CAS: 4104-45-4; 3-(Methylthio)Propylamine

该化合物是一种有机化合物,其特点是有丙基胺脊柱被甲基硫基替代,该化合物具有与一个矿类(-NH2)相连的三碳链(丙基),有助于其基本性和潜在反应性;甲基乙基胺组(-S-CH3)增强了其核分裂性,并能够影响其溶剂的溶解性,通常由于矿物质的存在而使其在极地溶剂中更易溶解. 3-(甲基乙基硫)丙基胺经常用于有机合成,并可作为生产药品,农用化学品或其他特殊化学品的中间体,其特性,如沸点,熔点和再活性,可因环境条件和其他功能组的存在而变化.在处理该化合物时,应考虑到安全因素,因为氨可能对皮肤和呼吸系统产生刺激.适当的储存和处理程序对于确保实验室或工业环境中的安全至关重要.

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2419-62-7 773803-59-1 70961-63-6

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上下游产品

-1H-isoindole-1,3(2H)-dione2-2-(Methylthio)propyl-1H-isoindole-1,3(2H)-dione 3-(methylthio)propionitrile DL-methionine L-Cysteine iberverin N-benzenesulfonyl-N'-(3-methylsulfanyl-propyl)-ureaN-benzenesulfonyl-N'-(3-methylsulfanyl-propyl)-urea N-(4-chloro-benzenesulfonyl)-N'-(3-methylsulfanyl-propyl)-ureaN-(4-chloro-benzenesulfonyl)-N'-(3-methylsulfanyl-propyl)-urea 3-aminopropranesulfonic acid

合成工艺路线路线简述

    📜L-蛋氨酸置于异佛尔酮体系中,用 异丙醇 作为反应溶剂,化学反应 4.0H,以90%的收率获得产物3-(甲基三)丙烯酸呋喃
    参考文献:氨基酸的有机催化脱羧是生物胺和酰胺的一种途径
    标题:氨基酸的有机催化脱羧是生物胺和酰胺的一种途径
    摘要:通过发酵获得或从蛋白质废水解物中回收的氨基酸代表了生产生物基化学品的极好的可再生资源.为了回收碳和氮,我们在此报告了一种化学催化,无金属的氨基酸脱羧方法,从而提供了直接接触伯胺的途径.在羰基化合物存在下,氨基酸被暂时捕获到席夫碱中,从而消除了co 2.可能会更容易进行.在评估了不同类型的醛和酮在低催化剂负载量(<=5Mol%)下的活性后,异佛尔酮在温和条件下被认为是功能强大的有机催化剂.优化后,在150oc下,在2-丙醇中,许多具有中性侧链的氨基酸以28-99%的产率转化.当反应在dmf中进行时,胺很容易发生n甲酰化.该连续反应由氨基酸反应物本身的酸度催化.通过这种方法,许多氨基酸在一锅催化系统中被有效地转化为相应的甲酰胺.
    DOI:10.1002/cctc.201900800

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    专利信息


    专利号:WO-2025069039-A1
    优先权日:2023-09-28
    标题:An in situ process for the preparation of primary amine compounds
    发明人:SAMANT RAJARAM; TONGRA MANOJ
    权利人:SAMANT RAJARAM; TONGRA MANOJ
    摘要:An in situ process for the preparation of primary amine compounds The invention disclosed herein relates to an in situ process for the preparation of primary amine compounds. Particularly, it relates to the preparation of primary amine compounds having general Formula (I). Formula (I) wherein n is 1 to 9 and X is -S, -N- or -O. More particularly, the present invention relates to the preparation of primary amine compounds with high yield and purity which is further used as potent intermediate in the synthesis of therapeutically active isothiocyanates (ITCs).

    专利号:US-4086423-A
    优先权日:1973-10-12
    标题 :Process for cephem synthesis
    发明人:FIRESTONE RAYMOND A; RATCLIFFE RONALD W; CHRISTENSEN BURTON G
    权利人:MERCK & CO INC
    摘要:Cephalosporin antibiotics of the formula: ##STR1## are produced by cycloaddition of a glycine derivative of the formula ##STR2## with a thiazine derivative of the formula ##STR3##

    专利号:US-5064962-A
    优先权日:1989-02-23
    标题:Diaminothiophenes
    发明人:WIESENFELDT MATTHIAS; ETZBACH KARL-HEINZ
    权利人:BASF AG
    摘要:Diaminothiophenes of the formula or tautomers thereof, where R1 and R2 are each hydrogen or together are where T1 is hydrogen, alkyl or phenyl, T2 and T3 are, independently of one another, alkyl or phenyl, or T2 and T3 together with the nitrogen linking them are a heterocyclic radical, R3 is substituted amino and R4 is alkanoyl, benzoyl, cyano, nitro or where T4 is hydrogen, alkyl or phenyl and T5 is the radical of a primary amine or of an active methylene compound, are prepared as described. The present diaminothiophene compound is useful in the synthesis of dyes, crop protection agents and pharmaceuticals.

    专利号:WO-2024256496-A1
    优先权日:2023-06-14
    标题 :[1,2,4]-triazolo[4,3-b]pyridazine derivatives useful as a medicament
    发明人:ELIE JONATHAN; GEORGE PASCAL; MIEGE FRÉDÉRIC; MEIJER LAURENT
    权利人:PERHA PHARMACEUTICALS
    摘要:The present invention relates to a compound of formula (I) or any of its pharmaceutically acceptable salt. The present invention further relates to a synthesis process for manufacturing compound of formula (I) or any of its pharmaceutically acceptable salts, comprising at least a step of reacting a compound of formula (II) with an amine of formula (IV) NHR5R6 for example in a molar ratio ranging from 1 to 20 eq, with respect to the compound of formula (II), in an aprotic solvent or without solvent or else in a protic solvent.

    专利号:US-2008176865-A1
    优先权日:2005-06-15
    标 题:Substituted arylpyrazoles
    发明人:BILLEN DENIS; BOYLE JESSICA; CRITCHER DOUGLAS JAMES; GETHIN DAVID MORRIS; HALL KIM THOMAS; KYNE GRAHAM MICHAEL
    权利人:PFIZER LTD
    摘要:This invention relates to a range of 1-aryl-4-cyclopropylpyrazoles in which the cyclopropyl ring is substituted at the angular position, and pharmaceutically acceptable salts and solvates thereof, to compositions comprising such compounds, processes to their synthesis and their use as parasiticides.

    专利号:US-7968584-B2
    优先权日:2005-06-15
    标 题:Substituted arylpyrazoles
    发明人:BILLEN DENIS; BOYLE JESSICA; CRITCHER DOUGLAS JAMES; GETHIN DAVID MORRIS; HALL KIM THOMAS; KYNE GRAHAM MICHAEL
    权利人:PFIZER; PFIZER PROD INC
    摘要:This invention relates to a range of 1-aryl-4-cyclopropylpyrazoles in which the cyclopropyl ring is substituted at the angular position, and pharmaceutically acceptable salts and solvates thereof, to compositions comprising such compounds, processes to their synthesis and their use as parasiticides.

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    ✅ COA系统入驻 | 共享模式

    主要参考文献

    [参考文献]: Gavin L Sacks, Et Al. High-Precision Position-Specific Isotope Analysis Of 13C/12C In Leucine And Methionine Analogues. Anal Chem. 2003 Oct 15;75(20):5495-503.
    [参考文献]: H Hibasami, Et Al. Inhibition By Polyamines Of Methylthiopropylamine-Induced Ornithine Decarboxylase In Human Lymphoid Leukemia Molt 4B Cells. Biochem Pharmacol. 1989 Nov 1;38(21):3673-6.
    [参考文献]: Ming-Fu Lin, Et Al. Photodissociation Of S Atom Containing Amino Acid Chromophores. J Chem Phys. 2007 Aug 14;127(6):064308.
    [参考文献]: Olga B Morozova, Et Al. Time-Resolved Chemically Induced Dynamic Nuclear Polarization Studies Of Structure And Reactivity Of Methionine Radical Cations In Aqueous Solution As A Function Of Ph. J Phys Chem A. 2005 Nov 17;109(45):10459-66.
    [参考文献]: Tamás Gáti, Et Al. Adducts Of Rh2[mtpa]4 With Some Phosphine Chalcogenides: Nature Of Binding And Ligand Exchange. Magn Reson Chem. 2004 Jul;42(7):600-4.

    合成参考文献


    参考文献:10.1007/s00216-011-5203-0
    摘要:Torreggiani A, Barata-Vallejo S, Chatgilialoglu C. Combined Raman and IR spectroscopic study on the radical-based modifications of methionine. Analytical and Bioanalytical Chemistry. 2011 Jul 15;401(4):1231. doi: 10.1007/s00216-011-5203-0.
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