N-(4-(Benzyloxy)phenyl)-2-chloroacetamide

97%

Reagent Code: #219455
fingerprint
CAS Number 19514-92-2

science Other reagents with same CAS 19514-92-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 275.73 g/mol
Formula C₁₅H₁₄ClNO₂
badge Registry Numbers
MDL Number MFCD00791335
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as an intermediate in organic synthesis, particularly in the development of pharmaceutical compounds. It plays a role in the preparation of substituted anilides and benzyl-protected phenolic derivatives, which are common scaffolds in drug design. Its chloroacetamide group allows for further alkylation or nucleophilic substitution reactions, making it valuable in building complex molecules for medicinal chemistry research. Commonly employed in the synthesis of kinase inhibitors and anti-inflammatory agents. Also utilized in the preparation of labeled compounds for biochemical assays due to its reactivity and stability under various reaction conditions.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,180.00
inventory 1g
10-20 days ฿3,170.00
inventory 5g
10-20 days ฿11,990.00
inventory 25g
10-20 days ฿44,710.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
N-(4-(Benzyloxy)phenyl)-2-chloroacetamide
No image available

Used as an intermediate in organic synthesis, particularly in the development of pharmaceutical compounds. It plays a role in the preparation of substituted anilides and benzyl-protected phenolic derivatives, which are common scaffolds in drug design. Its chloroacetamide group allows for further alkylation or nucleophilic substitution reactions, making it valuable in building complex molecules for medicinal chemistry research. Commonly employed in the synthesis of kinase inhibitors and anti-inflammatory

Used as an intermediate in organic synthesis, particularly in the development of pharmaceutical compounds. It plays a role in the preparation of substituted anilides and benzyl-protected phenolic derivatives, which are common scaffolds in drug design. Its chloroacetamide group allows for further alkylation or nucleophilic substitution reactions, making it valuable in building complex molecules for medicinal chemistry research. Commonly employed in the synthesis of kinase inhibitors and anti-inflammatory agents. Also utilized in the preparation of labeled compounds for biochemical assays due to its reactivity and stability under various reaction conditions.

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...