CAS 298-12-4
:Ácido glioxílico
Descripción:
Ácido glioxílico, con el número CAS 298-12-4, es un compuesto orgánico simple caracterizado por su estructura como un compuesto dicarbonílico, que presenta tanto un grupo funcional aldehído como un grupo funcional ácido carboxílico. Es un líquido incoloro a amarillo pálido con un olor penetrante y es altamente soluble en agua, lo que lo convierte en un reactivo versátil en varias reacciones químicas. Ácido glioxílico es conocido por su reactividad, particularmente en reacciones de condensación, y se utiliza a menudo en la síntesis de varios compuestos orgánicos, incluidos aminoácidos y productos farmacéuticos. También puede actuar como agente reductor y está involucrado en la formación de derivados de glioxilato. En términos de seguridad, Ácido glioxílico se considera peligroso, con posibles efectos irritantes en la piel, los ojos y el sistema respiratorio, lo que requiere precauciones adecuadas en su manejo. Sus aplicaciones se extienden a los campos de la bioquímica, la agricultura y la producción de colorantes y fragancias, destacando su importancia tanto en entornos industriales como de laboratorio.
Fórmula:C2H2O3
InChI:InChI=1/C2H2O3/c3-1-2(4)5/h1H,(H,4,5)/p-1
Clave InChI:InChIKey=HHLFWLYXYJOTON-UHFFFAOYSA-N
SMILES:C(C=O)(O)=O
Sinónimos:- 2-Oxoacetic acid
- Acetic acid, 2-oxo-
- Acide glyoxylique
- Acido Glioxilico
- Carboxyformaldehyde
- Formylcarboxylic acid
- Formylformic acid
- Glyoxalic acid
- Glyoxo High Pure 50
- Glyoxylic Acid
- Glyoxylsaeure
- Glyoxylsaure
- Nsc 27785
- Oxalaldehydic acid
- Oxoacetic acid
- Oxoethanoic acid
- α-Ketoacetic acid
- Acetic acid, oxo-
- Glyoxalate
- glyoxylate
- oxoacetate
- Aldehydoformicacid
- 2-Oxoethanoic Acid
- oxo-acetic acid
- Formic acid, formyl-
- Formylformic
- glyoxylicacid(50%orless)
- formyl-formicaci
- alpha-ketoaceticacid
- oxo-aceticaci
- GA
- oxalaldehydicacid
- OCHCOOH
- alpha-Ketoacetic acid
- kyselinaglyoxylova
- Kyselina glyoxylova
- Ver más sinónimos
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Encontrado 11 productos.
Glyoxylic Acid (ca. 50% in Water, ca. 9mol/L)
CAS:Fórmula:C2H2O3Forma y color:Colorless to Light orange to Yellow clear liquidPeso molecular:74.04Glyoxylic acid, 50% w/w aq. soln.
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 Sci
Fórmula:C2H2O3Forma y color:Clear colorless to yellow, LiquidPeso molecular:74.04Glyoxylic acid solution, 50% in water
CAS:Fórmula:C2H2O3Pureza:%Forma y color:LiquidPeso molecular:74.0355Glyoxylic acid, 50% in water
CAS:Fórmula:OHCCO2HForma y color:Colourless to light yellow liquidPeso molecular:74.04Glyoxalic acid
CAS:Glyoxalic acid is an organic compound. It is both an aldehyde and a carboxylic acid.Fórmula:C2H2O3Forma y color:SoildPeso molecular:74.04Glyoxylic acid (ca. 50% in Water, ca. 9mol/L)
CAS:Pureza:95.0%Forma y color:LiquidPeso molecular:74.03500366210938Glyoxylic Acid (50% aqueous solution)
CAS:Applications Glyoxylic Acid is used as a reagent in the synthesis of N-{[6-chloro-4-(2,6-dimethoxyphenyl)quinazolin-2-yl]carbonyl}-L-leucine, a novel nonpeptide chemotype selective for neurotensin receptor 2. Also used as a reagent in the synthesis of elemonic acid derivatives as Pin1 inhibitors.
References Thomas, J.B., et al.: Bioorg. Med. Chem. Lett., 25, 292 (2015); Li, X., et al.: Bioorg. Med. Chem. Lett., 24, 5612 (2014)Fórmula:C2H2O3Forma y color:Colourless LiquidPeso molecular:74.04Glyoxylic acid - 50% aqueous solution
CAS:Glyoxylic acid is a dicarboxylic acid that can be found in the human body. It is oxidized to glyoxylate, which is then converted to oxalate by enzymes. Glyoxylic acid is a product of glycolysis, and has been shown to have antioxidant properties. Glyoxylic acid has been shown to inhibit the production of peptide hormones such as ACTH and TRH, as well as infectious diseases such as AIDS and malaria. It also has an effect on biochemical properties such as the redox potentials. The optimum extraction process for this compound is by ion-exchange chromatography with aqueous solvent. X-ray diffraction data can be used to identify this compound. The reaction mechanism for glyoxylic acid involves two steps: oxidation at carbon 2 followed by elimination at carbon 3. This chemical can be detected using analytical methods such as spectrophotometry or x-ray photoelectron spectroscopy (XPSFórmula:C2H2O3Pureza:Min. 95%Forma y color:Clear LiquidPeso molecular:74.04 g/mol
