Page last updated: 2024-11-05

succindialdehyde

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

Succindialdehyde, also known as butanedial, is a four-carbon dialdehyde that serves as a valuable building block in organic synthesis. It is a colorless liquid with a pungent odor. Succindialdehyde can be synthesized through various methods, including the oxidation of 1,4-butanediol, the hydrolysis of 2,5-dihydrofuran, or the catalytic hydrogenation of maleic anhydride. It exhibits diverse reactivity, readily undergoing reactions such as aldol condensation, Michael addition, and Diels-Alder cycloaddition. Succindialdehyde has garnered significant interest in research due to its potential applications in the synthesis of pharmaceuticals, agrochemicals, and polymers. For instance, it is a precursor to the synthesis of various heterocyclic compounds, including pyridines, pyrroles, and furans. Furthermore, succindialdehyde has been explored as a cross-linking agent for polymers, enhancing their mechanical properties. Its biological activity has also been investigated, suggesting potential roles in the regulation of cell growth and differentiation. The study of succindialdehyde continues to advance, driven by its versatility as a synthetic building block and its potential applications in various fields.'

Cross-References

ID SourceID
PubMed CID12524
CHEBI ID80762
MeSH IDM0064833

Synonyms (30)

Synonym
beta-formylpropionaldehyde
einecs 211-333-8
unii-0503177591
nsc 11057
.beta.-formylpropionaldehyde
succinic aldehyde
butanedial
succinic dialdehyde
succinaldehyde
succindialdehyde
1,4-butanedione
638-37-9
nsc-11057
nsc11057
A834548
FT-0632716
1,4-butane dialdehyde
CHEBI:80762
antibioticji-20a
1,4-butanedial
DTXSID3021514
diacetal
BCP20105
Q4864618
E75948
succinaldehyde (40% in h2o)
FT-0724206
AMY18777
ndga derivative
EN300-85898
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (1)

ClassDescription
aldehydeA compound RC(=O)H, in which a carbonyl group is bonded to one hydrogen atom and to one R group.
[compound class information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Research

Studies (5)

TimeframeStudies, This Drug (%)All Drugs %
pre-19901 (20.00)18.7374
1990's0 (0.00)18.2507
2000's2 (40.00)29.6817
2010's2 (40.00)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: 43.08

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 strong demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index43.08 (24.57)
Research Supply Index1.79 (2.92)
Research Growth Index4.09 (4.65)
Search Engine Demand Index61.55 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (43.08)

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%
Other5 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]