Methyl4-((tert-butoxycarbonyl)amino)thiophene-3-carboxylate

97%

Reagent Code: #214159
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CAS Number 161940-20-1

science Other reagents with same CAS 161940-20-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 257.31 g/mol
Formula C₁₁H₁₅NO₄S
badge Registry Numbers
MDL Number MFCD08275692
inventory_2 Storage & Handling
Storage 2-8°C, avoiding light

description Product Description

Used in organic synthesis as a protected amino acid derivative, particularly in the preparation of biologically active compounds. Its Boc-protected amine group allows for controlled deprotection in peptide-like sequences, making it valuable in medicinal chemistry for building heterocyclic scaffolds. Commonly employed in the development of pharmaceuticals and agrochemicals where the thiophene ring acts as a stable aromatic core. Also utilized in materials science for constructing conjugated systems in organic semiconductors due to the electron-rich nature of the thiophene moiety.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿5,040.00
Methyl4-((tert-butoxycarbonyl)amino)thiophene-3-carboxylate
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Used in organic synthesis as a protected amino acid derivative, particularly in the preparation of biologically active compounds. Its Boc-protected amine group allows for controlled deprotection in peptide-like sequences, making it valuable in medicinal chemistry for building heterocyclic scaffolds. Commonly employed in the development of pharmaceuticals and agrochemicals where the thiophene ring acts as a stable aromatic core. Also utilized in materials science for constructing conjugated systems in org

Used in organic synthesis as a protected amino acid derivative, particularly in the preparation of biologically active compounds. Its Boc-protected amine group allows for controlled deprotection in peptide-like sequences, making it valuable in medicinal chemistry for building heterocyclic scaffolds. Commonly employed in the development of pharmaceuticals and agrochemicals where the thiophene ring acts as a stable aromatic core. Also utilized in materials science for constructing conjugated systems in organic semiconductors due to the electron-rich nature of the thiophene moiety.

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