Carbazochrome

CAS : 69-81-8

Ref. TR-C175820

Informations sur le produit

• Nom: Carbazochrome
• Synonymes: Adenochrome semicarbazone, Hydrazinecarboxamide, 2-(1,2,3,6-tetrahydro-3-hydroxy-1-methyl-6-oxo-5H-indol-5-ylidene)-, 5,6-Indolinedione, 3-hydroxy-1-methyl-, 5-semicarbazone (7CI,8CI), Adrenochrome semicarbazone (6CI), 2-(1,2,3,6-Tetrahydro-3-hydroxy-1-methyl-6-oxo-5H-indol-5-ylidene)hydrazinecarboxamide, 3-Hydroxy-1-methyl-5,6-indolindione 5-semicarbazone, Adchnon, Adedolon, Adrenochrome monosemicarbazone, Adrenostazin, Adrenoxyl, Adrezon, Adrokson, Adroxon, Carbazochrom, Cartabes, Cromadrenal, Cromosil, NSC 73742, Sangostasin, Sangostazin, (5Z)-3-hydroxy-1-methyl-2,3-dihydro-1H-indole-5,6-dione 5-semicarbazone, 2-(3-Hydroxy-1-methyl-6-oxo-2,3-dihydro-1H-indol-5(6H)-ylidene)hydrazinecarboxamide, 3-hydroxy-1-methyl-2,3-dihydro-1H-indole-5,6-dione 5-semicarbazone, 5,6-Indolinedione, 3-hydroxy-1-methyl-, 5-semicarbazone, Adrenochrome Monosemicarbazone, Hydrazinecarboxamide, 2-(1,2,3,6-tetrahydro-3-hydroxy-1-methyl-6-oxo-5H-indol-5-ylidene)-

Description

Stability Hygroscopic
Applications Carbazochrome is an oxidation product of Epinephrine [E588580]) that improves microcirculatory tone. Derivatives such as carbazochrome salicylate and carbazochrome sodium sulfonate, are used as hemostats and treatment to prevent dengue shock syndrome, respectively.
References Basile, M., et al.: Curr. Ther. Res., 63, 527 (2002); McLean, W. & Campolongo, J.: Can. J. Surg., 16, 333 (1973); Tassniyom, S., et al.: J. Ped., 131, 525 (1997)

• Marque: TRC

Propriétés chimiques

• Masse moléculaire: 236.23
• Formule: C₁₀H₁₂N₄O₃
• Couleur/Forme: Neat
• InChI: InChI=1S/C10H12N4O3/c1-14-4-9(16)5-2-6(12-13-10(11)17)8(15)3-7(5)14/h2-3,9,16H,4H2,1H3,(H3,11,13,17)/b12-6-
• Code InChI: InChIKey=XSXCZNVKFKNLPR-SDQBBNPISA-N
• SMILES: CN1CC(O)C2=C/C(=N/NC(N)=O)C(=O)C=C21