2-Amino-3-methoxybenzamide

98%

Reagent Code: #139007
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CAS Number 106782-78-9

science Other reagents with same CAS 106782-78-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 166.18 g/mol
Formula C₈H₁₀N₂O₂
badge Registry Numbers
MDL Number MFCD09753573
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry, light-proof

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and anti-cancer agents. Its structure allows for easy functionalization, making it valuable in medicinal chemistry for building complex heterocyclic compounds. Commonly employed in the preparation of benzoxazole and quinazoline derivatives, which exhibit biological activity such as anti-inflammatory and antimicrobial effects. Also utilized in research settings for designing enzyme inhibitors due to its ability to interact with active sites through hydrogen bonding and aromatic interactions.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,210.00
inventory 250mg
10-20 days ฿5,450.00
inventory 1g
10-20 days ฿14,710.00

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2-Amino-3-methoxybenzamide
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and anti-cancer agents. Its structure allows for easy functionalization, making it valuable in medicinal chemistry for building complex heterocyclic compounds. Commonly employed in the preparation of benzoxazole and quinazoline derivatives, which exhibit biological activity such as anti-inflammatory and antimicrobial effects. Also utilized in research settings for designing enzyme inhibito

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and anti-cancer agents. Its structure allows for easy functionalization, making it valuable in medicinal chemistry for building complex heterocyclic compounds. Commonly employed in the preparation of benzoxazole and quinazoline derivatives, which exhibit biological activity such as anti-inflammatory and antimicrobial effects. Also utilized in research settings for designing enzyme inhibitors due to its ability to interact with active sites through hydrogen bonding and aromatic interactions.

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