CAS: 1613-37-2; Quinoline 1-Oxide

该化合物是一种有机化合物,其结构特征是其结构,由带有N-氧化功能组的quinoline环组成;通常是在水和酒精等极溶剂中溶解的黄色至褐色的灰色固体;该化合物以其作为有机合成中间体和各种化学反应的试剂的作用而著称,特别是在医药化学领域;N-氧化氮展示其特性,如其基质薄弱,并能够参与因N-氧化物组的存在而引发的再氧化反应;它也因其潜在的生物活动而得到承认,包括抗微生物和抗脉冲特性;然而,处理该化合物需要谨慎,因为它可能构成健康风险,包括对皮肤和呼吸系统造成刺激;与许多化学物质一样,在与N-氧化氮基线合作减少任何潜在危害时,应当遵循适当的安全议定书.

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

quinoline Perbenzoic acid benzene trifluoroacetyl peroxide2-hydroxyquinoline quinoline-2-carbonitrile 3-nitroquinoline N-oxide H-quinolin-2-one1-benzoyloxy-3,6-dinitro-1H-quinolin-2-one

合成工艺路线路线简述

    喹啉置于phosphomolybdic Acid,双氧水体系中,用 乙醇,水,乙腈 用作溶剂,化学反应 12.0H,以88%的收率获得喹啉-N-氧化物
    参考文献:Synthetic And Mechanistic Aspects Of The Regioselective Base-Mediated Reaction Of Perfluoroalkyl-And Perfluoroarylsilanes With Heterocyclic N-Oxides
    标题:Synthetic And Mechanistic Aspects Of The Regioselective Base-Mediated Reaction Of Perfluoroalkyl-And Perfluoroarylsilanes With Heterocyclic N-Oxides
    摘要:已开发出一种新颖高效的直接全氟烷基化嗪n-氧化物的方法,并提供了有趣的机理细节.
    Doi:10.1039/c4Ob01088D

    海关参考信息

    专利信息


    专利号:US-12421534-B2
    优先权日:2021-11-10
    标 题 :Engineered enzymes and method for the synthesis of diverse tyrosine analogs
    发明人:ALMHJELL PATRICK J; ARNOLD FRANCES H
    权利人:CALIFORNIA INST OF TECHN
    摘要:Provided herein is an engineered tryptophan synthase β-subunit (TrpB) that catalyzes the synthesis of tyrosine, tyrosine analogs, or salts thereof. Also provided herein are methods for preparing tyrosine, tyrosine analogs, or a salt thereof using the engineered TrpB described herein.

    专利号:WO-2013138200-A1
    优先权日:2012-03-13
    标 题 :Green chemistry synthesis of the malaria drug amodiaquine and analogs thereof
    发明人:FORTUNAK JOSEPH MARIAN; KULKARNI AMOL ANANT; KING CHRISTOPHER
    权利人:UNIV HOWARD
    摘要:Methods are provided for a green chemistry one-pot synthesis of amodiaquine and amodiaquine analogs. The methods have a lower environmental impact, lower investment cost, reduced amounts of byproducts and impurities, and a shorter synthesis time, compared to current conventional synthesis methods. The methods reduce the total number of steps in the synthesis from four to five down to two, thereby simplifying production; and allow a reduced number of solvents and reagents to be used in production, thereby reducing the waste generated in the synthesis. The methods can reduce the waste to about 3-5 kilograms of waste generated per kilogram of product produced; and surprisingly improve the overall yield from 60-65% to greater than 90% as compared to the current conventional synthesis methods for amodiaquine and its analogs.

    专利号:US-5521310-A
    优先权日:1992-10-07
    标 题 :Process to obtain benzoxazines to be used for the synthesis of ofloxazine, levofloxazine and derivatives
    发明人:CARRETERO GONZALVEZ JUAN-CARLO; VICIOSO SANCHEZ MERCEDES; GARCIA RUANO JOSE-LUIS
    权利人:ETILO DERIVADOS
    摘要:A process to obtain benzoxazines useful for the synthesis of Ofloxazine, Levofloxazine and derivatives. The benzoxacines (I) where Xb is an halogen and R 1 is H, alkyl or alkenyl of up to 6 atoms of C or aryl, can be obtained by means of cycling a compound of formula (II) through the reaction with triphenylphosphine and ethyl azodicarboxilate. The compounds of formula (II) can be obtained through the reaction of a compound (III) with an adequate epoxide. Through the use of the adequate chiral epoxide it is possible to obtain the enantiomerically desired intermediate and, therefore and selectively, it is possible to obtain the desired final product with the adequate enantiomeric form without the need to carry out a resolution stage. n The Compounds (I) are useful and key intermediates for the synthesis of the antimicrobials Oflixazine and Levofloxazine. ##STR1##

    专利号:US-2003182068-A1
    优先权日:2001-10-30
    标 题 :Device and methods for directed synthesis of chemical libraries
    发明人:BATTERSBY BRONWYN J; MILLER CHRISTOPHER R; TRAU MATHIAS; WAY JEFFERY C; JOHNSTON ANGUS
    摘要:The invention features a sort computer which interfaces with a sorting device in order to control the sorting of beads on a bead by bead basis. The invention further features novel methods for the directed synthesis of encoded libraries of oligomers, e.g., oligonucleotides, on beads. These methods allow the synthesis of libraries that are sufficiently large to permit complex genomic analyses to be carried out. New methods of using the encoded libraries also are described.

    专利号:US-10768157-B2
    优先权日:2015-10-20
    标 题:Materials and methods for the detection of trace amounts of substances in biological and environmental samples
    发明人:KABIR ABUZAR; FURTON KENNETH G
    权利人:KABIR ABUZAR; FURTON KENNETH G; THE FLORIDA INTERNATIONAL UNIV BOARD OF TRUSTEES
    摘要:The subject invention provides chemical compositions and synthesis strategies to create molecularly imprinted polymers (MIPs) via sol-gel processes. In a specific embodiment, the subject invention utilizes a(n) organic, inorganic, or metallic template analyte to create a hybrid organic-inorganic or inorganic three-dimensional network possessing cavities complementary to the shape, size, and functional orientation of the template molecule or ions. The subject invention further pertains to the use of the novel MIPs as selective solid phase extraction (SPE) sorbents for pre-concentration and clean-up of trace substances in biological and environmental samples. Synthesis of other molecularly imprinted polymers with environmental, pharmaceutical, chemical, clinical, toxicological, and national security implications can be conducted in accordance with the teachings of the subject invention.

    专利号:WO-2015198349-A1
    优先权日:2014-06-25
    标 题 :A one pot synthesis of 3-substituted quinoline carboxylates and its derivatives
    发明人:GADAKH SUNITA KHANDERAO; SUDALAI ARUMUGAM
    权利人:COUNCIL SCIENT IND RES
    摘要:The present invention provides a one pot, simple, cost effective and industrially feasible catalytic synthesis of quinolines or substituted quinolines from anilines with yield >80% yield. The present invention also discloses a process for the synthesis of oxolinic acid using quinolines with yield > 45%.
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    合成参考文献


    摘要:Joule, J. A., Science of Synthesis Knowledge Updates, (2010) 2, 258.
    摘要:Silva, V. L. M.; Pinto, D. C. G. A.; Santos, C. M. M.; Rocha, D. H. A., Science of Synthesis Knowledge Updates, (2022) 3, 419.
    摘要:Ye, Z.-S., Science of Synthesis Knowledge Updates, (2021) 2, 410.
    摘要:Yeung, C. S.; Borduas, N.; Dong, V. M., Science of Synthesis: Cross Coupling and Heck-Type Reactions, (2012) 3, 791.
    摘要:Nakao, Y., Science of Synthesis: Catalytic Transformations via CH Activation, (2015) 1, 343.
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