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Chemical compound
Succinaldehyde or Butanedial is an organic compound with the formula (C2H4)(CHO)2. It is a colorless viscous liquid. Typical of some other saturated dialdehydes
Succinaldehyde
Molecule containing two adjacent C=O groups
ethyl acetoacetate (although it is prepared by ethanolysis of ketene). Succinaldehyde (CH2CHO)2 is the simplest and parent 1,4-dialdehyde. The aromatic derivative
Dicarbonyl
Index of chemical compounds with the same molecular formula
of the enol, sodium formyl acetone. Methacrylic acid Methyl acrylate Succinaldehyde Vinyl acetate This set index page lists chemical structure articles
C4H6O2
Organic compound containing the functional group R–CH=O
they can be derived. An example is butanedial, which is also called succinaldehyde (from succinic acid). Some aldehydes are substrates for aldehyde dehydrogenase
Aldehyde
Medical device
H.; Aggarwal, Varinder K. (2022). "Organocatalytic Dimerization of Succinaldehyde". Organic Syntheses. 99: 139–158. doi:10.15227/orgsyn.099.0139. Varghese
Syringe_driver
Heterocyclic organic compound,
ethers such as tetrahydrofuran. Furan slowly oxidizes in air to give succinaldehyde. Like enol ethers, 2,5-disubstituted furans are susceptible to hydrolysis
Furan
Chemical compound
molecule, but the reactants used in its preparation are fairly simple: succinaldehyde, methylamine and acetonedicarboxylic acid (or even acetone). The synthesis
Tropinone
Chemical compound
classical Robinson tropinone synthesis, using glutaraldehyde (rather than succinaldehyde), acetonedicarboxylic acid, and methylammonium chloride. It was the
Pseudopelletierine
C4H6O2 methacrylic acid 79–41–4 C4H6O2 methyl acrylate 96-33-3 C4H6O2 succinaldehyde 638-37-9 C4H6O2 vinyl acetate 108-05-4 C4H6O3 propylene carbonate 108-32-7
Glossary_of_chemical_formulae
One of four stable isomers of butanediol
1,3-Butanediol 2,3-Butanediol cis-Butene-1,4-diol Related compounds Succinaldehyde Succinic acid Except where otherwise noted, data are given for materials
1,4-Butanediol
Chemical compound
anhydride (1) by methanolysis followed by reaction with methylamine and succinaldehyde. Tropinone Findlay, Stephen P. (1957). "Concerning 2-Carbomethoxytropinone*"
2-Carbomethoxytropinone
Chemical compound
Nicholls, A. C.; Rydon, H. N. (1972). "The Hydration and Polymerisation of Succinaldehyde, Glutaraldehyde, and Adipaldehyde". Journal of the Chemical Society
Adipaldehyde
formaldehyde and 2,5-dimethoxytetrahydrofuran, which when mixed generates succinaldehyde, a noxious gas which has been likened to tear gas. Process E-6 films
E-4_process
Species of flowering plant
2-[2-(5,5,8a-trimethyl-2-methylene-decahydro-naphthalen-1-yl)-ethylidene]-succinaldehyde against Ophiophagus hannah venom". The Journal of Pharmacy and Pharmacology
Curcuma_zedoaroides
Reaction in organic chemistry
contrast to the Robinson synthesis, it does not employ dialdehydes like succinaldehyde or glutaraldehyde but simpler aldehydes like benzaldehyde. Therefore
Petrenko-Kritschenko piperidone synthesis
Petrenko-Kritschenko_piperidone_synthesis
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