CAS: 14542-12-2; Thiazol-2-Ylmethanol

该化合物是一种环环乙醇,具有硫化环核,在2号位置有氢氧化甲基替代物,该化合物是有机合成的多种中间体,特别是在开发药品,农用化学品和功能材料方面,其硫化物具有电子富含和协调特性,而氢氧化硫组则增加了进一步衍生的再生活动,如酯化或乙化.该化合物在标准条件下表现出良好的稳定性,便于处理和储存.其结构特征使得它对于建造生物活性分子,包括抗微生物剂和抗病毒剂具有价值.高纯度等级可用于研究和工业应用,确保合成工作流程的一致性.

结构式图片

相似化合物

10200-59-6 14190-59-1 55842-56-3

欧盟法规

ECHA物质C&L通报

上下游产品

CAS号10200-59-6 2-甲酰基噻唑 | CAS号14527-42-5 噻唑-2-羧酸乙酯 | CAS号50-00-0 甲醛 | CAS号16733-85-0 1,3-噻唑-2-羧胺 | CAS号288-47-1 噻唑 | CAS号40610-14-8 lithium,2H-1,3-... | CAS号3029-48-9 Thi°Cyanic acid... | CAS号3364-78-1 2-氯甲基噻唑 | CAS号10200-59-6 2-甲酰基噻唑 | CAS号131654-56-3 2-溴甲基噻唑

合成工艺路线路线简述

    2-醛基噻唑置于甲醇,Sodium Tetrahydroborate体系中,化学反应 1.0H,以95%的收率获得2-羟甲基噻唑
    参考文献:新型含恶唑单元喹唑啉类似物的设计,合成和生物活性评估
    标题:新型含恶唑单元喹唑啉类似物的设计,合成和生物活性评估
    摘要:以喹唑啉为骨架,恶唑骨架为取代基,设计合成了一种新型的喹唑啉衍生物,并对其生物学活性进行了抗增殖活性和egfr抑制能力的评价.化合物12B表现出最强的抑制活性(对egfr的ic 50 = 0.95 µmol / L),可以在进一步的研究中将其优化为潜在的egfr抑制剂.合成的喹唑啉类似物和所有中间体的结构通过1 H和13 C NMR,2D NMR光谱,Ir光谱和ms光谱确认.
    Doi:10.1002/cjoc.201400271

    海关参考信息

    专利信息


    专利号:US-2004018598-A1
    优先权日:2000-05-30
    标题 :Bio-intermediates for use in the chemical synthesis of polyketides
    发明人:SANTI DANIEL; ASHLEY GARY; MYLES DAVID C
    摘要:The present invention relates to compounds made by a subset of modules from one or more polyketide synthase (“PKSâ€?) genes that are used as starting material in the chemical synthesis of novel molecules, particularly naturally occurring polyketides or derivatives thereof. The biologically derived intermediates (“bio-intermediatesâ€?) generally represent particularly difficult compounds to synthesize using traditional chemical approaches due to one or more stereocenters. In one aspect of the invention, an intermediate in the synthesis of epothilone is provided that feeds into the synthetic protocol of Danishefsky and co-workers. In another aspect of the invention, intermediates in the synthesis of discodermolide are provided that feed into the synthetic protocol of Smith and co-workers. By taking advantage of the inherent stereochemical specificity of biological processes, the syntheses of key intermediates and thus the overall syntheses of compounds like epothilone and discodermolide are greaty simplified.

    专利号:US-8513429-B2
    优先权日:2002-08-23
    标 题:Synthesis of epothilones, intermediates thereto and analogues thereof
    发明人:DANISHEFSKY SAMUEL J; RIVKIN ALEXEY; FUMIKIKO YOSHIMURA; CHOU TING-CHAO; GABARDA ANA E; DONG HUAJIN
    权利人:DANISHEFSKY SAMUEL J; RIVKIN ALEXEY; FUMIKIKO YOSHIMURA; CHOU TING-CHAO; GABARDA ANA E; DONG HUAJIN; SLOAN KETTERING INSITUTE FOR CANCER RES
    摘要:The present invention provides compounds of formula (I): n n n n n n n n n n n n as described generally and in classes and subclasses herein. The present invention additionally provides pharmaceutical compositions comprising compounds of formula (I) and provides methods of treating cancer comprising administering a compound of formula (I).

    专利号:US-7875638-B2
    优先权日:2002-08-23
    标题:Synthesis of epothilones, intermediates thereto, analogues and uses thereof
    发明人:DANISHEFSKY SAMUEL J; RIVKIN ALEXEY; YOSHIMURA FUMIHIKO; CHOU TING-CHAO; GABARDA ANA E; DONG HUAJIN; WU KAIDA; MOORE MALCOLM A S; DORN DAVID
    权利人:SLOAN KETTERING INST CANCER
    摘要:The present invention provides compounds of formula (I): n n n n n n n n n n n n as described generally and in classes and subclasses herein. The present invention additionally provides pharmaceutical compositions comprising compounds of formula (I) and provides methods of treating cancer comprising administering a compound of formula (I).

    专利号:US-7384964-B2
    优先权日:2002-08-23
    标题:Synthesis of epothilones, intermediates thereto, analogues and uses thereof
    发明人:DANISHEFSKY SAMUEL J; RIVKIN ALEXEY; YOSHIMURA FUMIHIKO; CHOU TING-CHAO; GABARDA ANA E; DONG HUAJIN; WU KAIDA; MOORE MALCOLM A S; DORN DAVID
    权利人:SLOAN KETTERING INST CANCER
    摘要:The present invention provides compounds of formula (I): n nas described generally and in classes and subclasses herein. The present invention additionally provides pharmaceutical compositions comprising compounds of formula (I) and provides methods of treating cancer comprising administering a compound of formula (I).

    专利号:US-6921769-B2
    优先权日:2002-08-23
    标题:Synthesis of epothilones, intermediates thereto and analogues thereof
    发明人:DANISHEFSKY SAMUEL J; RIVKIN ALEXY; YOSHIMURA FUMIKIKO; CHOU TING-CHAO; GABARDA ANA E
    权利人:SLOAN KETTERING INST CANCER
    摘要:The present invention provides compounds of formula (I): n n as described generally and in classes and subclasses herein. The present invention additionally provides pharmaceutical compositions comprising compounds of formula (I) and provides methods of treating cancer comprising administering a compound of formula (I).

    专利号:US-2004053995-A1
    优先权日:2002-08-23
    标 题:Synthesis of epothilones, intermediates thereto and analogues thereof
    天津瑞发化工科技发展有限公司
    ⚠️ 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.refinechemicals.com
    企业联系电话:+86-22-87899130👤
    📞天津瑞发化工科技发展有限公司 ⚠️参考联系方式
    联系人:张先生
    电话:+86-22-87899130
    手机:18114031056
    传真:+86-22-87899129
    邮箱:sales@refinechemicals.com
    通信地址: 天津市科研西路12号
    邮编: 300192
    🆔 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:天津市科研西路12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。
    第 1 / 1 页
    现货

    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:Kikelj, D.; Urleb, U., Science of Synthesis, (2002) 11, 799.
    📝 需求与反馈
    尽可能描述清楚需求与问题信息
    ×

    通知