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Phthalazine | CAS:253-52-1
Phthalazine
  • Name:Phthalazine
  • CAS:253-52-1
  • Synonyms:2,3-Benzodiazine
  • Molecular Formula:C8H6N2
  • Molecular Weight:130.15
  • EINESC:205-963-2

Description

Properties

Melting point 88-92 ºC
Boiling point 315-317 ºC

Safety

SDS/MSDS S24/25

SDS

Source SDS/MSDS Samples
没有数据没有数据
Synthetic Route
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Articles
Peer-Reviewed Papers
On the decarboxylation of 2-methyl-1-tetralone-2-carboxylic acid-oxidation of the enol intermediate by triplet oxygen.Riahi A, et al. New. J. Chem., 37(8), 2245-2249 (2013) Nickel-catalyzed asymmetric α-arylation and heteroarylation of ketones with chloroarenes: effect of halide on selectivity, oxidation state, and room-temperature reactions.Shaozhong Ge et al.Journal of the American Chemical Society, 133(41), 16330-16333 (2011-09-16) Application of [hydroxy(tosyloxy)iodo]benzene in the Wittig-ring expansion sequence for the synthesis of beta-benzocyclo-alkenones from alpha-benzocycloalkenones.Michael W Justik et al.Molecules (Basel, Switzerland), 10(1), 217-225 (2007-11-17) Heck-type reactions of allylic alcohols: Part IV:(2-Substituted)-1-indanones via 5-endo-trig cyclizations.Zawisza AM, et al. J. Mol. Catal. A: Chem., 283(1), 140-145 (2008) Cyclophanes. 9. anti-[2.2](2, 6) Azulenophane. Synthesis and charge-transfer interaction.Luhowy R and Keehn PM. Journal of the American Chemical Society, 99(11), 3797-3805 (1977) Recent advances in enzymatic and chemical deracemisation of racemic compounds.Michał Rachwalski et al.Chemical Society reviews, 42(24), 9268-9282 (2013-09-26) Toward chemistry-based design of the simplest metalloenzyme-like catalyst that works efficiently in water.Taku Kitanosono et al.Chemistry, an Asian journal, 10(1), 133-138 (2014-10-29) The O-acylation of ketone enolates by allyl 1H-imidazole-1-carboxylate mediated with boron trifluoride etherate: a convenient procedure for the synthesis of substituted allyl enol carbonates.Barry M Trost et al.The Journal of organic chemistry, 72(24), 9372-9375 (2007-10-30) Selective and easy preparation of enol carbonates of α-disubstituted aryl ketones from their lithium enolates.Aboulhoda SJ, et al. Tetrahedron Letters, 36(27), 4795-4796 (1995) Amino alcohol-mediated enantioselective syntheses of α-substituted indanones and tetralones, ammonium enolates as key intermediates.Muzart J. Tetrahedron Asymmetry, 25(9), 697-704 (2014) Structural effects in the Pd-induced enantioselective deprotection-decarboxylation of β-ketoesters.Kukula P, et al. Tetrahedron Asymmetry, 18(24), 2859-2868 (2007)
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