CAS 1574-10-3
:Benzaldehyde, semicarbazone
Description:
Benzaldehyde semicarbazone is an organic compound formed from the reaction of benzaldehyde and semicarbazide. It is characterized by its white crystalline appearance and is typically used in organic synthesis and as a reagent in various chemical analyses. The compound features a semicarbazone functional group, which is derived from the condensation of a carbonyl compound (in this case, benzaldehyde) with semicarbazide. Benzaldehyde semicarbazone is known for its moderate solubility in polar solvents like ethanol and water, while being less soluble in non-polar solvents. It exhibits stability under standard conditions but can undergo hydrolysis in the presence of strong acids or bases. The compound is often utilized in the identification and characterization of aldehydes and ketones due to its ability to form derivatives that can be easily analyzed. Additionally, it has applications in the field of medicinal chemistry and can serve as a precursor for the synthesis of various pharmaceuticals. Safety precautions should be taken when handling this compound, as it may pose health risks if ingested or inhaled.
Formula:C8H9N3O
InChI:InChI=1S/C8H9N3O/c9-8(12)11-10-6-7-4-2-1-3-5-7/h1-6H,(H3,9,11,12)
InChI key:InChIKey=AKGUXECGGCUDCV-UHFFFAOYSA-N
SMILES:C(=NNC(N)=O)C1=CC=CC=C1
Synonyms:- (Benzylideneamino)urea
- 1-Benzylidenesemicarbazide
- 2-(Phenylmethylene)hydrazinecarboxamide
- 2-Benzylidenehydrazinecarboxamide
- 3-Hydroxybenzaldehyde semicarbazone
- Ai3-03680
- Benzylidenesemicarbazide
- Hydrazinecarboxamide, 2-(phenylmethylene)-
- Nsc 1591
- Benzaldehyde semicarbazone
- Benzaldehyde, semicarbazone
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Found 3 products.
2-Benzylidenehydrazinecarboxamide
CAS:Formula:C8H9N3OPurity:97%Color and Shape:SolidMolecular weight:163.1766Benzaldehyde Semicarbazone
CAS:Formula:C8H9N3OColor and Shape:White To Off-WhiteMolecular weight:163.18Benzaldehyde semicarbazone
CAS:<p>Benzaldehyde semicarbazone is a hydrogen bond acceptor and donor, which can be used for the synthesis of pharmaceuticals. It is also known to have significant biological activity, including anticonvulsant activity. Benzaldehyde semicarbazone has been shown to be an inhibitor of pyrazole ring formation in the reaction between 4-chlorobenzaldehyde oxime and hydrochloric acid. This inhibition may be due to its ability to act as a hydrogen bond acceptor, forming hydrogen bonds with both the carbonyl group of 4-chlorobenzaldehyde oxime and the protonated chloride ion. The mechanism is supported by kinetic studies which show that benzaldehyde semicarbazone has a much lower activation energy than the other reactants involved in the reaction.</p>Formula:C8H9N3OPurity:Min. 95%Color and Shape:PowderMolecular weight:163.18 g/mol


