CAS: 1073-21-8; 2,4-Dimethylpyridin-3-Amine

该化合物是属于含有氮的芳香热循环化合物的类的有机化合物,这种特定化合物具有氨基氨基化合物(-NH2)和附于环的两组甲基混合物(-CH3),具体地在3,2和4个位置上;它没有色素,可粉黄液或固体,视温度和纯度而定;氨基氨基化合物的存在使它成为基本化合物,能够形成酸盐;3-Amino-2,4-二甲基丙烯基苯在水和酒精等极溶剂中溶解,并具有中等的挥发性;该化合物经常用于有机合成和中间生产药品,农用化学品和其他精密化学品;该化合物还可能展示生物活动,从而引起对医药化学的兴趣;与许多含氮的热循环一样,必须谨慎处理,因为潜在的毒性和环境影响.

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1074-76-6 1193-71-1 3430-10-2

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CAS号1074-76-6 2,4-二甲基-3-硝基吡啶 | CAS号55314-30-2 2,4-二甲基烟酸 | CAS号89793-08-8 6-氯-2,4-二甲基-3-硝基吡啶 | CAS号108-47-4 2,4-二甲基吡啶 | CAS号22934-24-3 4,6-二甲基-5-硝基-2(... | CAS号897733-12-9 6-溴-2,4-二甲基吡啶-3-胺 | CAS号27296-76-0 2,4-二甲基-3-羟基吡啶

合成工艺路线路线简述

    📜2,4-二甲基吡啶置于盐酸,Palladium On Activated Charcoal,硫酸,Potassium Nitrate体系中,化学反应生成2,4-二甲基-3-氨基吡啶
    参考文献:Furukawa,Yakugaku Zasshi/journal Of The Pharmaceutical Society Of Japan,1956,Vol. 76,P. 900
    标题:Furukawa,Yakugaku Zasshi/journal Of The Pharmaceutical Society Of Japan,1956,Vol. 76,P. 900

    专利信息


    专利号:US-8742028-B2
    优先权日:2009-05-06
    标 题:Solid support for Fmoc-solid phase synthesis of peptide acids
    发明人:SRIVASTAVA KRIPA S; DAVIS MATTHEW R
    权利人:SRIVASTAVA KRIPA S; DAVIS MATTHEW R; MALLINCKRODT LLC
    摘要:The present invention provides a solid support for Fmoc-solid phase synthesis of peptides. In particular, the solid supports of the invention may be utilized to produce peptide acids.

    专利号:US-2010286359-A1
    优先权日:2009-05-06
    标题:Solid Support for FMOC-Solid Phase Synthesis of Peptide Acids

    专利号:US-6617444-B1
    优先权日:1999-06-30
    标题 :Dinucleotide tetraphosphate crystals
    发明人:MORI KENYA; MIYASHITA TAKANORI; MAEDA HIDEAKI; SATO HIROSHI; NODA YUTAKA
    权利人:YAMASA CORP
    摘要:The present invention is directed to crystals of P1-(2'-deoxycytidine 5'-)P4-(uridine 5'-)tetraphosphate (dCP4U) or a salt thereof and to a process for producing the crystals. The present invention also provides a process for producing dCP4U involving reacting uridine 5'-monophosphate (UMP), 2'-deoxycytidine 5'-monophosphate (dCMP), diphenyl phosphorochloridate (DPC), and pyrophosphate (PPi). The crystals of dCP4U obtained through the process according to the present invention have high purity and high stability and no hygroscopicity as compared with a freeze-dried product, and thereby serve as a useful raw material for preparing a pharmaceutical. The process for producing dCP4U according to the present invention permits use of inexpensive UMP as a raw material and realizes high yield. Thus, the process is suitable for large-scale synthesis of dCP4U.

    专利号:WO-2020102730-A1
    优先权日:2018-11-16
    标 题:Improved synthesis of key intermediate of kras g12c inhibitor compound

    专利号:CN-109503462-A
    优先权日:2019-01-21
    标 题:A new method for the synthesis of tofacitinib intermediate (3R,4R)-N,4-dimethyl-1-benzyl-3-piperidinamine and its oxalate hydrate

    专利号:EP-3880670-B1
    优先权日:2018-11-16
    标题 :Improved synthesis of key intermediate of kras g12c inhibitor compound

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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

    参考DOI号:10.1021/jm00098a011
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