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semicarbazone
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Semicarbazone - Wikipedia
A semicarbazone is a derivative of imines formed by a condensation reaction between a ketone or aldehyde and semicarbazide.
en.wikipedia.org
en.wikipedia.org
Illustrated Glossary of Organic Chemistry - Semicarbazone
Semicarbazone: A functional group containing the moiety shown below, or a molecule containing this functional group. General semicarbazone molecular ...
www.chem.ucla.edu
www.chem.ucla.edu
Semicarbazone - an overview | ScienceDirect Topics
Semicarbazone is defined as a derivative formed by the reaction of a ketone with semicarbazide, resulting in a solid that can be isolated and characterized ...
www.sciencedirect.com
www.sciencedirect.com
semicarbazone
semicarbazone Chem. (sɛmɪˈkɑːbəzəʊn) [f. prec. + -one.] Any of a class of (usu. crystalline) compounds of general formula RR{p}C:N·NH·CO·NH2 which are prepared by the condensation of semicarbazide with carbonyl compounds, in order to characterize the parent carbonyl or to protect the carbonyl group ...
Oxford English Dictionary
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Synthesis and Antibacterial Activity of Novel Hydroxy ...
The general structure of the active (thio) semicarbazones is disclosed in Figure 1, which consists of an aromatic system linked to the (thio) semicarbazone ...
pmc.ncbi.nlm.nih.gov
pmc.ncbi.nlm.nih.gov
ACETONE SEMICARBAZONE AldrichCPR - Sigma-Aldrich
ACETONE SEMICARBAZONE AldrichCPR; CAS Number: 110-20-3; Linear Formula: C4H9N3O at Sigma-Aldrich.
www.sigmaaldrich.com
www.sigmaaldrich.com
A review of semicarbazone-derived metal complexes for application ...
The review highlights the general methods of synthesizing semicarbazones, emphasizing their versatility and wide applicability in various ...
www.sciencedirect.com
www.sciencedirect.com
Pinacolone Semicarbazone | C7H15N3O | CID 4318256 - PubChem
Pinacolone Semicarbazone | C7H15N3O | CID 4318256 - structure, chemical names, physical and chemical properties, classification, patents, literature, ...
pubchem.ncbi.nlm.nih.gov
pubchem.ncbi.nlm.nih.gov
A QUANTITATIVE STUDY OF SEMICARBAZONE FORMATION
This article is cited by 101 publications. Francis L. C. Morgan, Ivo A. O. Beeren, Jurica Bauer, Lorenzo Moroni, Matthew B. Baker.
pubs.acs.org
pubs.acs.org
Semicarbazone Derivative of an Aldehyde/Ketone (Prepared by ...
Lynn El-Zoghby prepared this video of the Synthesis of Semicarbazone Derivative of an Aldehyde/Ketone. #OrganicStructureDetermination #TrEd #
www.youtube.com
www.youtube.com
General Acid Catalysis of Semicarbazone Formation
General Acid Catalysis of Semicarbazone Formation. Click to copy article linkArticle link copied! · Journal of the American Chemical Society · Article Views.
pubs.acs.org
pubs.acs.org
Carbazochrome
Mechanism of action
Carbazochrome, the semicarbazone of adrenochrome, that interacts with α-adrenoreceptors on surface of platelets, which are coupled
wikipedia.org
en.wikipedia.org
nitrofurazone
nitrofurazone Pharm. (naɪtrəʊˈfɜːrəzəʊn) [f. nitro- + furfuraldehyde + semicarbazone in the chemical name of the compound, 5-nitrofurfuraldehyde semicarbazone.] A yellow crystalline cyclic compound, C6H6N4O4, which is an antibacterial agent used locally on burns, wounds, and skin infections, and in ...
Oxford English Dictionary
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2,3,4-Pentanetrione
2,3,4-pentanetrione-3-(O-methyloxime), 2,3,4-pentanetrione-2-oxime, 2,3,4-pentanetrione-2,3-dioxime, 2,3,4-pentanetrionetrioxime, 2,3,4-pentanetrione semicarbazone The 3-oxime melts at 75 °C and the bis(semicarbazone) has a melting point of 221 °C.
References
Triketones
Conjugated ketones
wikipedia.org
en.wikipedia.org
Bisthiosemicarbazone
A 'thiosemicarbazone' contains a sulfur atom in lieu of the ketonic oxygen in semicarbazone.
wikipedia.org
en.wikipedia.org