N-Methoxy-N-methyl-2,2,2-trifluoroacetamide

98%

Reagent Code: #56430
label
Alias N-methoxy-N-methyltrifluoroacetamide
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CAS Number 104863-67-4

science Other reagents with same CAS 104863-67-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 157.09 g/mol
Formula C₄H₆F₃NO₂
badge Registry Numbers
MDL Number MFCD00077565
thermostat Physical Properties
Boiling Point 53 °C30 mm Hg(lit.)
inventory_2 Storage & Handling
Density 1.299 g/mL at 25 °C(lit.)
Storage room temperature

description Product Description

This chemical is primarily utilized as a versatile reagent in organic synthesis, particularly in the preparation of trifluoromethylated compounds. It serves as a trifluoroacetylating agent, enabling the introduction of the trifluoroacetyl group into various substrates, which is valuable in the development of pharmaceuticals and agrochemicals. Additionally, it is employed in the synthesis of peptides and other bioactive molecules, where its ability to act as a protecting group for amines is highly advantageous. Its stability and reactivity make it a useful tool in constructing complex molecular structures, especially in medicinal chemistry research.

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Test Parameter Specification
Purity (GC) 98-100%
Appearance colorless liquid
Infrared Spectrum Conforms to Structure
Proton NMR Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5ml
10-20 days ฿880.00
inventory 25ml
10-20 days ฿3,360.00
inventory 100ml
10-20 days ฿11,990.00

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N-Methoxy-N-methyl-2,2,2-trifluoroacetamide
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This chemical is primarily utilized as a versatile reagent in organic synthesis, particularly in the preparation of trifluoromethylated compounds. It serves as a trifluoroacetylating agent, enabling the introduction of the trifluoroacetyl group into various substrates, which is valuable in the development of pharmaceuticals and agrochemicals. Additionally, it is employed in the synthesis of peptides and other bioactive molecules, where its ability to act as a protecting group for amines is highly advanta

This chemical is primarily utilized as a versatile reagent in organic synthesis, particularly in the preparation of trifluoromethylated compounds. It serves as a trifluoroacetylating agent, enabling the introduction of the trifluoroacetyl group into various substrates, which is valuable in the development of pharmaceuticals and agrochemicals. Additionally, it is employed in the synthesis of peptides and other bioactive molecules, where its ability to act as a protecting group for amines is highly advantageous. Its stability and reactivity make it a useful tool in constructing complex molecular structures, especially in medicinal chemistry research.

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