N-methoxy-N-methylcyclobutanecarboxamide

97%

Reagent Code: #218063
label
Alias N-methoxy-N-methylcyclobutanecarboxamide
fingerprint
CAS Number 640768-72-5

science Other reagents with same CAS 640768-72-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 143.18362 g/mol
Formula C₇H₁₃NO₂
badge Registry Numbers
MDL Number MFCD12546237
thermostat Physical Properties
Boiling Point 176.8±23.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.081±0.06 g/cm3(Predicted)
Storage Room temperature

description Product Description

N-Methoxy-N-methylcyclobutanecarboxamide is a Weinreb amide used in organic synthesis for the selective formation of ketones. It reacts with organometallic reagents, such as Grignard or organolithium compounds, to generate stable chelated intermediates that prevent over-addition, yielding ketones upon hydrolysis. This reagent is particularly useful in the synthesis of complex organic molecules, including pharmaceuticals and natural products, where precise control over carbonyl functionality is essential. The cyclobutane moiety may impart specific steric or reactivity profiles for targeted applications in medicinal chemistry.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿740.00
inventory 5g
10-20 days ฿3,520.00
N-methoxy-N-methylcyclobutanecarboxamide
No image available

N-Methoxy-N-methylcyclobutanecarboxamide is a Weinreb amide used in organic synthesis for the selective formation of ketones. It reacts with organometallic reagents, such as Grignard or organolithium compounds, to generate stable chelated intermediates that prevent over-addition, yielding ketones upon hydrolysis. This reagent is particularly useful in the synthesis of complex organic molecules, including pharmaceuticals and natural products, where precise control over carbonyl functionality is essential.

N-Methoxy-N-methylcyclobutanecarboxamide is a Weinreb amide used in organic synthesis for the selective formation of ketones. It reacts with organometallic reagents, such as Grignard or organolithium compounds, to generate stable chelated intermediates that prevent over-addition, yielding ketones upon hydrolysis. This reagent is particularly useful in the synthesis of complex organic molecules, including pharmaceuticals and natural products, where precise control over carbonyl functionality is essential. The cyclobutane moiety may impart specific steric or reactivity profiles for targeted applications in medicinal chemistry.

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...