3-(BOC-AMINO)BENZOIC ACID

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Reagent Code: #144652
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CAS Number 111331-82-9

science Other reagents with same CAS 111331-82-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 237.25 g/mol
Formula C₁₂H₁₅NO₄
badge Registry Numbers
MDL Number MFCD00235884
thermostat Physical Properties
Melting Point 195°C dec.
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals and bioactive molecules, particularly in peptide chemistry and drug development. The BOC-protected amine group allows for controlled deprotection during stepwise synthesis, making it valuable in solid-phase and solution-phase peptide coupling. Its carboxylic acid functionality enables attachment to other molecular scaffolds through amide or ester bond formation. Commonly employed in the preparation of protease inhibitors, receptor agonists, and targeted therapeutics where precise functional group manipulation is required. Also utilized in the development of labeled compounds for biochemical assays due to its stability and selective reactivity.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿168.00
inventory 5g
10-20 days ฿360.00
inventory 25g
10-20 days ฿1,400.00
inventory 100g
10-20 days ฿5,570.00
inventory 500g
10-20 days ฿27,830.00

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3-(BOC-AMINO)BENZOIC ACID
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Used as a key intermediate in the synthesis of pharmaceuticals and bioactive molecules, particularly in peptide chemistry and drug development. The BOC-protected amine group allows for controlled deprotection during stepwise synthesis, making it valuable in solid-phase and solution-phase peptide coupling. Its carboxylic acid functionality enables attachment to other molecular scaffolds through amide or ester bond formation. Commonly employed in the preparation of protease inhibitors, receptor agonists, a

Used as a key intermediate in the synthesis of pharmaceuticals and bioactive molecules, particularly in peptide chemistry and drug development. The BOC-protected amine group allows for controlled deprotection during stepwise synthesis, making it valuable in solid-phase and solution-phase peptide coupling. Its carboxylic acid functionality enables attachment to other molecular scaffolds through amide or ester bond formation. Commonly employed in the preparation of protease inhibitors, receptor agonists, and targeted therapeutics where precise functional group manipulation is required. Also utilized in the development of labeled compounds for biochemical assays due to its stability and selective reactivity.

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