Tert-Butyl 2-Amino-1-(Methoxymethyl)Ethylcarbamate

95%

Reagent Code: #242918
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CAS Number 140887-54-3

science Other reagents with same CAS 140887-54-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 204.27 g/mol
Formula C₉H₂₀N₂O₃
badge Registry Numbers
MDL Number MFCD20441496
thermostat Physical Properties
Boiling Point 315.6±32.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.022±0.06 g/cm3(Predicted)
Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of beta-amino alcohols and chiral building blocks for drug development. Commonly employed in the preparation of protease inhibitors and other biologically active molecules due to its ability to act as a protected amino alcohol derivative. Its tert-butyloxycarbonyl (Boc) group allows for selective deprotection under mild acidic conditions, making it valuable in multi-step organic syntheses, especially in peptide and peptidomimetic chemistry.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿36,410.00
inventory 250mg
10-20 days ฿67,070.00

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Tert-Butyl 2-Amino-1-(Methoxymethyl)Ethylcarbamate
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of beta-amino alcohols and chiral building blocks for drug development. Commonly employed in the preparation of protease inhibitors and other biologically active molecules due to its ability to act as a protected amino alcohol derivative. Its tert-butyloxycarbonyl (Boc) group allows for selective deprotection under mild acidic conditions, making it valuable in multi-step organic syntheses, especially in peptide an

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of beta-amino alcohols and chiral building blocks for drug development. Commonly employed in the preparation of protease inhibitors and other biologically active molecules due to its ability to act as a protected amino alcohol derivative. Its tert-butyloxycarbonyl (Boc) group allows for selective deprotection under mild acidic conditions, making it valuable in multi-step organic syntheses, especially in peptide and peptidomimetic chemistry.

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