Atomfair Dimethylformamide diethylacetal C7H17NO2

Description Dimethylformamide Diethylacetal (CAS No. 1188-33-6) is a highly versatile and reactive organonitrogen compound with the molecular formula C7H17NO2. Also known as 1,1-Diethoxy-N,N-dimethylmethanamine , this clear to pale yellow liquid is widely utilized as a key reagent in organic synthesis, particularly in the formation of enamines, Vilsmeier-Haack reactions, and as a protecting group for aldehydes. Its unique structure, featuring both diethoxy and dimethylamino functional groups, makes it an excellent electrophile and a valuable intermediate in pharmaceutical and agrochemical manufacturing. With a purity of ??98%, our product is rigorously tested to meet the highest industry standards, ensuring consistent performance in sensitive…

Description

Dimethylformamide Diethylacetal (CAS No. 1188-33-6) is a highly versatile and reactive organonitrogen compound with the molecular formula C₇H₁₇NO₂. Also known as 1,1-Diethoxy-N,N-dimethylmethanamine, this clear to pale yellow liquid is widely utilized as a key reagent in organic synthesis, particularly in the formation of enamines, Vilsmeier-Haack reactions, and as a protecting group for aldehydes. Its unique structure, featuring both diethoxy and dimethylamino functional groups, makes it an excellent electrophile and a valuable intermediate in pharmaceutical and agrochemical manufacturing. With a purity of ??98%, our product is rigorously tested to meet the highest industry standards, ensuring consistent performance in sensitive applications. Store under inert conditions to maintain stability.

CAS No: 1188-33-6
Molecular Formula: C7H17NO2
Molecular Weight: 147.22
Exact Mass: 147.125928785
Monoisotopic Mass: 147.125928785
IUPAC Name: 1,1-diethoxy-N,N-dimethylmethanamine
SMILES: CCOC(N(C)C)OCC
Synonyms: 1188-33-6, 1,1-Diethoxy-N,N-dimethylmethanamine, N,N-Dimethylformamide diethyl acetal, 1,1-Diethoxytrimethylamine, Methanamine, 1,1-diethoxy-N,N-dimethyl-

Application

Dimethylformamide Diethylacetal is primarily employed as a reagent in organic synthesis for the preparation of enamines and as a precursor in Vilsmeier-Haack reactions to form aromatic aldehydes. It serves as a protecting group for aldehydes in multistep synthetic routes, particularly in pharmaceutical intermediates. Additionally, it finds use in the synthesis of heterocyclic compounds and as a catalyst or co-reactant in specialized polymerization processes.

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