Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references
Chemical compound
Succinaldehyde or succindialdehyde is an organic compound with the formula (C2H4(CHO)2. It is a colorless viscous liquid.[2] Typical of some other saturated dialdehydes, succinaldehyde is handled as the hydrates or methanol-derived acetal. It is a precursor to tropinone.[3] Succinaldehyde can be used as a crosslinking agent for proteins, but it is less widely used than the related dialdehyde glutaraldehyde.
^International Union of Pure and Applied Chemistry (2014). Nomenclature of Organic Chemistry: IUPAC Recommendations and Preferred Names 2013. The Royal Society of Chemistry. p. 908. doi:10.1039/9781849733069. ISBN 978-0-85404-182-4.
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Succinaldehyde or succindialdehyde is an organic compound with the formula (C2H4(CHO)2. It is a colorless viscous liquid. Typical of some other saturated...
ethyl acetoacetate (although it is prepared by ethanolysis of ketene). Succinaldehyde (CH2CHO)2 is the simplest and parent 1,4-dialdehyde. The aromatic derivative...
molecule, but the reactants used in its preparation are fairly simple: succinaldehyde, methylamine and acetonedicarboxylic acid (or even acetone). The synthesis...
Nicholls, A. C.; Rydon, H. N. (1972). "The Hydration and Polymerisation of Succinaldehyde, Glutaraldehyde, and Adipaldehyde". Journal of the Chemical Society...
they can be derived. An example is butanedial, which is also called succinaldehyde (from succinic acid). Some aldehydes are substrates for aldehyde dehydrogenase...
classical Robinson tropinone synthesis, using glutaraldehyde (rather than succinaldehyde), acetonedicarboxylic acid, and methylammonium chloride. It was the...
2-[2-(5,5,8a-trimethyl-2-methylene-decahydro-naphthalen-1-yl)-ethylidene]-succinaldehyde against Ophiophagus hannah venom". The Journal of Pharmacy and Pharmacology...
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