N-Methoxy-N-methylchroman-2-carboxamide

95%

Reagent Code: #219319
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CAS Number 2007908-54-3

science Other reagents with same CAS 2007908-54-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 221.25 g/mol
Formula C₁₂H₁₅NO₃
badge Registry Numbers
MDL Number MFCD30472055
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

N-Methoxy-N-methylchroman-2-carboxamide is a specific Weinreb amide derived from chroman-2-carboxylic acid, used as a reagent in organic synthesis. It enables the controlled conversion into ketones or aldehydes by reacting with organometallic reagents such as Grignard or organolithium compounds. Its stability and selectivity make it valuable in multi-step synthesis of complex molecules, including natural products and pharmaceuticals. Commonly employed when precise carbonyl chain elongation is required without over-addition of nucleophiles.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,410.00
inventory 250mg
10-20 days ฿10,690.00
inventory 1g
10-20 days ฿21,380.00
N-Methoxy-N-methylchroman-2-carboxamide
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N-Methoxy-N-methylchroman-2-carboxamide is a specific Weinreb amide derived from chroman-2-carboxylic acid, used as a reagent in organic synthesis. It enables the controlled conversion into ketones or aldehydes by reacting with organometallic reagents such as Grignard or organolithium compounds. Its stability and selectivity make it valuable in multi-step synthesis of complex molecules, including natural products and pharmaceuticals. Commonly employed when precise carbonyl chain elongation is required wi

N-Methoxy-N-methylchroman-2-carboxamide is a specific Weinreb amide derived from chroman-2-carboxylic acid, used as a reagent in organic synthesis. It enables the controlled conversion into ketones or aldehydes by reacting with organometallic reagents such as Grignard or organolithium compounds. Its stability and selectivity make it valuable in multi-step synthesis of complex molecules, including natural products and pharmaceuticals. Commonly employed when precise carbonyl chain elongation is required without over-addition of nucleophiles.

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