tert-Butyl (3-formylphenyl)carbamate

95%

Reagent Code: #145236
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CAS Number 176980-36-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 221.25 g/mol
Formula C₁₂H₁₅NO₃
badge Registry Numbers
MDL Number MFCD06660380
thermostat Physical Properties
Melting Point 88°C
Boiling Point 290.6°C
inventory_2 Storage & Handling
Storage 2-8°C, inert gas atmosphere

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and fine chemicals, particularly in the development of active pharmaceutical ingredients (APIs) where aldehyde functionality allows for further derivatization, such as reductive amination or condensation reactions. Its protected amine group enables selective reaction at the aldehyde site, making it valuable in multi-step organic syntheses. Commonly employed in the preparation of drug candidates targeting central nervous system disorders and inflammatory diseases due to its structural compatibility with bioactive molecules. Also utilized in the creation of building blocks for combinatorial chemistry and library synthesis in drug discovery.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿500.00
inventory 1g
10-20 days ฿1,350.00
inventory 5g
10-20 days ฿6,540.00
inventory 25g
10-20 days ฿18,900.00
tert-Butyl (3-formylphenyl)carbamate
Used as an intermediate in the synthesis of pharmaceuticals and fine chemicals, particularly in the development of active pharmaceutical ingredients (APIs) where aldehyde functionality allows for further derivatization, such as reductive amination or condensation reactions. Its protected amine group enables selective reaction at the aldehyde site, making it valuable in multi-step organic syntheses. Commonly employed in the preparation of drug candidates targeting central nervous system disorders and inflammatory diseases due to its structural compatibility with bioactive molecules. Also utilized in the creation of building blocks for combinatorial chemistry and library synthesis in drug discovery.
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