specificity in bioactive molecules, making it valuable in developing drugs targeting neurological and metabolic disorders. Commonly employed in research settings for designing enzyme inhibitors with improved stability and activity.

Used as an intermediate in the synthesis of pharmaceutical peptides, particularly in the production of protease inhibitors. Its protected amine group allows for selective coupling reactions in solid-phase peptide synthesis. The chloro-substituent enhances binding specificity in bioactive molecules, making it valuable in developing drugs targeting neurological and metabolic disorders. Commonly employed in research settings for designing enzyme inhibitors with improved stability and activity.

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