N-Ethyl-N-methylcarbamoyl Chloride

98%

Reagent Code: #121462
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CAS Number 42252-34-6

science Other reagents with same CAS 42252-34-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 121.57 g/mol
Formula C₄H₈ClNO
badge Registry Numbers
MDL Number MFCD08061404
inventory_2 Storage & Handling
Storage 2~8℃

description Product Description

Used primarily in organic synthesis, it serves as a key intermediate in the production of various pharmaceuticals and agrochemicals. It is particularly valuable in the synthesis of carbamate compounds, which are widely used as insecticides, herbicides, and fungicides. Additionally, it plays a role in the development of certain drugs, including those targeting neurological disorders, by facilitating the introduction of carbamoyl groups into molecular structures. Its reactivity with amines and alcohols makes it a versatile reagent in constructing complex organic molecules.

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Test Parameter Specification
Purity (%) 98-100%

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Size Availability Unit Price Quantity
inventory 100g
10-20 days ฿7,360.00
inventory 500g
10-20 days ฿36,050.00
inventory 25g
10-20 days ฿2,000.00
inventory 5g
10-20 days ฿580.00

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N-Ethyl-N-methylcarbamoyl Chloride
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Used primarily in organic synthesis, it serves as a key intermediate in the production of various pharmaceuticals and agrochemicals. It is particularly valuable in the synthesis of carbamate compounds, which are widely used as insecticides, herbicides, and fungicides. Additionally, it plays a role in the development of certain drugs, including those targeting neurological disorders, by facilitating the introduction of carbamoyl groups into molecular structures. Its reactivity with amines and alcohols mak

Used primarily in organic synthesis, it serves as a key intermediate in the production of various pharmaceuticals and agrochemicals. It is particularly valuable in the synthesis of carbamate compounds, which are widely used as insecticides, herbicides, and fungicides. Additionally, it plays a role in the development of certain drugs, including those targeting neurological disorders, by facilitating the introduction of carbamoyl groups into molecular structures. Its reactivity with amines and alcohols makes it a versatile reagent in constructing complex organic molecules.

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