Page last updated: 2024-12-06

ethyl acetimidate

Description Research Excerpts Clinical Trials Roles Classes Pathways Study Profile Bioassays Related Drugs Related Conditions Protein Interactions Research Growth Market Indicators

Description

Ethyl acetimidate is a chemical compound with the formula CH3C(NH)OCH2CH3. It is a colorless liquid with a pungent odor. Ethyl acetimidate is a versatile reagent used in organic synthesis, particularly in the formation of amides and amidines. It is also a key intermediate in the production of various pharmaceuticals and agrochemicals. The synthesis of ethyl acetimidate typically involves the reaction of ethyl acetate with ammonia in the presence of a catalyst. Its reactivity stems from the electrophilic carbon atom in the imidate functional group, allowing it to participate in a range of nucleophilic substitution reactions. Ethyl acetimidate is studied extensively due to its diverse applications in organic synthesis and its potential use as a building block for the synthesis of various bioactive molecules. Its properties, particularly its reactivity and stability, make it a valuable tool for researchers exploring new synthetic routes and developing novel pharmaceuticals.'

ethyl acetimidate: RN given refers to parent cpd [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID65066
MeSH IDM0063105

Synonyms (19)

Synonym
1-ethoxy-ethylidene-amine
ethanimidic acid, ethyl ester
ethyl acetimidate
ethyl ethanimidate
STL257101
ethyl ethanimidoate
AKOS005174594
1000-84-6
einecs 213-676-9
1-ethoxyethanimine
ethyl acetoimidate
ethyl ethaneimidate
o-ethyl acetimidate
DTXSID4061381
ehtyl acetimidate
ethyl ethanimidoate #
FT-0764042
athylacetiminoa currencyther
A926739

Research Excerpts

Treatment

ExcerptReferenceRelevance
"Treatment with ethyl acetimidate caused an irreversible reduction of Na currents and a shift of the voltage dependence of the steady-state sodium inactivation, h infinity (E), in the hyperpolarizing direction."( Effects of chemical modification of amino groups by two different imidoesters on voltage-clamped nerve fibres of the frog.
Rack, M, 1985
)
0.61
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (24)

TimeframeStudies, This Drug (%)All Drugs %
pre-199019 (79.17)18.7374
1990's5 (20.83)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 31.05

According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be moderate demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index31.05 (24.57)
Research Supply Index3.22 (2.92)
Research Growth Index4.31 (4.65)
Search Engine Demand Index36.91 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (31.05)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews0 (0.00%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other24 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]