CAS: 44565-47-1; N-Methyl-2-(Methylamino)Acetamide

该化合物是具有氨化功能组特征的有机化合物,其特征是附于该矿氮原子的甲基组,有助于其甲基氨基结构.该化合物一般无色可粉黄黄色液体或固态,取决于其纯度和温度.该化合物在水和各种有机溶剂中可溶解,可适用于不同的化学用途.N-Meby-2-(甲基氨基)乙酰胺经常用于合成制药和农用化学品,因为它能够作为有机合成的建筑块.甲基和矿类组的存在都增强了其再活动性,使其能够参与各种化学反应,包括核分裂替代和凝聚反应.安全数据表明,与许多氨化物一样,应谨慎地处理该物质,因为如果被吸收或吸入,可能会对健康造成危害.在实验室环境中与该化合物打交道时,应当遵循适当的安全议定书.

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CAS号79-04-9 氯乙酰氯 | CAS号74-89-5 氨基甲烷 | CAS号52605-49-9 肌氨酸乙酯盐酸盐 | CAS号105-39-5 氯乙酸乙酯 | CAS号13515-93-0 肌氨酸甲酯盐酸盐 | CAS号64-17-5 乙醇

合成工艺路线路线简述

    📜2-氯-N-甲基乙酰胺,甲胺 以 四氢呋喃 作为反应溶剂,化学反应 24.0H,反应生成 N~1~,N~2~-二甲基甘氨酸酰胺
    参考文献:The Structure-Activity Profile Of Mercaptobenzamides' Anti-Hiv Activity Suggests That Thermodynamics Of Metabolism Is More Important Than Binding Affinity To The Target
    标题:The Structure-Activity Profile Of Mercaptobenzamides' Anti-Hiv Activity Suggests That Thermodynamics Of Metabolism Is More Important Than Binding Affinity To The Target
    摘要:Mercaptobenzamide Thioesters And Thioethers Are Chemically Simple Hiv-1 Maturation Inhibitors With A Unique Mechanism Of Action,Low Toxicity,And A High Barrier To Viral Resistance. A Structure-Activity Relationship (Sar) Profile Based On 39 Mercaptobenzamide Prodrug Analogs Exposed Divergent Activity/toxicity Roles For The Internal And Terminal Amides. To Probe The Relationship Between Antiviral Activity And Toxicity,We Generated An Improved Computational Model For The Binding Of Mercaptobenzamide Thioesters (Samts) To The Hiv-1 Ncp7 C-Terminal Zinc Finger,Revealing The Presence Of A Second Low-Energy Binding Orientation,Hitherto Undisclosed. Finally,Using NMR-Derived Thiol-Thioester Exchange Equilibrium Constants,We Propose That Thermodynamics Plays A Role In Determining The Antiviral Activity Observed In The Sar Profile. (C) 2019 Published By Elsevier Masson Sas.
    DOI:10.1016/j.Ejmech.2019.06.020

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    专利信息


    专利号:US-11008358-B2
    优先权日:2015-03-25
    标题:Synthesis of desosamines
    发明人:MYERS ANDREW G; ZHANG ZIYANG
    权利人:HARVARD COLLEGE
    摘要:The present invention provides desosamine and mycaminose analogs and nitro sugars and methods for their preparation. The invention also provides methods of cyclizing a compound of Formula (A′) with glyoxal to give a nitro sugar of Formula (B). Methods for the preparation of compound of Formula (D′) are provided comprising cyclization of a nitro alcohol to give a nitro sugar and reduction and alkylation of the nitro sugar to give a desosamine, mycaminose, or an analog thereof.

    专利号:US-2020347087-A1
    优先权日:2015-03-25
    标题:Synthesis of desosamines

    专利号:WO-2016154533-A1
    优先权日:2015-03-25
    标 题 :Synthesis of desosamines

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    ✅ COA系统入驻 | 共享模式

    合成参考文献


    摘要:S. P. Datta, R. Leberman, and B. R. Rabin. Trans. Faraday Soc. 55, 1982 (1959).
    摘要:Simmons, N.; Chheda, P.; Schuman, D., Science of Synthesis: DNA-Encoded Libraries, (2024) nan, 404.
    摘要:Li, Y.; Fang, X.; Wang, Y., Science of Synthesis: DNA-Encoded Libraries, (2024) nan, 49.
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