CAS: 6968-72-5; 3-(Hydroxymethyl)Pyridine 1-Oxide

该化合物是一种有机化合物,其特点是带有氢氧化硫组和N-氧化功能组的环状,其特征为:该化合物一般是无色的,可粉黄黄色液体或固态,视其形态和纯度而定;在水和极有机溶剂中溶解,可提高其在各种化学反应和应用中的效用;N-氧化物组的存在有助于其再活动,使其成为有机合成中的潜在中间体,特别是在制药和农用化学品的开发中.此外,该化合物可能展示生物活动,可以探索其潜在的治疗用途;在标准条件下,该化合物的稳定性便于在实验室环境中进行处理;与许多含氮的乙型循环一样,它可能参与氢的结合,影响它与其他分子的相互作用.应参考安全数据,以确保与所有化学物质一样,妥善处理和使用.

结构式图片

欧盟法规

ECHA物质C&L通报REACH预注册

上下游产品

3-hydroxymethylpyridin tetramethlyammonium chloride 3-(chloromethyl)pyridine N-oxide 3-Acetoxymethylpyridine-N-oxide 3-hydroxymethylpyridin 3-pyridinecarboxaldehyde

合成工艺路线路线简述

  • 合成目标产物 3-Pyridinemethanol N-Oxide 主要起始原料 3-Pyridinemethanol
  • (文献来源)合成步骤主要原料 3-Pyridinemethanol
📜3-吡啶甲醇置于间氯过氧苯甲酸体系中,用 氯仿 作为反应溶剂,化学反应 12.0H,以76%的收率获得产物3-吡啶甲醇氮氧化物
参考文献:Nagano,Hiroyuki; Nawata,Yoshiharu; Hamana,Masatomo,Chemical And Pharmaceutical Bulletin,1987,Vol. 35,# 10,P. 4068-4077
标题:Nagano,Hiroyuki; Nawata,Yoshiharu; Hamana,Masatomo,Chemical And Pharmaceutical Bulletin,1987,Vol. 35,# 10,P. 4068-4077

海关参考信息

专利信息


专利号:US-2004053999-A1
优先权日:1997-09-17
标题 :Novel compounds and methods for synthesis and therapy
发明人:BISCHOFBERGER NORBERT W; DAHL TERRENCE C; HITCHCOCK MICHAEL J M; KIM CHOUNG U; LEW WILLARD; LIU HONGTAO; MILLS ROGER G; WILLIAMS MATTHEW A
摘要:Novel compounds are described. The compounds generally comprise an acidic group, a basic group, a substituted amino or N-acyl and a group having an optionally hydroxylated alkane moiety. Pharmaceutical compositions comprising the inhibitors of the invention are also described. Methods of inhibiting neuraminidase in samples suspected of containing neuraminidase are also described. Antigenic materials, polymers, antibodies, conjugates of the compounds of the invention with labels, and assay methods for detecting neuraminidase activity are also described.

专利号:US-6225341-B1
优先权日:1995-02-27
标 题:Compounds and methods for synthesis and therapy
发明人:BISCHOFBERGER NORBERT W; KIM CHOUNG U; LEW WILLARD; LIU HONGTAO; WILLIAMS MATTHEW A
权利人:GILEAD SCIENCES INC
摘要:Novel compounds are described. The compounds generally comprise an acidic group, a basic group, a substituted amino or N-acyl and a group having an optionally hydroxylated alkane moiety. Pharmaceutical compositions comprising the inhibitors of the invention are also described. Methods of inhibiting neuraminidase in samples suspected of containing neuraminidase are also described. Antigenic materials, polymers, antibodies, conjugates of the compounds of the invention with labels, and assay methods for detecting neuraminidase activity are also described.

专利号:US-3753970-A
优先权日:1970-08-04
标题:Cyclopeptides derived from polymyxins and their preparation
发明人:BOUCHAUDON J; JOLLES G
权利人:RHONE POULENC SA
摘要:THE NEW CYCLOPEPTIDES OF THE FORMULA: DAB<(-DAB(-G)-Y-Z-DAB(-G)-DAB(-G)-THR-) IN WHICH Y-Z REPRESENTS AN AMINO ACID CHAIN SELECTED FROM D-LEU-THR,D-PHE-LEU, D-LEU-LEU AND D-LEU-ILEU, G REPRESENTS AN AMINO-PROTECTING RADICAL OF THE FORMULA: PY-CH(-R)-OOC- IN WHICH PY REPRESENTS PYRIDYL, PYRIDYL-N-OXIDE, OR PYRIDYL OR PYRIDYL-N-OXIDE CARRYING A METHYL SUBSTITUENT, R REPRESENTS HYDROGEN, ALKYL OF 1 TO THROUGH 5 CARBON ATOMS, OR PHENYL, AND DAB REPRESENTS A,Y-DIAMINOBUTYRIC AID, THE AMINO ACIDS HAVING THE L-CONFFIGURATION UNLESS OTHERWISE INDICATED, SAID CYCLOPEPTIDES CONTAINING ONLY A SINGLE FREE AMINO GROUP, ARE USEFUL INTERMEDIATES FOR THE SYNTHESIS OF SEMI-SYNTHETIC PRODUCTS DERIVED FROM POLYMYXINS.

供应商参考报价(招募中)

品牌试剂参考报价(招募中)

📌 第三方产品分析报告

✅ COA系统入驻 | 共享模式

主要参考文献


1: Khomenko T, Deng X, Ahluwalia A, Tarnawski A, Patel KN, Sandor Z, Szabo S. STAT3 and importins are novel mediators of early molecular and cellular responses in experimental duodenal ulceration. Dig Dis Sci. 2014 Feb;59(2):297-306. doi: 10.1007/s10620-013-2807-6. Epub 2014 Jan 3. Review. doi: 10.1073/pnas.1113081108. Epub 2011 Nov 14.
4: Takara K, Hayashi R, Kokufu M, Yamamoto K, Kitada N, Ohnishi N, Yokoyama T. Effects of nonsteroidal anti-inflammatory drugs on the expression and function of P-glycoprotein/MDR1 in Caco-2 cells. Drug Chem Toxicol. 2009;32(4):332-7. doi: 10.1080/01480540903130658. Epub 2008 Feb 9. Inorg Chem. 2003 Dec 15;42(25):8328-36.

合成参考文献


摘要:Jiao, N.; Li, Z., Science of Synthesis: Catalytic Oxidation in Organic Synthesis, (2017) 1, 703.
摘要:Schafer, E. W., Jr., and W. A. Bowles Jr. 1985. Acute oral toxicity and repellency of 933 chemicals to house and deer mice. Archives of Environmental Contamination and Toxicology 14:111-129.
摘要:Schafer, E. W., Jr., and W. A. Bowles Jr. 2004. Toxicity, Repellency of Phytotoxicity of 979 Chemicals to Birds, Mammals and Plants. Research Report No. 04-01. National Wildlife Research Center, Fort Collins, Colorado. 118 pp. https://www.aphis.usda.gov/ws/nwrc/chem-effects-db/U_schafer041_2004.pdf
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