CAS: 3788-32-7; 2-Methylpropylcyclopentane

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CAS号53098-47-8 1-(2-methylprop...

合成工艺路线路线简述

    📜Alkaline Earth Salt Of/the/ Methylsulfuric Acid置于nickel Kieselguhr体系中,化学反应生成异丁基环戊烷
    参考文献:The Preparation Of Cyclopentenes And Cyclopentanes. I1
    标题:The Preparation Of Cyclopentenes And Cyclopentanes. I1
    摘要:
    Doi:10.1021/ja01224A002

    专利信息


    专利号:US-11130764-B2
    优先权日:2017-02-17
    标题 :Analogs of vincamine and uses thereof
    发明人:HUIGENS III ROBERT WILLIAM; NORWOOD IV VERRILL M; LUESCH HENDRIK
    权利人:UNIV FLORIDA
    摘要:The present disclosure provides compounds of any one of Formulae (I′), (I), (IA), (II′), (II), (IIA), (IIIA), (III″), (III′), (III), (IIIA), (IV), (V′), (V), (VI), (VII), (VIII′), (VIII), (IX′), (IX), and (X). The compounds described herein may be useful in treating and/or preventing a broad range of diseases (e.g., proliferative disease (e.g., cancers (e.g., non-small cell lung cancer, or glioma), inflammatory diseases, autoimmune diseases), CNS disorder (e.g., drug addiction), metabolic disorder (e.g., diabetes), or infectious disease (e.g., bacterial infection or parasitic infection (e.g., malaria))). Also provided in the present disclosure are pharmaceutical compositions, methods of synthesis of a compound described herein, kits, methods, and uses including or using a compound described herein.

    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-2010056779-A1
    优先权日:2006-09-12
    标题:Synthesis of methyl nonactate derivatives

    专利号:CN-1620295-A
    优先权日:2001-12-14
    标 题 :Preparation of intermediates useful in the synthesis of antiviral nucleosides

    专利号:US-7854934-B2
    优先权日:1999-08-20
    标 题 :Glycoconjugates, glycoamino acids, intermediates thereto, and uses thereof
    发明人:DANISHEFSKY SAMUEL J; COLTART DON M; KEDING STACY J; BISWAS KAUSTAV; LIVINGSTON PHILIP O; RAGUPATHI GOVINDASWAMI; ALLEN JENNIFER R; WILLIAMS LAWRENCE
    权利人:SLOAN KETTERING INST CANCER
    摘要:The present invention provides novel glycosides and glycoconjugates, glycoamino acids, and methods for the synthesis thereof. In another aspect, the present invention provides novel clustered glycopeptides and methods for the synthesis thereof. In still another aspect, the present invention provides methods for the treatment of cancer, preferably for the prevention of recurrence of cancer, and methods for inducing antibodies in a subject, comprising administering to a subject in need, an effective amount of any of the inventive glycopeptides as disclosed herein, either in conjugated form or unconjugated and in combination with a suitable immunogenic carrier.

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    📌 第三方产品分析报告

    ✅ COA系统入驻 | 共享模式

    主要参考文献

    参考标题:Synthesis Of Mesoporous Zsm-5 Zeolites And Catalytic Cracking Of Ethanol And Oleic Acid Into Light Olefins
    作者:Tingting Zhao,Fuwei Li,Hongchang Yu,Shilei Ding,Zhixia Li,Xinyuan Huang,Xiang Li,Xiaohan Wei,Zhenlin Wang,Hongfei Lin |发布日期:2019.4
    摘要:Selectivity (42.3%) At 400 °C. In Oleic Acid To Light Olefin Reaction, Mzsm-5-B Achieved A Complete Conversion Of Oleic Acid At 500 °C, And Obtained The Highest Light Olefin Selectivity (38.1%) At 550 °C. The Difference May Be Relevant To The Size And Chemical Structure Of Feedstock Molecular As Well As The Acidity Of Catalysts. Regardless Of Ethanol Or Oleic Acid As Feedstock, Introduction Of Mesopore

    合成参考文献


    参考文献:10.1055/s-0040-1707950
    摘要:Preparation of 3-Alkoxyquinoxalin-2-ones by Electrooxidative C–H/O–H Cross-Coupling. Synfacts. 2020 May 15;16(06):0695. doi: 10.1055/s-0040-1707950.
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