CAS: 6084-58-8; O-Isobutylhydroxylamine Hydrochloride

该化合物是一种氢氧胺衍生物,在有机合成和制药应用中用作多种用途的中间体,其盐分盐形式增强稳定性和溶性,便利处理和储存,该化合物在氧化氮,氢氧酸和其他含氮功能组的准备方面特别宝贵,其异丁基替代成分有助于核生殖添加和凝聚反应的有利反应.该产品具有高纯度和一贯性能,适合需要精确控制反应条件的研究和工业过程.建议在无水条件下适当储存以保持其完整性.

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3332-29-4 74124-04-2 1545842-40-7

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CAS号52026-51-4 O-1-(2-methyl)p... | CAS号5618-62-2 O-异丁基羟胺

合成工艺路线路线简述

    O-异丁基羟胺置于盐酸体系中,用 乙醇 作为反应溶剂,化学反应 72.0H,反应生成 O-异丁氧基胺盐酸盐
    参考文献:Synthesis And Fungicidal Activity Of Macrolactams And Macrolactones With An Oxime Ether Side Chain
    标题:Synthesis And Fungicidal Activity Of Macrolactams And Macrolactones With An Oxime Ether Side Chain
    摘要:Three Series Of Novel Macrolactams And Macrolactones-12-Alkoxyimino-Tetradecanlactam,12-Alkoxyiminopentadecanlactam,And 12-Alkoxyiminodecanlactone Derivatives (7A,7B,And 7C)-Were Synthesized From Corresponding 12-Oxomacrolactams And 12-Oxomacrolactone. Their Structures Were Confirmed By H-1 NMR And Elemental Analysis. The Z And E Isomers Of 7A And 7B Were Separated,And Their Configurations Were Determined By H-1 NMR. These Compounds Showed Fair To Excellent Fungicidal Activities Against Rhizoctonia Solani Kuhn. It Is Interesting That The Z And E Isomers Of Most Of The Compounds Have Quite Different Fungicidal Activities. The Fact That The Compounds Have A Gradual Increase Of Fungicidal Activity In The Order Of 7A,7C,And 7B Indicated That The Macrocyclic Derivatives With A Hydrogen-Bonding Acceptor (=n-O-) And A Hydrogen-Bonding Donor (-Conh-) On The Ring,And A Three Methylenes Distance (Ch2Ch2Ch2) Between These Two Functional Groups,Exhibited The Best Fungicidal Activity. The Bioassay Also Showed That 7B Not Only Has Good Fungicidal Activity But Also May Have A Broad Spectrum Of Fungicidal Activities.
    DOI:10.1021/jf072733+

    海关参考信息

    专利信息


    专利号:US-5510511-A
    优先权日:1992-01-14
    标 题 :Process for preparing N,O-dialkylhydroxylamine, its salts or intermediates in their synthesis
    发明人:INOKI SATOSHI; TAKESUE MITSUYUKI; HASHIMOTO ISAO; KIHARA NORIAKI; SUGI KIYOAKI
    权利人:MITSUI PETROCHEMICAL IND
    摘要:A process for preparing N,O-dialkylhydroxycarbamic acid ester which comprises reacting hydroxylamine or its salt with dihydrocarbyl carbonate in the presence of a basic compound to prepare hydroxycarbamic acid ester and subsequently alkylating this compound with an alkylating agent; a process for recovering N,O-dialkylhydroxycarbamic acid ester which comprises azeotropically distilling the ester with water from a solution containing the ester; a process for preparing N,O-dialkylhydroxylamine which comprises hydrolyzing N,O-dialkylhydroxycarbamic acid ester in an aqueous solution or a hydrous solvent in the presence of an alkali; a process for purifying N,O-dialkylhydroxylamine hydrochloride which comprises adding aldehyde or ketone to a solution of N,O-dialkylhydroxylamine hydrochloride containing O-alkylhydroxylamine hydrochloride as impurities to convert the O-alkylhydroxylamine hydrochloride into O-alkyl aldoxime or O-alkyl ketoxime and subsequently separating the N,O-dialkylhydroxylamine hydrochloride from the reaction system; and a process for separating N,O-dialkylhydroxylamine hydrochloride which comprises (i) adding benzene or alkylated benzene to an aqueous solution containing N,O-dialkylhydroxylamine hydrochloride, azeotropically removing water or a hydrochloride solution, and, subsequently (ii)adding alcohol thereto to obtain N,O-dialkylhydroxylamine hydrochloride in the form of crystal.

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    合成参考文献


    参考文献:10.1038/s41419-024-06672-z
    摘要:Luo W, Zou Z, Nie Y, Luo J, Ming Z, Hu X, Luo T, Ouyang M, Liu M, Tang H, Xie Y, Peng K, Chen L, Zhou J, Luo Z. ASS1 inhibits triple-negative breast cancer by regulating PHGDH stability and de novo serine synthesis. Cell Death Dis. 2024 May 06;15(5):319.
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