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(2R,2'R)-rel-2,2'-Bioxirane | CAS:298-18-0
(2R,2'R)-rel-2,2'-Bioxirane
  • Name:(2R,2'R)-rel-2,2'-Bioxirane
  • CAS:298-18-0
  • Synonyms:DL-1,2:3,4-Diepoxybutane; DL-Diepoxybutane; Rac-1,3-Butadiene diepoxide; dl-1,2:3,4-Diepoxybutane
  • Molecular Formula:C4H6O2
  • Molecular Weight:86.09
  • EINESC:206-060-6

Description

Properties

Melting point 3 ºC**
Boiling point 144 ºC**
Flash point 45.6±0.0 ºC, 计算值*
Density 1.383±0.06 g/cm3 (20 º

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Peer-Reviewed Papers
Synthesis, antimicrobial, and mosquito larvicidal activity of 1-aryl-4-methyl-3,6-bis-(5-methylisoxazol-3-yl)-2-thioxo-2,3,6,10b-tetrahydro-1H-pyrimido[5,4-c]quinolin-5-ones.E Rajanarendar et al.Bioorganic & medicinal chemistry letters, 20(20), 6052-6055 (2010-09-04) Synthesis and in vitro toxicity of hydroxylamine metabolites of sulfonamides.M J Rieder et al.The Journal of pharmacology and experimental therapeutics, 244(2), 724-728 (1988-02-01) Contribution of biotic and abiotic factors in the natural attenuation of sulfamethoxazole: A path analysis approach.Yan Li et al.The Science of the total environment, 633, 1217-1226 (2018-05-16) Evidence of superoxide radical contribution to demineralization of sulfamethoxazole by visible-light-driven Bi2O3/Bi2O2CO3/Sr6Bi2O9 photocatalyst.Shiyuan Ding et al.Journal of hazardous materials, 262, 812-818 (2013-10-22) Rapid degradation of sulphamethoxazole and the further transformation of 3-amino-5-methylisoxazole in a microbial fuel cell.Lu Wang et al.Water research, 88, 322-328 (2015-10-30) Synthesis of trans-1,3-diaryl-2-(5-methylisoxazol-3-yl)-2,3-dihydro-1H-naphtho[1,2-e][1,3]oxazines via bismuth(III)-catalyzed one-pot pseudo-four component reaction.Mehdi Shafiee et al.Molecular diversity, 16(4), 727-735 (2012-10-24) Biodegradation and metabolic pathway of sulfamethoxazole by Pseudomonas psychrophila HA-4, a newly isolated cold-adapted sulfamethoxazole-degrading bacterium.Benchao Jiang et al.Applied microbiology and biotechnology, 98(10), 4671-4681 (2014-02-14) Photo-Fenton oxidation of 3-amino-5-methylisoxazole: a by-product from biological breakdown of some pharmaceutical compounds.Bianca M Souza et al.Environmental science and pollution research international, 24(7), 6195-6204 (2015-11-12)
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