4-Amino-N-methylbenzamide

98%

Reagent Code: #135256
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CAS Number 6274-22-2

science Other reagents with same CAS 6274-22-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 150.18 g/mol
Formula C₈H₁₀N₂O
badge Registry Numbers
MDL Number MFCD00665792
inventory_2 Storage & Handling
Storage Room temperature, sealed

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other bioactive molecules. It serves as a building block in medicinal chemistry due to the presence of both amine and amide functional groups, enabling conjugation and derivatization for drug design. Also employed in the preparation of fluorescent probes and labeled compounds for biochemical assays. Its structural properties make it suitable for research in organic synthesis and structure-activity relationship studies.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿300.00
inventory 5g
10-20 days ฿380.00
inventory 25g
10-20 days ฿660.00
inventory 100g
10-20 days ฿1,510.00
inventory 500g
10-20 days ฿7,520.00
4-Amino-N-methylbenzamide
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other bioactive molecules. It serves as a building block in medicinal chemistry due to the presence of both amine and amide functional groups, enabling conjugation and derivatization for drug design. Also employed in the preparation of fluorescent probes and labeled compounds for biochemical assays. Its structural properties make it suitable for research in organic synthesis and structure

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other bioactive molecules. It serves as a building block in medicinal chemistry due to the presence of both amine and amide functional groups, enabling conjugation and derivatization for drug design. Also employed in the preparation of fluorescent probes and labeled compounds for biochemical assays. Its structural properties make it suitable for research in organic synthesis and structure-activity relationship studies.

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