tert-Butyl(2-(methylamino)-2-oxoethyl)carbamate

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Reagent Code: #82836
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CAS Number 88815-85-4

science Other reagents with same CAS 88815-85-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 188.22 g/mol
Formula C₈H₁₆N₂O₃
badge Registry Numbers
MDL Number MFCD21104090
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This compound, tert-Butyl(2-(methylamino)-2-oxoethyl)carbamate, is a Boc-protected amino acid derivative used as an intermediate in organic synthesis. It features a tert-butoxycarbonyl (Boc) protecting group on the amine, which provides stability under various conditions and enables selective deprotection. This makes it particularly useful in peptide chemistry and the preparation of pharmaceutical intermediates, where it helps maintain the integrity of sensitive functional groups during the assembly of complex molecules. Its applications also extend to the development of bioactive compounds requiring precise control over reaction selectivity.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿4,500.00
inventory 1g
10-20 days ฿9,261.00
inventory 5g
10-20 days ฿24,750.00

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tert-Butyl(2-(methylamino)-2-oxoethyl)carbamate
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This compound, tert-Butyl(2-(methylamino)-2-oxoethyl)carbamate, is a Boc-protected amino acid derivative used as an intermediate in organic synthesis. It features a tert-butoxycarbonyl (Boc) protecting group on the amine, which provides stability under various conditions and enables selective deprotection. This makes it particularly useful in peptide chemistry and the preparation of pharmaceutical intermediates, where it helps maintain the integrity of sensitive functional groups during the assembly of c

This compound, tert-Butyl(2-(methylamino)-2-oxoethyl)carbamate, is a Boc-protected amino acid derivative used as an intermediate in organic synthesis. It features a tert-butoxycarbonyl (Boc) protecting group on the amine, which provides stability under various conditions and enables selective deprotection. This makes it particularly useful in peptide chemistry and the preparation of pharmaceutical intermediates, where it helps maintain the integrity of sensitive functional groups during the assembly of complex molecules. Its applications also extend to the development of bioactive compounds requiring precise control over reaction selectivity.

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