tert-Butyl (5-methoxy-2-nitrophenyl)carbamate

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Reagent Code: #113357
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CAS Number 185428-55-1

science Other reagents with same CAS 185428-55-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 268.27 g/mol
Formula C₁₂H₁₆N₂O₅
badge Registry Numbers
MDL Number MFCD28043790
thermostat Physical Properties
Boiling Point 353.1±32.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed

description Product Description

Used primarily in organic synthesis, this compound serves as an intermediate in the production of more complex molecules, particularly in pharmaceutical research. It is often employed in the development of active pharmaceutical ingredients (APIs) where the tert-butyl group provides stability and the nitro group can be further reduced or modified. Additionally, its methoxy group makes it useful in constructing molecules with specific electronic properties, aiding in the study of drug-receptor interactions. Its role in peptide synthesis is also notable, as it helps protect amine groups during chemical reactions.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿6,201.00
inventory 100mg
10-20 days ฿3,105.00

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tert-Butyl (5-methoxy-2-nitrophenyl)carbamate
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Used primarily in organic synthesis, this compound serves as an intermediate in the production of more complex molecules, particularly in pharmaceutical research. It is often employed in the development of active pharmaceutical ingredients (APIs) where the tert-butyl group provides stability and the nitro group can be further reduced or modified. Additionally, its methoxy group makes it useful in constructing molecules with specific electronic properties, aiding in the study of drug-receptor interactions

Used primarily in organic synthesis, this compound serves as an intermediate in the production of more complex molecules, particularly in pharmaceutical research. It is often employed in the development of active pharmaceutical ingredients (APIs) where the tert-butyl group provides stability and the nitro group can be further reduced or modified. Additionally, its methoxy group makes it useful in constructing molecules with specific electronic properties, aiding in the study of drug-receptor interactions. Its role in peptide synthesis is also notable, as it helps protect amine groups during chemical reactions.

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