N-Methoxy-N-methyl-1H-pyrrole-2-carboxamide

98%

Reagent Code: #218189
fingerprint
CAS Number 368211-06-7

science Other reagents with same CAS 368211-06-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 154.17 g/mol
Formula C₇H₁₀N₂O₂
badge Registry Numbers
MDL Number MFCD12406910
inventory_2 Storage & Handling
Storage Room temperature, dry seal

description Product Description

N-Methoxy-N-methyl-1H-pyrrole-2-carboxamide is a specialized Weinreb amide derivative utilized as a key intermediate in organic synthesis. It enables the controlled formation of ketones from the pyrrole-2-carbonyl group through reactions with organometallic reagents like Grignard or organolithium compounds, preventing over-addition and providing high selectivity. This makes it particularly useful in the preparation of bioactive molecules, pharmaceuticals, and complex natural products featuring pyrrole scaffolds. Its stability under mild conditions supports applications in sensitive substrate manipulations, including the development of enzyme inhibitors and other therapeutic agents.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿1,660.00
1g
10-20 days ฿4,480.00
N-Methoxy-N-methyl-1H-pyrrole-2-carboxamide
No image available

N-Methoxy-N-methyl-1H-pyrrole-2-carboxamide is a specialized Weinreb amide derivative utilized as a key intermediate in organic synthesis. It enables the controlled formation of ketones from the pyrrole-2-carbonyl group through reactions with organometallic reagents like Grignard or organolithium compounds, preventing over-addition and providing high selectivity. This makes it particularly useful in the preparation of bioactive molecules, pharmaceuticals, and complex natural products featuring pyrrole sc

N-Methoxy-N-methyl-1H-pyrrole-2-carboxamide is a specialized Weinreb amide derivative utilized as a key intermediate in organic synthesis. It enables the controlled formation of ketones from the pyrrole-2-carbonyl group through reactions with organometallic reagents like Grignard or organolithium compounds, preventing over-addition and providing high selectivity. This makes it particularly useful in the preparation of bioactive molecules, pharmaceuticals, and complex natural products featuring pyrrole scaffolds. Its stability under mild conditions supports applications in sensitive substrate manipulations, including the development of enzyme inhibitors and other therapeutic agents.

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...