CAS: 1073-62-7; Benzylhydrazine Hydrochloride

该化合物是一种有机化合物,其特征是附于苯基甲基(苯基)的氢锌功能组,其特征是存在一种有机化合物,它看起来像一种白色的脱白晶体,在水和酒精中可溶解,可以用于有机合成和药物的各种用途;由于氢子组可参与核分裂医学反应,因而具有基本特性;它经常用于各种氢化衍生物的合成,并作为有机化学的试剂;然而,必须谨慎地处理这种物质,因为众所周知,氢子具有毒性和潜在致癌性;在与该化合物合作时,应观察适当的安全措施,包括使用个人防护设备;此外,其盐分形式可提高其稳定性和溶性,使之适合于各种化学反应和在研究和工业中的应用.

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20570-96-1 21075-83-2 2644-70-4

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N'-benzylhydrazinecarboxylic acid tert-butyl ester benzaldehyde benzylhydrazone tert-butyl 1-benzylhydrazine-1-carboxylate N-benzyl-N'-[(tert-butoxy)carbonyl](tert-butoxy)carbohydrazide1-benzyl-3,5-dimethyl-1H-pyrazole 2-benzylthiosemicarbazide 2-benzyl thiosemicarbazideN2-benzyl thiosemicarbazide 1-Ethansulfonyl-1-benzyl-2-benzyliden-hydrazin

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    专利信息


    专利号:US-7244753-B2
    优先权日:2002-07-29
    标 题:Cyclooxygenase-2 selective inhibitors, compositions and methods of use
    发明人:GARVEY DAVID S; KHANAPURE SUBHASH P; RANATUNGE RAMANI R; RICHARDSON STEWART K; SCHROEDER JOSEPH D
    权利人:NITROMED INC
    摘要:The invention describes novel cyclooxygenase 2 (COX-2) selective inhibitors and novel compositions comprising at least one cyclooxygenase 2 (COX-2) selective inhibitor, and, optionally, at least one compound that donates, transfers or releases nitric oxide, stimulates endogenous synthesis of nitric oxide, elevates endogenous levels of endothelium-derived relaxing factor or is a substrate for nitric oxide synthase, and/or at least one therapeutic agent. The invention also provides novel kits comprising at least one COX-2 selective inhibitor, optionally nitrosated and/or nitrosylated, and, optionally, at least one nitric oxide donor, and/or, optionally, at least one therapeutic agent. The novel cyclooxygenase 2 selective inhibitors of the invention can be optionally nitrosated and/or nitrosylated. The invention also provides methods for treating inflammation, pain and fever; for treating and/or improving the gastrointestinal properties of COX-2 selective inhibitors; for facilitating wound healing; for treating and/or preventing renal and/or respiratory toxicity; for treating and/or preventing other disorders resulting from elevated levels of cyclooxygenase-2; and for improving the cardiovascular profile of COX-2 selective inhibitors.

    专利号:US-10329264-B2
    优先权日:2015-07-31
    标题 :Process for the preparation of isocarboxazid
    发明人:DE FAVERI CARLA; HUBER FLORIAN ANTON MARTIN; ANTOLINI NICOLA
    权利人:LUNDBECK PHARMACEUTICALS ITALY S P A
    摘要:This invention relates to a novel chemical process for the synthesis of N′-benzyl-5-methylisoxazole-3-carbohydrazide (Isocarboxazid) which comprises reacting 5-methyl-3-isoxazole carboxylic acid ester with benzylhydrazine or a salt thereof in an aprotic organic solvent and in the presence of an organic base.

    专利号:US-6297194-B1
    优先权日:1999-02-02
    标 题 :Production of phosphonopyrazoles
    发明人:MILLER PAULA C; CURTIS JANE M; MOLYNEAUX JOHN M; OWEN THOMAS J
    权利人:MONSANTO TECHNOLOGY LLC
    摘要:Pyrazole compounds with activity as chemical hybridizing agents and methods for synthesis of such compounds are disclosed. These compounds are useful in producing hybrid wheat (Triticum aesativum) and other crops.

    专利号:US-2002107401-A1
    优先权日:2000-02-02
    标题:Production of phosphonopyrazoles
    发明人:MILLER PAULA C; CURTIS JANE M; MOLYNEAUX JOHN M; OWEN THOMAS J
    权利人:MONSNTO TECHNOLOGY LLC
    摘要:Novel compounds with activity as chemical hybridizing agents and methods for synthesis of such compounds are disclosed. These compounds are useful in producing hybrid wheat ( Triticum aesativum ) and other crops.

    专利号:US-10226449-B2
    优先权日:2013-12-20
    标 题:Heterocyclic modulators of lipid synthesis and combinations thereof
    发明人:HEUER TIMOTHY SEAN; OSLOB JOHAN D; MCDOWELL ROBERT S; JOHNSON RUSSELL; YANG HANBIAO; EVANCHIK MARC; ZAHARIA CRISTIANA A; CAI HAIYING; HU LILY W; DUKE GREGORY; OHOL-GUPTA YAMINI; O'FARRELL MARIE
    权利人:3 V BIOSCIENCES INC
    摘要:Heterocyclic modulators of lipid synthesis are provided as well as pharmaceutically acceptable salts thereof; pharmaceutical compositions comprising such compounds; and methods of treating conditions characterized by dysregulation of a fatty acid synthase pathway by the administration of such compounds and combinations of such compounds and other therapeutic agents.

    专利号:US-9428502-B2
    优先权日:2012-07-03
    标题:Heterocyclic modulators of lipid synthesis
    发明人:OSLOB JOHAN D; MCDOWELL ROBERT S; JOHNSON RUSSELL; YANG HANBIAO; EVANCHIK MARC; ZAHARIA CRISTIANA A; CAI HAIYING; HU LILY W; WAGMAN ALLAN S
    权利人:3-V BIOSCIENCES INC
    摘要:Heterocyclic modulators of lipid synthesis are provided as well as pharmaceutically acceptable salts thereof; pharmaceutical compositions comprising such compounds; and methods of treating conditions characterized by disregulation of a fatty acid synthase pathway by the administration of such compounds.

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    📌 第三方产品分析报告

    ✅ COA系统入驻 | 共享模式

    合成参考文献


    摘要:Götzinger, A. C.; Müller, T. J. J., Science of Synthesis Knowledge Updates, (2017) 3, 130.
    摘要:Götzinger, A. C.; Müller, T. J. J., Science of Synthesis Knowledge Updates, (2017) 3, 31.
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