CAS: 85279-30-7; 2-Acetyl-3-Methylpyridine

该化合物是一种有机化合物,其特征是其丙烯基环结构,具有芳香特性.乙酮功能组的存在表明,它是一种酮,具体具有与乙基组相邻的碳基组(C=O)特征.由于碳基的功能性会影响其溶解于各种溶剂,这种化合物通常具有极性.其分子结构允许与生物系统发生潜在互动,使其对药用化学和药理具有兴趣.该化合物还可能表现出中度的挥发性,并能够参与各种化学反应,例如核糖基化合物添加,因为碳基碳的具有电子生物特性.此外,其独特的结构特征在某些条件下可能会产生特定的再活动模式和稳定性.应当参考安全数据,以便处理和使用,与任何化学物质一样,确保采取适当的防范措施.

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相似化合物

1344938-60-8 780804-99-1 1344930-80-8

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CAS号1603-40-3 2-氨基-3-甲基吡啶 | CAS号3430-17-9 2-溴-3-甲基吡啶 | CAS号20970-75-6 2-氰基-3-甲基吡啶 | CAS号74-88-4 碘甲烷 | CAS号832692-80-5 5-chloro-2-(3-m...

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  • 20970-75-6 + 917-64-6 = 85279-30-7
    反应条件:1.1 Reagents: Hydrochloric Acid
    标题:Compounds With Bridgehead Nitrogen. 45. The Proton Nmr Spectra And Stereochemistry Of Some Dimethylperhydrooxazolo[3,4-A]Pyridines
    作者:Crabb,Trevor A.; Heywood,Geoffrey C.
    参考文献:Organic Magnetic Resonance 日期:1982 卷标:20(4) 页码:242-8]

    20970-75-6 = 85279-30-7
    反应条件:1.1 Solvents: Diethyl Ether,Tetrahydrofuran; -20 °C; 1 - 3 H,-20 - -10 °C; -10 °C -> -40 °C1.2 Reagents: Hydrochloric Acid Solvents: Water; 5 Min,-40 °C
    标题:Effects Of Structural Modifications On The Metal Binding,Anti-Amyloid Activity,And Cholinesterase Inhibitory Activity Of Chalcones
    作者:Fosso,Marina Y.; Levine,Harry Iii; Green,Keith D.; Tsodikov,Oleg V.; Garneau-Tsodikova,Sylvie
    参考文献:Organic & Biomolecular Chemistry 日期:2015 卷标:13(36) 页码:9418-9426]

    3430-17-9 + 127-19-5 = 85279-30-7
    反应条件:1.1 Reagents: Butyllithium Solvents: Diethyl Ether,Hexane; 30 Min,-78 °C1.2 -78 °C; 1 H,-78 °C -> Rt1.3 Reagents: Ammonium Chloride Solvents: Water
    标题:Turning Cucurbit[8]Uril Into A Supramolecular Nanoreactor For Asymmetric Catalysis
    作者:Zheng,Lifei; Sonzini,Silvia; Ambarwati,Masyitha; Rosta,Edina; Scherman,Oren A.; Et Al
    参考文献:Angewandte Chemie 日期:2015 卷标:54(44) 页码:13007-13011
📜2-氨基-3-甲基吡啶置于氢溴酸,溴,碘,Magnesium,Sodium Nitrite体系中,化学反应 5.0H,反应生成 2-乙酰基-3-甲基吡啶
参考文献:Compounds With Bridgehead Nitrogen: 45-the1H NMR Spectra And Stereochemistry Of Some Dimethylperhydro-Oxazolo[3,4-A]Pyridines
标题:Compounds With Bridgehead Nitrogen: 45-the1H NMR Spectra And Stereochemistry Of Some Dimethylperhydro-Oxazolo[3,4-A]Pyridines
摘要:Abstractthe Positions Of Conformational Equilibria In 1,5‐,1‐6‐ And 1,8‐dimethylperhydro‐oxazolo[3,4‐a]Pyridines Were Determined By 1H NMR Spectroscopy. The Cis‐(H‐5,H‐8A)‐1,6‐dimethyl‐perhydro‐oxazolo[3,4‐a]Pyridine. In Contrast,R‐1,T‐6,T‐8A‐1,6‐dimethylperhydro‐oxazolo[3,4‐ A]Pyridine Preferred The Cis‐fused Conformation. Three Of The 1,8‐dimethylperhydro‐oxazolo[3,4‐a]Pyridines Adopted The Trans‐fused Conformations (With Distortion Of The System In The Case Of The R‐1,C‐8,C‐8A Derivative) And The R‐1,C‐8,T‐8A‐1,8‐dimethyl Derivative Adopted The Cis‐fused Conformation.
DOI:10.1002/mrc.1270200411

海关参考信息

专利信息


专利号:US-6608202-B1
优先权日:2001-08-21
标题:Process of synthesis of a tricyclic ketone intermediate
发明人:DORAN HENRY J; O'NEILL PAT M; WILLIAMS ROBERT P
权利人:SCHERING CORP
摘要:In one embodiment, the present invention describes the synthesis of a compound of Formula III, wherein X is halogen,and intermediates therefor from easily available starting materials by a simple route.

专利号:US-2003144314-A1
优先权日:2001-08-21
标 题 :Process of synthesis of a tricyclic ketone intermediate

专利号:US-2003050319-A1
优先权日:2000-04-18
标题:Synthesis of intermediates useful in preparing tricyclic compounds

专利号:US-6492519-B2
优先权日:2000-04-18
标题 :Synthesis of intermediates useful in preparing tricyclic compounds

专利号:US-6750347-B2
优先权日:2000-04-18
标题:Synthesis of intermediates useful in preparing tricyclic compounds
发明人:POIRIER MARC; WONG YEE-SHING; WU GEORGE G
权利人:SCHERING CORP
摘要:A process is provided for preparing a compound having the formula n wherein R is H or Cl. n Also provided is a process for preparing a compound having the formula

专利号:US-2002035261-A1
优先权日:2000-04-18
标题:Synthesis of intermediates useful in preparing tricyclic compounds

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✅ COA系统入驻 | 共享模式

合成参考文献


参考文献:10.1055/s-0041-1737139
摘要:Tran AT, Tran CV, Le HV, Tran LV, Tran TTP, Tran SV. Design, Synthesis, and Cytotoxic Activity of New Tubulysin Analogues. Synlett. 2021 Nov 19;33(02):187–95. doi: 10.1055/s-0041-1737139.
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