CAS: 547-65-9; 3-Methylenedihydrofuran-2(3H)-One

该化合物是自然形成的化学化合物,被归类为精液内酯,主要来自图利帕基因的各种物种,特别是郁金香,其特点是独特的结构,包括内酯环和多种双环,有助于其反应和生物活动.图利帕林A以其潜在的医学特性而著称,包括抗炎和抗微生物效应,尽管为了充分理解其机制和应用需要进一步研究.此外,图利帕林A的研究还呈现出一种独特的气味,可归因于其不稳定性.由于它的生物活动,图利普林A在药理学和自然产品化学领域都引起了兴趣.然而,必须指出,接触图利帕林A可能会引起一些人的过敏反应,尤其是那些对郁金粉或相关化合物敏感的反应.与许多自然产品一样,图利普林A的研究继续演变,揭示了它在生态和治疗方面的重要性.

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

CAS号201230-82-2 carbon monoxide | CAS号927-74-2 3-丁炔-1-醇 | CAS号61541-20-6 methyl 4-hydrox... | CAS号42023-17-6 3-[(dimethylami... | CAS号3140-73-6 2-氯-4,6-二甲氧基-1,... | CAS号124-40-3 二甲胺 | CAS号54509-73-8 ethene | CAS号79-10-7 丙烯酸 | CAS号109-94-4 甲酸乙酯 | CAS号50-00-0 甲醛 | CAS号22122-36-7 3-甲基-2-(5H)-呋喃酮 | CAS号5837-78-5 惕各酸乙酯 | CAS号126812-13-3 methyl 3-(2-oxo... | CAS号1530-62-7 2(3H)-Furanone,... | CAS号13423-15-9 3-甲基四氢呋喃 | CAS号1679-47-6 ALPHA-甲基-GAMMA-丁内酯 | CAS号55341-13-4 3-methyl-2-oxo-... | CAS号119102-90-8 7-苄基-2-噁-7-氮杂螺[... | CAS号76220-95-6 3-Methylene-2-P...

合成工艺路线路线简述

  • 合成目标产物 Tulipalin A 主要起始原料 2(3H)-Furanone, 3-[(Dimethylamino)Methyl]Dihydro- And 2-Chloro-4,6-Dimethoxy-1,3,5-Triazine And Dimethylamine
  • (文献来源)合成步骤主要原料 2(3H)-Furanone, 3-[(Dimethylamino)Methyl]Dihydro- 和 2-Chloro-4,6-Dimethoxy-1,3,5-Triazine 和 Dimethylamine
α-Hydroxymethyl-γ-Butyrolactone置于aluminum Oxide体系中,化学反应生成 2-甲烯基丁内酯
参考文献:Lactone Derivatives And Method Of Making
标题:Lactone Derivatives And Method Of Making

海关参考信息

专利信息


专利号:WO-2025053792-A1
优先权日:2023-09-06
标题:Collective synthesis of phantomolin family through total synthesis of the sesquiterpene lactone molephantin
发明人:CHIBA SHUNSUKE; PATOURET REMI HENRI LOUIS; LI HOI YEUNG; LAI SOAK KUAN
权利人:UNIV NANYANG TECH
摘要:Disclosed herein are processes to generate an intermediate in the total synthesis of (+)- molephantin or a derivative thereof, and a total synthesis of (+)-molephantin or a derivative thereof. Also disclosed herein are methods of forming a compound of formula XIV and of forming a compound of formula XV, wherein compound of formula XIV and compound of formula XV are as defined in the description.

专利号:US-11629223-B2
优先权日:2018-01-11
标 题:Synthesis of polymers from cyclic diolides
发明人:CHEN EUGENE Y; TANG XIAOYAN
权利人:UNIV COLORADO STATE RES FOUND
摘要:Biodegradable polymers with advantageous physical and chemical properties are described, as well as methods for making such polymers. In one embodiment, a new chemical synthesis route to technologically important biodegradable poly(3-hydroxybutyrate) (P3HB) with high isotacticity and molecular weight required for a practical use is described. The new route can utilize racemic eight-membered cyclic diolide (rac-DL), meso-DL, or a rac-DL and meso-DL mixture, derived from bio-sourced dimethyl succinate, and enantiomeric (R,R)-DL and (S,S)-DL, optically resolved by metal-based catalysts. With a stereoselective racemic molecular catalyst, the ROP of rac-DL under ambient conditions produces rapidly P3HB with essentially perfect isotacticity ([mm]>99%), high crystallinity and melting temperature (T m =171° C.), as well as high molecular weight and low dispersity (M n =1.54×10 5 g/mol, Ã?=1.01).

专利号:US-2024425890-A1
优先权日:2022-02-11
标 题:Process for the synthesis of alpha-methylene-gamma-butyrolactone
发明人:TADEN ANDREAS; BECK HORST; MYRTOLLARI KAMELA; KOURIST ROBERT; NIGL ANDREA
权利人:HENKEL AG & CO KGAA
摘要:The present application provides a process for the preparation of α-methylene-γ-butyrolactone, said process comprising the steps of:a) acetylating the C1-hydroxyl group of isoprenol to yield isoprenyl acetate;b) forming 4-acetoxy-2-methylene-butan-1-ol from said isoprenyl acetate by whole cell biotransformation, said step comprising:i) contacting a cell (CB) with a culture medium containing said isoprenyl acetate or with a culture medium contiguous with an organic phase containing said isoprenyl acetate under conditions that enable the cell to form 4-acetoxy-2-methylene-butan-1-ol from isoprenyl acetate; and,ii) optionally isolating the resultant 4-acetoxy-2-methylene-butan-1-ol, wherein said cell (CB) exhibits activity of at least one alkane monooxygenase enzyme which catalyzes the formation of 4-acetoxy-2-methylene-butan-1-ol from isoprenyl acetate;c) oxidizing said 4-acetoxy-2-methylene-butan-1-ol to yield 4-acetoxy-2-methylene butyric acid; and,d) converting said 4-acetoxy-2-methylene butyric acid to α-methylene-γ-butyrolactone by hydroxylysis to γ-hydroxy-α-methylenebutyric acid and subsequent cyclization of said γ-hydroxy-α-methylenebutyric acid.

专利号:US-7164033-B2
优先权日:2004-07-27
标题 :Gas phase synthesis of methylene lactones using novel catalyst
发明人:HUTCHENSON KEITH W; KOURTAKIS KOSTANTINOS; MANZER LEO ERNST
权利人:DU PONT
摘要:Process for converting certain lactones to their alpha-methylene substituted forms that not only exhibits high initial activity (conversion), but also maintains a high level of activity with time on stream.

专利号:US-7348442-B2
优先权日:2004-10-18
标题 :Gas phase synthesis of methylene lactones using catalysts derived from hydrotalcite precursors
发明人:MANZER LEO ERNEST; KOURTAKIS KOSTANTINOS
权利人:DU PONT
摘要:Process for converting certain lactones to their alpha-methylene substituted forms using (i) a catalyst derived from a hydrotalcite or (ii) a composite catalyst comprising the hydrotalcite-derived catalyst into which at least one of lithium, sodium, potassium, rubidium, cesium, magnesium, calcium, strontium, barium has been incorporated.

专利号:EP-2647639-A1
优先权日:2012-04-06
标题:ß-boration of alkene and alkyne intermediates
权利人:LEK PHARMACEUTICALS
摘要:The present invention relates to the field of organic chemistry, and in particular to the preparation of β-borated compounds. These β-borated compounds can be used as intermediates in the synthesis of pharmaceutically active agents such as Sitagliptin.
杭州瑞树生化有限公司
⚠️ 未注册 · 未认证企业
⚠️ 该商家尚未完成注册及企业认证,请用户仔细辨别,谨慎交易。
数据来源于公开网络搜索,平台未作核实,请自行辨别。
🏢敬请 企业认领
🏬开设公司展台
📢获取免费会员权益
🎖️点亮专属注册企业标签
📇展现公司完整信息 样本查看立即注册认领 →
网址: http://www.great-forest.com
企业联系电话:0571-28313180,28313181👤
📞杭州瑞树生化有限公司 ⚠️参考联系方式
联系人:李小玲
电话:0571-28313180,28313181
手机:17767135330
传真:0571-28313182
邮箱:info@great-forest.com
通信地址: 杭州市余杭区仓前镇文一西路1378号,F座,909-913室
邮编: 311121
🆔 联系时候可告知是从"百琢研"平台获取的信息.
⚠️ 声明: 该企业未认证、未认领,请自行辨别信息的真实性和可靠性。咨询或交易时请注意风险评估与信息核实,百琢研不参与任何交易。企业认领注册入口→

地址:杭州市余杭区仓前镇文一西路1378号,F座,909-913室
⚠️ 未注册 · 未认证企业
注册入口 备注: 📌 数据来源说明:本展台内容基于各搜索引擎等公开数据整理,仅作展示用途。请用户自行辨别
✉️ 若企业需抹除展台内容或有异议, 请通过页面底部联系方式告知我们,我们会尽快处理。
铜陵立事达化学科技有限公司
⚠️ 未注册 · 未认证企业
⚠️ 该商家尚未完成注册及企业认证,请用户仔细辨别,谨慎交易。
数据来源于公开网络搜索,平台未作核实,请自行辨别。
🏢敬请 企业认领
🏬开设公司展台
📢获取免费会员权益
🎖️点亮专属注册企业标签
📇展现公司完整信息 样本查看立即注册认领 →
网址: http://www.lishidachem.cn
企业联系电话:18606623089;19064063435👤
📞铜陵立事达化学科技有限公司 ⚠️参考联系方式
联系人:瞿先生;刘经理
电话:18606623089;19064063435
手机:18606623089;19064063435

邮箱:350737036@qq.com
通信地址: 安徽省铜陵市郊区陈瑶湖镇其凤村向东路192号
邮编: 244061
🆔 联系时候可告知是从"百琢研"平台获取的信息.
⚠️ 声明: 该企业未认证、未认领,请自行辨别信息的真实性和可靠性。咨询或交易时请注意风险评估与信息核实,百琢研不参与任何交易。企业认领注册入口→

地址:安徽省铜陵市郊区陈瑶湖镇其凤村向东路192号
⚠️ 未注册 · 未认证企业
注册入口 备注: 📌 数据来源说明:本展台内容基于各搜索引擎等公开数据整理,仅作展示用途。请用户自行辨别
✉️ 若企业需抹除展台内容或有异议, 请通过页面底部联系方式告知我们,我们会尽快处理。
北京偶合科技有限公司
⚠️ 未注册 · 未认证企业
⚠️ 该商家尚未完成注册及企业认证,请用户仔细辨别,谨慎交易。
数据来源于公开网络搜索,平台未作核实,请自行辨别。
🏢敬请 企业认领
🏬开设公司展台
📢获取免费会员权益
🎖️点亮专属注册企业标签
📇展现公司完整信息 样本查看立即注册认领 →
网址: http://www.ouhechem.com
企业联系电话:010-51280831(不占线);010-82967028👤
📞北京偶合科技有限公司 ⚠️参考联系方式
联系人:刘先生
电话:010-51280831(不占线);010-82967028
手机:13911808554
传真:010-82967029
邮箱:sales@ouhechem.com
通信地址: 北京市海淀区西三旗桥东上奥世纪2b-1328室
邮编: 100096
🆔 联系时候可告知是从"百琢研"平台获取的信息.
⚠️ 声明: 该企业未认证、未认领,请自行辨别信息的真实性和可靠性。咨询或交易时请注意风险评估与信息核实,百琢研不参与任何交易。企业认领注册入口→

地址:北京市海淀区西三旗桥东上奥世纪2b-1328室
⚠️ 未注册 · 未认证企业
注册入口 备注: 📌 数据来源说明:本展台内容基于各搜索引擎等公开数据整理,仅作展示用途。请用户自行辨别
✉️ 若企业需抹除展台内容或有异议, 请通过页面底部联系方式告知我们,我们会尽快处理。
第 1 / 1 页

供应商参考报价(招募中)

品牌试剂参考报价(招募中)

📌 第三方产品分析报告

✅ COA系统入驻 | 共享模式

合成参考文献


摘要:Gandon, V.; Thorimbert, S.; Malacria, M., Science of Synthesis, (2009) 46, 197.
摘要:Michalak, M.; Gulajski, L.; Grela, K., Science of Synthesis, (2010) 47, 340.
摘要:Clarke, M. L.; Fuentes, J. A., Science of Synthesis: C-1 Building Blocks in Organic Synthesis, (2013) 1, 404.
参考文献:10.1016/s0223-5234(02)01354-5
摘要:Lee KH, Huang BR. Synthesis and cytotoxic evaluation of alpha-methylene-gamma-butyrolactone bearing naphthalene and naphtho[2,1-b]furan derivatives. Eur J Med Chem. 2002 Apr;37(4):333–8. doi: 10.1016/s0223-5234(02)01354-5.
参考文献:10.1021/jo702563n
摘要:Melsa P, Cajan M, Havlas Z, Mazal C. Substituent effect on exo stereoselectivity in the 1,3-Dipolar cycloaddition reaction of tulipalin A with nitrile ylides. J Org Chem. 2008 Apr 18;73(8):3032–9. doi: 10.1021/jo702563n.
📝 需求与反馈
尽可能描述清楚需求与问题信息
×

通知