CAS 936-02-7: Salicylic acid, hydrazide
Formula:C7H8N2O2
InChI:InChI=1S/C7H8N2O2/c8-9-7(11)5-3-1-2-4-6(5)10/h1-4,10H,8H2,(H,9,11)
InChI key:InChIKey=XSXYESVZDBAKKT-UHFFFAOYSA-N
SMILES:C(NN)(=O)C1=C(O)C=CC=C1
Synonyms:- 2-Hydroxybenzene-1-carbohydrazide
- 2-Hydroxybenzene-1-carbohydrazonic acid
- 2-Hydroxybenzenecarboxylic acid hydrazide
- 2-Hydroxybenzhydrazide
- 2-Hydroxybenzohydrazide
- 2-Hydroxybenzoic acid hydrazide
- 2-Hydroxybenzoic hydrazide
- 2-Hydroxybenzoyl hydrazide
- 2-Hydroxybenzoylhydrazine
- Benzoic acid, 2-hydroxy-, hydrazide
- NSC 652
- See more synonyms
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Found 8 products.
2-Hydroxybenzhydrazide, 98+%
CAS:This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.Formula:C7H8N2O2Purity:98+%Color and Shape:White to cream or pale brown, Crystalline powderMolecular weight:152.15Salicyl Hydrazide
CAS:Formula:C7H8N2O2Purity:>98.0%(T)(HPLC)Color and Shape:White to Almost white powder to crystalMolecular weight:152.15Salicylhydrazide, 98+%
CAS:This Thermo Scientific Chemicals brand product was originally part of the Acros Organics product portfolio. Some documentation and label information may refer to the legacy brand. The original Acros Organics product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.Formula:C7H8N2O2Purity:98+%Color and Shape:Crystalline powder, White to beige to light brownMolecular weight:152.15Salicylhydrazide
CAS:Salicylic hydrazide is a coumarin derivative that is used as a hypoglycemic agent. It has been shown to have anti-cancer properties in colorectal adenocarcinoma cells and also has synergistic effects with the fluorescence probe DNP (2,4-dinitrophenylhydrazine). Salicylic hydrazide can be synthesized from salicylaldehyde and hydrazine monohydrate. The reaction mechanism proceeds via an intramolecular hydrogen bond between the hydroxyl group of salicylic acid and the amine group of hydrazine. Salicylic hydrazide also has been found to increase human serum glucose levels by inhibiting gluconeogenesis. It does this by catalyzing the conversion of pyruvic acid to lactic acid, which inhibits the enzyme pyruvate carboxykinase (PCK), thereby halting gluconeogenesis. The analytical method for determining salicylic hydrazFormula:C7H8N2O2Purity:Min. 95%Color and Shape:PowderMolecular weight:152.15 g/mol
