CAS: 6495-46-1; Dexoxadrol

该化合物是属于二氧化物类的化学化合物,其特点是循环醚结构,通常包括五人环中的两个氧原子.二氧化物因其独特的反应能力和参与化学转化的能力,在各个领域,包括制药和有机合成领域的潜在应用而闻名.该化合物外观一般没有色,面貌苍白,可能具有独特的气味.其溶解性性常允许其在有机溶剂中溶解,使其在各种化学过程中有用.安全数据表明,与许多有机化合物一样,它应该谨慎处理,因为如果吸入或摄取,它可能会对健康造成危害.

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MSDS等安全信息

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      专利信息


      专利号:US-2008214827-A1
      优先权日:2004-02-03
      标 题:Synthesis of Cyanoimino-Benzoimidazoles
      发明人:GOEHRING R RICHARD; WHITEHEAD JOHN; SHAO BIN
      权利人:EURO CELTIQUE SA
      摘要:Disclosed in certain embodiments is a process for synthesizing a compound of formula (V) and salts thereof.

      专利号:WO-2005075459-A1
      优先权日:2004-02-03
      标题:Synthesis of cyanoimino-benzoimidazoles

      专利号:EP-1711484-A4
      优先权日:2004-02-03
      标题:SYNTHESIS OF CYANOIMINO-BENZOIMIDAZOLES

      专利号:EP-1711484-A1
      优先权日:2004-02-03
      标 题:Synthesis of cyanoimino-benzoimidazoles

      专利号:US-2014315720-A1
      优先权日:2012-10-24
      标 题 :Polysaccharide ester microspheres and methods and articles relating thereto
      发明人:FALLON DENIS G; GARRETT THOMAS S; KIZER LAWTON E; ZAZZARA KAREN L; COMBS MICHAEL T; JOHNSON RICHARD K; DEHART GARY
      权利人:CELANESE ACETATE LLC
      摘要:A method for producing a polysaccharide ester microsphere may include forming a polysaccharide ester product from a polysaccharide synthesis, wherein the polysaccharide ester product comprises a polysaccharide ester and a solvent; diluting the polysaccharide ester product, thereby yielding a polysaccharide ester dope; and forming a plurality of polysaccharide ester microspheres from the polysaccharide ester dope. Suitable polysaccharides may include, but are not limited to, starch, cellulose, hemicellulose, algenates, chitosan, and any combination thereof. Esters thereof may be organic esters (e.g., acetate and the like), inorganic esters (e.g., sulfonates and the like), or combinations thereof. Further, the solids conent of the polysaccharide ester dope, in some instances, may be greater than about 16 wt %.

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      ✅ COA系统入驻 | 共享模式

      主要参考文献


      1: Banerjee A, Schepmann D, Wünsch B. Synthesis and NMDA receptor affinity of fluorinated dioxadrol analogues. Bioorg Med Chem. 2010 Jun 1;18(11):4095-102. doi: 10.1016/j.bmc.2010.04.002. Epub 2010 Apr 4. 5(6):273-80. 243(1):110-7. 263(1-2):115-20. doi: 10.1016/0014-2999(94)90531-2. 254(3):952-6. 307(1-2):85-90. doi: 10.1016/0006-8993(84)90463-3. 33(22):3529-35. doi: 10.1016/0006-2952(84)90133-3.
      55:90-6. 5(4-6):253-6. doi: 10.1016/0143-4179(85)90026-5. 9(11):4051-61. doi: 10.1523/JNEUROSCI.09-11-04051.1989.

      合成参考文献


      参考文献:10.1016/0006-291x(85)90206-2
      摘要:Haring R, Kloog Y, Sokolovsky M. Regional heterogeneity of rat brain phencyclidine (PCP) receptors revealed by photoaffinity labeling with [3H] azido phencyclidine. Biochemical and Biophysical Research Communications. 1985 Sep;131(3):1117–23. doi: 10.1016/0006-291x(85)90206-2.
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