Page last updated: 2024-11-05

diazoacetic ester

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

Description

Diazoacetic ester is a yellow, oily liquid with the formula N2CHCO2R, where R is an alkyl group. It is a highly reactive compound that is used in organic synthesis as a source of carbenes. It can be synthesized by the reaction of ethyl chloroacetate with hydrazine. Diazoacetic ester is a versatile reagent that has been used in a wide range of organic reactions, including the synthesis of cyclopropanes, aziridines, and pyrroles. It has also been used in the development of new pharmaceuticals and pesticides. The compound is particularly important in organic chemistry due to its ability to participate in a variety of reactions, often serving as a source of carbenes. Carbenes are highly reactive species with a divalent carbon atom, which makes them useful in various organic transformations, such as the synthesis of new molecules and the study of reaction mechanisms. Diazoacetic ester is a valuable reagent for researchers studying organic chemistry because of its ability to form carbenes and its versatility in various organic reactions. Its potential applications in areas like pharmaceuticals and pesticides further highlight its importance.'

diazoacetic ester: structure [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID12192
CHEMBL ID4212182
SCHEMBL ID4412
MeSH IDM0100394

Synonyms (49)

Synonym
diazoacetic ester
diazoacetic acid ethyl ester
ethoxycarbonyldiazomethane
nsc79147
nsc-79147
unii-n84b835fmr
n84b835fmr ,
diazoessigsaeure-aethylester
LS-12985
ethyl 2-diazoacetate
acetic acid, diazo-, ethyl ester
ethyl diazoacetate ,
einecs 210-810-8
ccris 1403
ethyldiazoacetate
diazoacetic acid, ethyl ester
daae
nsc 79147
ai3-52121
diazoessigsaeure-aethylester [german]
623-73-4
ethyl diazoacetate, contains >=13 wt. % dichloromethane
ethyl-2-diazoacetate
(e)-2-diazonio-1-ethoxyethenolate
(e)-2-diazonio-1-ethoxy-ethenolate
A833745
AKOS005259800
ethyl diazo acetate
SCHEMBL4412
diazoacetic ester [mi]
diazo-acetic acid ethyl ester
ethyl diazoethanoate
ethylenediaminedihydrochloride
ethyl2-diazoacetate
F0001-1674
ethyl diazoacetate, purum
BBL102482
ethyldiazoacetate, contains 15 wt. % dichloromethane
STL556285
BCP21655
Q3026455
YVPJCJLMRRTDMQ-ONEGZZNKSA-N
D87242
DTXSID10878732
ethyl diazoacetate contains =13 wt. % dichloromethane
CHEMBL4212182
AKOS037517259
492994-20-4
EN300-36592
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (43)

TimeframeStudies, This Drug (%)All Drugs %
pre-19906 (13.95)18.7374
1990's1 (2.33)18.2507
2000's20 (46.51)29.6817
2010's14 (32.56)24.3611
2020's2 (4.65)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 31.71

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 Index31.71 (24.57)
Research Supply Index3.78 (2.92)
Research Growth Index6.01 (4.65)
Search Engine Demand Index30.68 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (31.71)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews2 (4.65%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other41 (95.35%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]