2-(((tert-Butoxycarbonyl)amino)methyl)thiazole-4-carboxylic acid

≥98%

Reagent Code: #130922
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CAS Number 71904-80-8

science Other reagents with same CAS 71904-80-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 258.29 g/mol
Formula C₁₀H₁₄N₂O₄S
badge Registry Numbers
MDL Number MFCD10703327
thermostat Physical Properties
Melting Point 178-179 °C
Boiling Point 438.2±25.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.318±0.06 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of protease inhibitors and other biologically active molecules. Its structure allows for selective modification in peptide-like frameworks, making it valuable in medicinal chemistry for constructing complex heterocyclic systems. Commonly employed in solid-phase and solution-phase peptide synthesis due to the presence of both carboxylic acid and protected amine functionalities. The Boc-protected amine ensures stability during reactions while enabling deprotection for further coupling steps. Frequently utilized in the preparation of drug candidates targeting viral infections and metabolic disorders.

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inventory 1g
10-20 days ฿27,750.00

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2-(((tert-Butoxycarbonyl)amino)methyl)thiazole-4-carboxylic acid
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of protease inhibitors and other biologically active molecules. Its structure allows for selective modification in peptide-like frameworks, making it valuable in medicinal chemistry for constructing complex heterocyclic systems. Commonly employed in solid-phase and solution-phase peptide synthesis due to the presence of both carboxylic acid and protected amine functionalities. The Boc-protected amine ens
Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of protease inhibitors and other biologically active molecules. Its structure allows for selective modification in peptide-like frameworks, making it valuable in medicinal chemistry for constructing complex heterocyclic systems. Commonly employed in solid-phase and solution-phase peptide synthesis due to the presence of both carboxylic acid and protected amine functionalities. The Boc-protected amine ensures stability during reactions while enabling deprotection for further coupling steps. Frequently utilized in the preparation of drug candidates targeting viral infections and metabolic disorders.
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