3-(((tert-Butoxycarbonyl)(methyl)amino)methyl)benzoic acid

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Reagent Code: #130693
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CAS Number 155567-87-6

science Other reagents with same CAS 155567-87-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 265.31 g/mol
Formula C₁₄H₁₉NO₄
badge Registry Numbers
MDL Number MFCD11858334
thermostat Physical Properties
Boiling Point 408.9±34.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.163±0.06 g/cm3(Predicted)
Storage Room temperature, seal, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of protease inhibitors and other bioactive molecules. Its structure allows for selective modifications in peptide-based drug design, making it valuable in medicinal chemistry. The carboxylic acid and protected amine functionalities enable coupling reactions and stepwise assembly of complex molecules, especially in solid-phase and solution-phase peptide synthesis. Commonly employed in research settings for creating libraries of compounds aimed at targeting enzymes involved in metabolic and signaling pathways.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,880.00
inventory 250mg
10-20 days ฿6,580.00
inventory 1g
10-20 days ฿17,740.00

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3-(((tert-Butoxycarbonyl)(methyl)amino)methyl)benzoic acid
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of protease inhibitors and other bioactive molecules. Its structure allows for selective modifications in peptide-based drug design, making it valuable in medicinal chemistry. The carboxylic acid and protected amine functionalities enable coupling reactions and stepwise assembly of complex molecules, especially in solid-phase and solution-phase peptide synthesis. Commonly employed in research settings fo

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of protease inhibitors and other bioactive molecules. Its structure allows for selective modifications in peptide-based drug design, making it valuable in medicinal chemistry. The carboxylic acid and protected amine functionalities enable coupling reactions and stepwise assembly of complex molecules, especially in solid-phase and solution-phase peptide synthesis. Commonly employed in research settings for creating libraries of compounds aimed at targeting enzymes involved in metabolic and signaling pathways.

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