CAS: 85-90-5; 3-Methylchromone

该化合物是一种甲基替代苯丙丙酮衍生物,可能用于有机合成和制药研究,其结构框架以结合苯和皮兰环系统为特点,使其成为开发生物活性化合物的宝贵中间体. 3级的甲基组在各种化学转化中增强了反应性和选择性.该化合物的特点是稳定性和纯度,确保合成工作流程的一贯性能.其定义明确的分子结构允许精确的修改,使之适合用于医药化学和材料科学.在高纯度等级中,它符合严格的研究和工业要求.

结构式图片

欧盟法规

ECHA物质C&L通报REACH预注册

上下游产品

色酮-3-甲醛 3-Formylchromone 17422-74-1
3-Methyl-2-Methylsulfanylchromen-4-One 868732-17-6
3-Methyl-4-Oxo-4H-Chromene-2-Carboxylic Acid 104094-15-7

合成工艺路线路线简述

    3-(2-Bromophenyl)-2-Methyl-3-Oxopropanal置于2-吡啶甲酸,Copper(L) Iodide,Potassium Carbonate体系中,用 N,N-二甲基甲酰胺 作为反应溶剂,化学反应 20.0H,以64%的收率获得产物甲色酮
    参考文献:铜(i)催化的分子内环化反应合成异黄酮
    标题:铜(i)催化的分子内环化反应合成异黄酮
    摘要:异黄酮衍生物是通过以cui为催化剂,以2-吡啶甲酸(=吡啶-2-羧酸)为配体,以k 2 Co 3为催化剂,通过3-(2-溴苯基)-3-氧丙醛衍生物的分子内环化反应合成的.碱和dmf作作为反应溶剂,产率高达96%.合成是官能团耐受的.
    DOI:10.1002/hlca.201000400

    海关参考信息

    专利信息


    专利号:US-10925977-B2
    优先权日:2006-10-05
    标 题 :Efficient synthesis of chelators for nuclear imaging and radiotherapy: compositions and applications
    发明人:YANG DAVID J; YU DONGFANG; THOMPSON ANDREW S
    权利人:YANG DAVID J; YU DONGFANG; THOMPSON ANDREW S; CEIL POINT LLC; UNIV TEXAS
    摘要:Novel methods of synthesis of chelator-targeting ligand conjugates, compositions comprising such conjugates, and therapeutic and diagnostic applications of such conjugates are disclosed. The compositions include chelator-targeting ligand conjugates optionally chelated to one or more metal ions. Methods of synthesizing these compositions in high purity are also presented. Also disclosed are methods of imaging, treating and diagnosing disease in a subject using these novel compositions, such as methods of imaging a tumor within a subject and methods of diagnosing myocardial ischemia.

    专利号:US-6951878-B2
    优先权日:1998-03-12
    标 题:Benzo[b]thiophenyl or tetrahydro-benzo[b]thiophenyl modulators of protein tyrosine phosphatases (PTPases)
    发明人:MOELLER NIELS PETER HUNDAHL; ANDERSEN HENRIK SUNE; IVERSEN LARS FOGH; OLSEN OLE HVILSTED; BRANNER SVEN; HOLSWORTH DANIEL DALE; BAKIR FARID; JUDGE LUKE MILBURN; AXE FRANK URBAN; JONES TODD KEVIN; RIPKA WILLIAM CHARLES; GE YU; UYEDA ROY TERUYUKI
    权利人:NOVO NORDISK AS
    摘要:The present invention provides novel compounds, novel compositions, methods of their use, and methods of their manufacture, where such compounds are pharmacologically useful inhibitors of Protein Tyrosine Phosphatases (PTPase's) such as PTP1B, CD45, SHP-1, SHP-2, PTPα, LAR and HePTP or the like. n The compounds are useful in the treatment of type I diabetes, type II diabetes, impaired glucose tolerance, insulin resistance, obesity, immune dysfunctions including autoimmunity diseases with dysfunctions of the coagulation system, allergic diseases including asthma, osteoporosis, proliferative disorders including cancer and psoriasis, diseases with decreased or increased synthesis or effects of growth hormone, diseases with decreased or increased synthesis of hormones or cytokines that regulate the release of/or response to growth hormone, diseases of the brain including Alzheimer's disease and schizophrenia, and infectious diseases.

    专利号:US-7666890-B2
    优先权日:2006-06-13
    标题 :Synthesis and herbicidal activity of 1- (2-substituted benzo[d]thiazol-5-yl)-1H-1,2,4-triazol-5(4H)- one derivatives
    发明人:YANG GUANGFU; LUO YANPING; LIU ZUMING
    权利人:UNIV HUAZHONG NORMAL
    摘要:Synthesis and herbicidal activity of novel 1-(2-substituted benzo[d]thiazol-5-yl)-1H-1,2,4-triazol-5(4H)-one derivatives. Using a dose of 300 gai./h, the compounds of the invention possess significant herbicidal activity for Echinochloa crusgalli, Digiatria sanguinalis, Setaria viridis, Brassica juncea, Amaranthus retroflexus and Chenopodium album.

    专利号:US-7186709-B2
    优先权日:2002-08-27
    标 题:Dihydropyrancarboxamides and uses thereof
    发明人:SCHREIBER STUART L; STAVENGER ROBERT A; MITCHISON TIMOTHY J; MALIGA ZOLTAN
    权利人:HARVARD COLLEGE
    摘要:The present invention provides novel dihydropyrancarboxamide compounds of formula (I): n nand collections of these compounds, and provides methods for the synthesis of these compounds; wherein R 1 –R 6 are as defined herein. Additionally, the present invention provides pharmaceutical compositions and methods for treating disorders such as proliferative diseases, and cancer, to name a few.

    专利号:US-10814013-B2
    优先权日:2006-10-05
    标 题 :Efficient synthesis of chelators for nuclear imaging and radiotherapy: compositions and applications

    专利号:AU-2007308022-A2
    优先权日:2006-10-05
    标题 :Efficient synthesis of chelators for nuclear imaging and radiotherapy: compositions and applications
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    主要参考文献

    [参考文献]: De Carolis D. Trattamento E Prevenzione Delle Crisi Anginose Di Origine Coronarica Con Il Metil-3-Cromone (M-3C) [参考文献]: G Clin Med. 1957;38(8):1158-1179.

    合成参考文献


    摘要:Makida, Y.; Kuwano, R., Science of Synthesis: N-Heterocyclic Carbenes in Catalytic Organic Synthesis, (2016) 1, 273.
    摘要:Farmaco, Edizione Scientifica., 13(619), 1958
    参考文献:10.1107/s1600536810020453
    摘要:Hao L, Chen J, Zhang X. 3-Methyl-4H-chromen-4-one. Acta Crystallogr Sect E Struct Rep Online. 2010 Jun 05;66(Pt 7):o1564.
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