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oxalyl

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oxalyl
oxalyl Chem. (ˈɒksəlɪl) [f. oxal- + -yl.] The hypothetical radical (C2O2) of oxalic acid.1859 Fownes Man. Chem. 398 One molecule of C4H4 (ethylene) and C4O4 (oxalyl). 1873 C. H. Ralfe Phys. Chem. p. xxi, Oxalic acid, C2H2O4, is a double molecule of water in which half the hydrogen is replaced by oxa... Oxford English Dictionary
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Oxalyl dicyanide
Oxalyl dicyanide is a chemical compound with the formula C4N2O2. Formation Oxalyl dicyanide can be formed by the hydrolysis of diiminosuccinonitrile. wikipedia.org
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Oxalyl fluoride
This colorless liquid is prepared by reaction of sodium fluoride with oxalyl chloride. See also Oxalyl chloride Oxalyl bromide Dioxane tetraketone Oxalyl References Acyl fluorides Inorganic carbon compounds Carbon oxohalides wikipedia.org
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Oxalyl-CoA decarboxylase
The systematic name of this enzyme class is oxalyl-CoA carboxy-lyase (formyl-CoA-forming). Other names in common use include oxalyl coenzyme A decarboxylase, and oxalyl-CoA carboxy-lyase. wikipedia.org
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Oxalyl chloride
Oxalyl chloride is an organic chemical compound with the formula . Oxalyl chloride is produced commercially from ethylene carbonate. wikipedia.org
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Oxalate—CoA ligase
of this enzyme are ATP, oxalate, and coenzyme A (CoA), whereas its 3 products are AMP, diphosphate, and oxalyl-CoA. Other names in common use include oxalyl-CoA synthetase, and oxalyl coenzyme A synthetase. wikipedia.org
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Oxalate CoA-transferase
In enzymology, an oxalate CoA-transferase () is an enzyme that catalyzes the chemical reaction succinyl-CoA + oxalate succinate + oxalyl-CoA Thus, the two substrates of this enzyme are succinyl-CoA and oxalate, whereas its two products are succinate and oxalyl-CoA. wikipedia.org
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Oxalate degrading enzyme
Oxalyl-CoA decarboxylasemainly mediates degradation of bacterial oxalic acid. Formyl-CoA transferase mediates the exchange of oxalyl and formyl groups on coenzyme A, interconverting formyl-CoA and oxalyl-CoA. wikipedia.org
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Acyl cyanide
Examples include acetyl cyanide, formyl cyanide, and oxalyl dicyanide. Acyl cyanides are reagents in organic synthesis. wikipedia.org
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Carbon oxohalide
They include carbonyl halides, , and oxalyl halides, , where X = F, Cl, Br or I. wikipedia.org
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Oxalic anhydride
It has been conjectured to be a fleeting intermediate in the thermal decomposition of certain oxalates and certain chemoluminescent reactions of oxalyl wikipedia.org
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2,3-diaminopropionate N-oxalyltransferase
CoA + N3-oxalyl-L-2,3-diaminopropanoate Thus, the two substrates of this enzyme are oxalyl-CoA and L-2,3-diaminopropanoate, whereas its two products are CoA and N3-oxalyl-L-2,3-diaminopropanoate. wikipedia.org
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Tetrahydroxy-1,4-benzoquinone bisoxalate
It was obtained by reacting tetrahydroxy-1,4-benzoquinone with oxalyl chloride in tetrahydrofuran. wikipedia.org
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Glyoxylate dehydrogenase (acylating)
In enzymology, a glyoxylate dehydrogenase (acylating) () is an enzyme that catalyzes the chemical reaction glyoxylate + CoA + NADP+ oxalyl-CoA + NADPH + H+ The 3 substrates of this enzyme are glyoxylate, CoA, and NADP+, whereas its 3 products are oxalyl-CoA, NADPH, and H+. wikipedia.org
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Thiocarbonic acid
Oxalyl chloride gives oxalyl trithiocarbonate (). Applications Thiocarbonic acid currently has no significant applications. wikipedia.org
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