N-(2,6-Dimethylphenyl)-2-hydroxyacetamide

97%

Reagent Code: #214911
fingerprint
CAS Number 29183-14-0

science Other reagents with same CAS 29183-14-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 179.22 g/mol
Formula C₁₀H₁₃NO₂
badge Registry Numbers
MDL Number MFCD08443051
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used primarily as an intermediate in the synthesis of pharmaceuticals, particularly local anesthetics such as lidocaine and related derivatives. Its structure supports the formation of amide bonds critical for bioactive molecule development. It also finds use in the preparation of agrochemicals and organic synthesis where acylated aniline derivatives are required. Due to its stability and reactivity, it serves as a building block in medicinal chemistry for designing compounds with enhanced metabolic resistance and lipophilicity.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,600.00
inventory 5g
10-20 days ฿20,680.00
inventory 1g
10-20 days ฿4,310.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
N-(2,6-Dimethylphenyl)-2-hydroxyacetamide
No image available

Used primarily as an intermediate in the synthesis of pharmaceuticals, particularly local anesthetics such as lidocaine and related derivatives. Its structure supports the formation of amide bonds critical for bioactive molecule development. It also finds use in the preparation of agrochemicals and organic synthesis where acylated aniline derivatives are required. Due to its stability and reactivity, it serves as a building block in medicinal chemistry for designing compounds with enhanced metabolic resi

Used primarily as an intermediate in the synthesis of pharmaceuticals, particularly local anesthetics such as lidocaine and related derivatives. Its structure supports the formation of amide bonds critical for bioactive molecule development. It also finds use in the preparation of agrochemicals and organic synthesis where acylated aniline derivatives are required. Due to its stability and reactivity, it serves as a building block in medicinal chemistry for designing compounds with enhanced metabolic resistance and lipophilicity.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...