N-(3-Aminophenyl)propionamide

98%

Reagent Code: #219465
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CAS Number 22987-10-6

science Other reagents with same CAS 22987-10-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 164.20 g/mol
Formula C₉H₁₂N₂O
badge Registry Numbers
MDL Number MFCD00044021
inventory_2 Storage & Handling
Storage Room temperature, seal, dry, light-proof

description Product Description

Used as an intermediate in the synthesis of dyes and pharmaceuticals. It plays a role in the development of certain azo dyes due to the presence of the aromatic amine group, which can undergo diazotization and coupling reactions. Also explored in medicinal chemistry for the design of bioactive molecules, particularly in the development of anti-inflammatory and antimicrobial agents. Its amide and amine functionalities make it suitable for use in peptide-like structures and heterocyclic compound synthesis.

Available Sizes & Pricing

Size Availability Unit Price Quantity
5g
10-20 days ฿1,360.00
25g
10-20 days ฿5,300.00
100g
10-20 days ฿19,860.00
N-(3-Aminophenyl)propionamide
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Used as an intermediate in the synthesis of dyes and pharmaceuticals. It plays a role in the development of certain azo dyes due to the presence of the aromatic amine group, which can undergo diazotization and coupling reactions. Also explored in medicinal chemistry for the design of bioactive molecules, particularly in the development of anti-inflammatory and antimicrobial agents. Its amide and amine functionalities make it suitable for use in peptide-like structures and heterocyclic compound synthesis.

Used as an intermediate in the synthesis of dyes and pharmaceuticals. It plays a role in the development of certain azo dyes due to the presence of the aromatic amine group, which can undergo diazotization and coupling reactions. Also explored in medicinal chemistry for the design of bioactive molecules, particularly in the development of anti-inflammatory and antimicrobial agents. Its amide and amine functionalities make it suitable for use in peptide-like structures and heterocyclic compound synthesis.

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