N-methoxy-N-methylbenzo[d][1,3]dioxole-5-carboxamide

95%

Reagent Code: #219176
fingerprint
CAS Number 147030-72-6

science Other reagents with same CAS 147030-72-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 209.20 g/mol
Formula C₁₀H₁₁NO₄
badge Registry Numbers
MDL Number MFCD14707548
thermostat Physical Properties
Boiling Point 384.3±31.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.289±0.06 g/cm3(Predicted)
Storage Room temperature

description Product Description

Used as a key reagent in organic synthesis, particularly in the formation of Weinreb amides. It enables controlled nucleophilic addition reactions, allowing chemists to selectively produce aldehydes or ketones from carboxylic acid derivatives. This makes it valuable in the synthesis of complex natural products and pharmaceuticals where precise carbonyl group manipulation is required. Its stability and reactivity profile support high functional group tolerance, making it suitable for multi-step synthetic routes in medicinal chemistry and process development.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,360.00
inventory 250mg
10-20 days ฿11,500.00
inventory 1g
10-20 days ฿23,000.00
N-methoxy-N-methylbenzo[d][1,3]dioxole-5-carboxamide
No image available

Used as a key reagent in organic synthesis, particularly in the formation of Weinreb amides. It enables controlled nucleophilic addition reactions, allowing chemists to selectively produce aldehydes or ketones from carboxylic acid derivatives. This makes it valuable in the synthesis of complex natural products and pharmaceuticals where precise carbonyl group manipulation is required. Its stability and reactivity profile support high functional group tolerance, making it suitable for multi-step synthetic

Used as a key reagent in organic synthesis, particularly in the formation of Weinreb amides. It enables controlled nucleophilic addition reactions, allowing chemists to selectively produce aldehydes or ketones from carboxylic acid derivatives. This makes it valuable in the synthesis of complex natural products and pharmaceuticals where precise carbonyl group manipulation is required. Its stability and reactivity profile support high functional group tolerance, making it suitable for multi-step synthetic routes in medicinal chemistry and process development.

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...