2,1,3-Benzothiadiazole | CAS:273-13-2
2,1,3-Benzothiadiazole
- 名称:2,1,3-苯并噻二唑 | 2,1,3-Benzothiadiazole
- CAS号:273-13-2
- 别名:Piazthiole; Benzo-2,1,3-thiadiazole
- 分子式:C6H4N2S
- 分子量:136.17
- EINESC号:205-985-2
产品描述
物理化学性质
熔点 | 42-44 ºC |
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沸点 | 206-206 ºC |
闪点 | 203 ºF |
安全数据
安全说明书 | S24/25 |
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SDS
来源 | SDS样本 |
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没有数据 | 没有数据 |
产品合成路线
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15N chemically induced dynamic nuclear polarization during reaction of N-acetyl-L-tyrosine with the nitrating systems nitrite/hydrogen peroxide/horseradish peroxidase and nitrite/hypochloric acid.M Lehnig Archives of biochemistry and biophysics, 393(2), 245-254 (2001-09-15)
Chlorine dioxide oxidations of tyrosine, N-acetyltyrosine, and dopa.Michael J Napolitano et al.Chemical research in toxicology, 18(3), 501-508 (2005-03-22)
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Solution interactions between the uranyl cation [UO2(2+)] and histidine, N-acetyl-histidine, tyrosine, and N-acetyl-tyrosine.Wei Xie et al.Journal of inorganic biochemistry, 103(1), 58-63 (2008-10-25)
Chlorination of N-acetyltyrosine with HOCl, chloramines, and myeloperoxidase-hydrogen peroxide-chloride system.G Drabik et al.Acta biochimica Polonica, 48(1), 271-275 (2001-07-07)
Utilization of tyrosine-containing dipeptides and N-acetyl-tyrosine in hepatic failure.W Druml et al.Hepatology (Baltimore, Md.), 21(4), 923-928 (1995-04-01)
Isolation and analysis of dityrosine from enzyme-catalyzed oxidation of tyrosine and X-irradiated peptide and proteins.M Sharma et al.Chemico-biological interactions, 108(3), 171-185 (1998-04-07)
Detection of autosomal dominant polycystic kidney disease by NMR spectroscopic fingerprinting of urine.Wolfram Gronwald et al.Kidney international, 79(11), 1244-1253 (2011-03-11)
Neutrophils employ the myeloperoxidase system to generate antimicrobial brominating and chlorinating oxidants during sepsis.J P Gaut et al.Proceedings of the National Academy of Sciences of the United States of America, 98(21), 11961-11966 (2001-10-11)
Influence of alkyl group on amide nitrogen atom on fluorescence quenching of tyrosine amide and N-acetyltyrosine amide.Justyna Mrozek et al.Biophysical chemistry, 111(2), 105-113 (2004-09-24)
Influence of alkyl group on amide nitrogen atom on fluorescence quenching of tyrosine amide and N-acetyltyrosine amide.Justyna Mrozek et al.Biophysical chemistry, 111(2), 105-113 (2004-09-24)
Restrictive dermopathy: report of one case and the metabolic and post-mortem findings.Ming-Chou Chiang et al.The Turkish journal of pediatrics, 50(5), 492-494 (2008-12-24)
Formation of nitrating and chlorinating species by reaction of nitrite with hypochlorous acid. A novel mechanism for nitric oxide-mediated protein modification.J P Eiserich et al.The Journal of biological chemistry, 271(32), 19199-19208 (1996-08-09)
[Recording the delta-pH-generating biochemical reactions by light-addressed sensors with Ta2O5 dielectrics].A N Reshetilov et al.Doklady Akademii nauk, 342(5), 700-702 (1995-06-01)
Effect of 3-hydroxyanthranilic acid on mushroom tyrosinase activity.A Rescigno et al.Biochimica et biophysica acta, 1384(2), 268-276 (1998-07-11)
Horseradish peroxidase oxidation of tyrosine-containing peptides and their subsequent polymerization: a kinetic study.T Michon et al.Biochemistry, 36(28), 8504-8513 (1997-07-15)
Investigation of DNA-protein cross-link formation between lysozyme and oxanine by mass spectrometry.Hauh-Jyun Candy Chen et al.Chembiochem : a European journal of chemical biology, 9(7), 1074-1081 (2008-03-21)
Exploring photoreactions between polyazaaromatic Ru(II) complexes and biomolecules by chemically induced dynamic nuclear polarization measurements.Sandrine Perrier et al.Journal of the American Chemical Society, 131(34), 12458-12465 (2009-08-08)
N-acetyl-L-tyrosine (NAT) as a substrate for mushroom tyrosinase.V Kahn et al.Pigment cell research, 11(1), 24-33 (1998-04-02)
N-Glycans protect proteins from protease digestion through their binding affinities for aromatic amino acid residues.T Nishiyama et al.Journal of biochemistry, 127(3), 427-433 (2000-03-25)
Evidence for rapid inter- and intramolecular chlorine transfer reactions of histamine and carnosine chloramines: implications for the prevention of hypochlorous-acid-mediated damage.David I Pattison et al.Biochemistry, 45(26), 8152-8162 (2006-06-28)
N-acetyl tyrosyluria caused by parenteral or enteral administration of N-acetyl-L-tyrosine: differentiation from hereditary and acquired tyrosinemias.Stanley H Korman et al.Journal of pediatric gastroenterology and nutrition, 39(1), 95-100 (2004-06-10)
Surfactants, aromatic and isoprenoid compounds, and fatty acid biosynthesis inhibitors suppress Staphylococcus aureus production of toxic shock syndrome toxin 1.Peter J McNamara et al.Antimicrobial agents and chemotherapy, 53(5), 1898-1906 (2009-02-19)
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Kinetic evidence for the formation of a Michaelis-Menten-like complex between horseradish peroxidase compound II and di-(N-acetyl-L-tyrosine).W Wang et al.The Biochemical journal, 340 ( Pt 1), 329-336 (1999-05-07)
N-acetyl-L-tyrosine as a tyrosine source in adult parenteral nutrition.L John Hoffer et al.JPEN. Journal of parenteral and enteral nutrition, 27(6), 419-422 (2003-11-19)
Application of chemically induced dynamic nuclear polarization to the nitration of N-acetyltyrosine and to some reactions of peroxynitrite.A R Butler et al.Nitric oxide : biology and chemistry, 4(5), 472-482 (2000-10-06)
Reactions of hypochlorous acid with tyrosine and peptidyl-tyrosyl residues give dichlorinated and aldehydic products in addition to 3-chlorotyrosine.S Fu et al.The Journal of biological chemistry, 275(15), 10851-10858 (2001-02-07)
Synthesis and evaluation of N-acetyl-L-tyrosine based compounds as PPARalpha selective activators.Rakesh Kumar et al.European journal of medicinal chemistry, 42(4), 503-510 (2006-12-26)
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Products protected by valid patents are not offered for sale in countries where the sale of such products constitutes a patent infringement and its liability is at buyer's risk.
Products currently covered by valid US Patents are offered for R&D use in accordance with 35 USC 271 +A13(1).
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