N-Methoxy-N-methylcarbamoyl Chloride

≥98%(GC)(T)

Reagent Code: #217608
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CAS Number 30289-28-2

science Other reagents with same CAS 30289-28-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 123.54 g/mol
Formula C₃H₆ClNO₂
badge Registry Numbers
MDL Number MFCD06658962
thermostat Physical Properties
Boiling Point 60°C|18mmHg(lit.)
inventory_2 Storage & Handling
Density 1.22
Storage Room temperature, dryness, inert gas storage

description Product Description

Used primarily as an intermediate in organic synthesis, this compound is valuable in the preparation of urea and carbamate derivatives, which are important in the development of pharmaceuticals and agrochemicals. It serves as a reagent for introducing the N-methoxy-N-methylcarbamoyl group under mild conditions, making it useful in peptide synthesis and the construction of complex molecules where functional group compatibility is crucial. Its reactivity allows for efficient coupling reactions with amines to form urea products and with alcohols to form carbamate products, often used in multi-step synthetic routes. Due to its moisture sensitivity, it is typically handled under anhydrous conditions in controlled environments.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿2,540.00
1g
10-20 days ฿5,460.00
N-Methoxy-N-methylcarbamoyl Chloride
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Used primarily as an intermediate in organic synthesis, this compound is valuable in the preparation of urea and carbamate derivatives, which are important in the development of pharmaceuticals and agrochemicals. It serves as a reagent for introducing the N-methoxy-N-methylcarbamoyl group under mild conditions, making it useful in peptide synthesis and the construction of complex molecules where functional group compatibility is crucial. Its reactivity allows for efficient coupling reactions with amines to
Used primarily as an intermediate in organic synthesis, this compound is valuable in the preparation of urea and carbamate derivatives, which are important in the development of pharmaceuticals and agrochemicals. It serves as a reagent for introducing the N-methoxy-N-methylcarbamoyl group under mild conditions, making it useful in peptide synthesis and the construction of complex molecules where functional group compatibility is crucial. Its reactivity allows for efficient coupling reactions with amines to form urea products and with alcohols to form carbamate products, often used in multi-step synthetic routes. Due to its moisture sensitivity, it is typically handled under anhydrous conditions in controlled environments.
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