N-Methoxy-N-methylpentanamide

97%

Reagent Code: #52667
fingerprint
CAS Number 129118-11-2

science Other reagents with same CAS 129118-11-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 145.2 g/mol
Formula C₇H₁₅NO₂
badge Registry Numbers
MDL Number MFCD05149014
inventory_2 Storage & Handling
Storage room temperature

description Product Description

N-Methoxy-N-methylpentanamide is a Weinreb amide derivative widely utilized in organic synthesis, particularly for the selective preparation of ketones. It functions as a key intermediate derived from pentanoic acid, enabling controlled addition of organometallic reagents (such as Grignard or organolithium compounds) to form methyl ketones without over-addition to tertiary alcohols. This chelation-stabilized reactivity makes it essential in the synthesis of pharmaceuticals, agrochemicals, and other complex organic molecules. It is especially valuable in multi-step processes for developing active pharmaceutical ingredients (APIs) and specialty chemicals, offering high efficiency, selectivity, and stability under various reaction conditions.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,359.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
N-Methoxy-N-methylpentanamide
No image available

N-Methoxy-N-methylpentanamide is a Weinreb amide derivative widely utilized in organic synthesis, particularly for the selective preparation of ketones. It functions as a key intermediate derived from pentanoic acid, enabling controlled addition of organometallic reagents (such as Grignard or organolithium compounds) to form methyl ketones without over-addition to tertiary alcohols. This chelation-stabilized reactivity makes it essential in the synthesis of pharmaceuticals, agrochemicals, and other compl

N-Methoxy-N-methylpentanamide is a Weinreb amide derivative widely utilized in organic synthesis, particularly for the selective preparation of ketones. It functions as a key intermediate derived from pentanoic acid, enabling controlled addition of organometallic reagents (such as Grignard or organolithium compounds) to form methyl ketones without over-addition to tertiary alcohols. This chelation-stabilized reactivity makes it essential in the synthesis of pharmaceuticals, agrochemicals, and other complex organic molecules. It is especially valuable in multi-step processes for developing active pharmaceutical ingredients (APIs) and specialty chemicals, offering high efficiency, selectivity, 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...