2-amino-N-methoxy-N-methylbenzamide

95%

Reagent Code: #219152
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CAS Number 133776-41-7

science Other reagents with same CAS 133776-41-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 180.20 g/mol
Formula C₉H₁₂N₂O₂
badge Registry Numbers
MDL Number MFCD12095390
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of bioactive molecules and pharmaceuticals. It serves as a building block in the formation of benzoxazole and benzimidazole derivatives, which are common scaffolds in drug discovery. Its structure allows for efficient cyclization reactions, making it valuable in the development of kinase inhibitors and antimicrobial agents. Also utilized in peptide coupling strategies due to the presence of both amine and amide functionalities, enabling selective modifications in complex molecule assembly.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿9,490.00
inventory 250mg
10-20 days ฿17,820.00
inventory 1g
10-20 days ฿35,610.00

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2-amino-N-methoxy-N-methylbenzamide
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Used as an intermediate in organic synthesis, particularly in the preparation of bioactive molecules and pharmaceuticals. It serves as a building block in the formation of benzoxazole and benzimidazole derivatives, which are common scaffolds in drug discovery. Its structure allows for efficient cyclization reactions, making it valuable in the development of kinase inhibitors and antimicrobial agents. Also utilized in peptide coupling strategies due to the presence of both amine and amide functionalities,

Used as an intermediate in organic synthesis, particularly in the preparation of bioactive molecules and pharmaceuticals. It serves as a building block in the formation of benzoxazole and benzimidazole derivatives, which are common scaffolds in drug discovery. Its structure allows for efficient cyclization reactions, making it valuable in the development of kinase inhibitors and antimicrobial agents. Also utilized in peptide coupling strategies due to the presence of both amine and amide functionalities, enabling selective modifications in complex molecule assembly.

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