tert-Butyl methyl(2-oxopropyl)carbamate

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Reagent Code: #131159
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CAS Number 532410-39-2

science Other reagents with same CAS 532410-39-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 187.24 g/mol
Formula C₉H₁₇NO₃
badge Registry Numbers
MDL Number MFCD24475626
thermostat Physical Properties
Boiling Point 241.9±19.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.012±0.06 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

Used as an intermediate in organic synthesis, particularly in the pharmaceutical industry for constructing complex molecules. Its structure allows for selective protection of amine groups, making it valuable in multi-step synthesis where controlled reactivity is needed. The carbamate group stabilizes the amine while enabling deprotection under mild conditions, which is useful in peptide and heterocycle synthesis. Additionally, the ketone functionality provides a site for further chemical modifications, such as reductions or condensation reactions, enabling the development of active pharmaceutical ingredients (APIs) and functionalized amines.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿21,650.00
inventory 5g
10-20 days ฿75,750.00

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tert-Butyl methyl(2-oxopropyl)carbamate
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Used as an intermediate in organic synthesis, particularly in the pharmaceutical industry for constructing complex molecules. Its structure allows for selective protection of amine groups, making it valuable in multi-step synthesis where controlled reactivity is needed. The carbamate group stabilizes the amine while enabling deprotection under mild conditions, which is useful in peptide and heterocycle synthesis. Additionally, the ketone functionality provides a site for further chemical modifications, s

Used as an intermediate in organic synthesis, particularly in the pharmaceutical industry for constructing complex molecules. Its structure allows for selective protection of amine groups, making it valuable in multi-step synthesis where controlled reactivity is needed. The carbamate group stabilizes the amine while enabling deprotection under mild conditions, which is useful in peptide and heterocycle synthesis. Additionally, the ketone functionality provides a site for further chemical modifications, such as reductions or condensation reactions, enabling the development of active pharmaceutical ingredients (APIs) and functionalized amines.

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