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Glutaroyl dichloride | CAS:2873-74-7
Glutaroyl dichloride
  • Name:Glutaroyl dichloride
  • CAS:2873-74-7
  • Synonyms:1,5-Pentanedioyl chloride; 5-Chloro-5-oxopentanoyl chloride; Glutaric acid dichloride; Glutaroyl chloride; Glutaryl dichloride; NSC 519867
  • Molecular Formula:C5H6Cl2O2
  • Molecular Weight:169.01
  • EINESC:220-711-1

Description

Properties

Boiling point 217 ºC**
Flash point 106.7±0.0 ºC, 计算值*
Density 1.319±0.06 g/cm3 (20 º
Refractive index 1.4706 (20 ºC)***

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Peer-Reviewed Papers
Cinnabarinic acid was formed in damaged mitochondria and its effect on mitochondrial respiration.Y Nagamura et al.Advances in experimental medicine and biology, 467, 419-423 (2000-03-18) 3-Hydroxyanthranilic acid-derived compounds formed through electrochemical oxidation.H Iwahashi Journal of chromatography. B, Biomedical sciences and applications, 736(1-2), 237-245 (2000-02-17) Mechanism of reaction of 3-hydroxyanthranilic acid with molecular oxygen.M K Manthey et al.Biochimica et biophysica acta, 1034(2), 207-212 (1990-05-16) Laccase-catalyzed formation of cinnabarinic acid is responsible for antibacterial activity of Pycnoporus cinnabarinus.C Eggert Microbiological research, 152(3), 315-318 (1997-11-14) Oxidative reactivity of the tryptophan metabolites 3-hydroxyanthranilate, cinnabarinate, quinolinate and picolinate.J A Dykens et al.Biochemical pharmacology, 36(2), 211-217 (1987-01-15) Aminophenoxazinones as inhibitors of indoleamine 2,3-dioxygenase (IDO). Synthesis of exfoliazone and chandrananimycin A.Raffaele Pasceri et al.Journal of medicinal chemistry, 56(8), 3310-3317 (2013-03-26) Oxidation of 3-hydroxyanthranilic acid to the phenoxazinone cinnabarinic acid by peroxyl radicals and by compound I of peroxidases or catalase.S Christen et al.Biochemistry, 31(34), 8090-8097 (1992-09-01) Development of a fluorimetric detection method for cinnabarinic acid using ortho-tolyl hydrazine as the derivatization reagent.Hideaki Iizuka et al.Biomedical chromatography : BMC, 24(3), 231-234 (2009-07-25) Novel interaction between laccase and cellobiose dehydrogenase during pigment synthesis in the white rot fungus Pycnoporus cinnabarinus.U Temp et al.Applied and environmental microbiology, 65(2), 389-395 (1999-01-30) Superoxide dismutase enhances the formation of hydroxyl radicals in the reaction of 3-hydroxyanthranilic acid with molecular oxygen.H Iwahashi et al.The Biochemical journal, 251(3), 893-899 (1988-05-01) Cinnabarinate formation in malpighian tubules of the silkworm. Bombyx mori: reaction mechanism of cinnabarinate formation in the presence of catalase and manganese ions.H Ogawa et al.Hoppe-Seyler's Zeitschrift fur physiologische Chemie, 364(11), 1507-1518 (1983-11-01) Laccase-mediated formation of the phenoxazinone derivative, cinnabarinic acid.C Eggert et al.FEBS letters, 376(3), 202-206 (1995-12-04) Simultaneous determination of 3-hydroxyanthranilic and cinnabarinic acid by high-performance liquid chromatography with photometric or electrochemical detection.S Christen et al.Analytical biochemistry, 200(2), 273-279 (1992-02-01) Cinnabarinic acid formation in Malpighian tubules of the silkworm, Bombyx mori. Participation of catalase in cinnabarinic acid formation in the presence of manganese ion.H Ogawa et al.Hoppe-Seyler's Zeitschrift fur physiologische Chemie, 364(8), 1059-1066 (1983-08-01) Cinnabarinic acid, an endogenous agonist of type-4 metabotropic glutamate receptor, suppresses experimental autoimmune encephalomyelitis in mice.Fazio F, et al. Neuropharmacology, 81, 237-243 (2014)
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