CAS: 823-96-1; Trimethylboroxine

该化合物是一种循环有机体化合物,其分子式为C3H9B3O3. 它的特点是六人分的原生霉毒素环结构,其交替的原生霉素和氧原子与附于每个原生虫中心的甲基组相连.该化合物在有机合成中被广泛用作前体或催化剂,特别是在交叉反应和聚合过程中.在受控制条件下,其高反应性和稳定性使原生原试剂的应用具有价值.三甲基原生霉毒素还用于材料科学,用于制备含有原生碳聚合物和陶瓷,其明确界定的结构和高效的原生化特性提高了合成方法的精确性.由于对水的敏感性,需要妥善处理.

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

trimethylborane water Dimethylborinsaeure-anhydrid dibromomethylboranetriisobutylborane (methyl)difluoroborane 1-methyl-1-vinylcyclohexane n-propylidenecyclohexane

合成工艺路线路线简述

  • 13061-96-6 = 823-96-1
    反应条件:1.1 Reagents: Calcium Hydride Solvents: Diethyl Ether
    标题:Calcium Hydride
    作者:Gawley,Robert E.; Et Al
    参考文献:E-Eros Encyclopedia Of Reagents For Organic Synthesis 日期:2001 卷标:1 页码:1-2]

    13061-96-6 = 823-96-1 [标题:Reaction Conditions
    标题:Product Subclass 8: Boroxanes
    作者:Periasamy,M.; Et Al
    参考文献:Science Of Synthesis 日期:2004 卷标:6 页码:301-320]

    13292-87-0 = 823-96-1
    反应条件:1.1 Catalysts: Tetrabutylammonium Borohydride Solvents: Tetrahydrofuran1.2 Solvents: Acetone
    标题:Organoboranes. 39. Convenient Procedures For The Preparation Of Methylboronic Acid And Trimethylboroxin
    作者:Brown,Herbert C.; Et Al
    参考文献:Organometallics 日期:1985 卷标:4(5) 页码:816-21]

    917-54-4 = 823-96-1
    反应条件:1.1 Reagents: Triisopropyl Borate Solvents: Diethyl Ether1.2 Reagents: Hydrochloric Acid1.3 Reagents: Water2.1 Reagents: Calcium Hydride
    标题:Organoboranes. 39. Convenient Procedures For The Preparation Of Methylboronic Acid And Trimethylboroxin
    作者:Brown,Herbert C.; Et Al
    参考文献:Organometallics 日期:1985 卷标:4(5) 页码:816-21]

    47855-94-7 = 823-96-1 + 47855-94-7
    反应条件:1.1 Reagents: Triphenylmethane Solvents: 1,2-Dichlorobenzene; 2 Atm,-78 °C; 24 H,20 °C
    标题:Complete Reductive Cleavage Of Co Facilitated By Highly Electrophilic Borocations
    作者:Curless,Liam D.; Et Al
    参考文献:Chemical Communications (Cambridge 日期:2015 卷标:51(54) 页码:10903-10906]

    = 823-96-1 [标题:Reaction Conditions
    标题:Oxo(Trisyl)Borane (Me3Si)3C-Bo As An Intermediate
    作者:Paetzold,Peter; Et Al
    参考文献:Zeitschrift Fuer Anorganische Und Allgemeine Chemie 日期:1995 卷标:621(5) 页码:732-6]

    47855-94-7 = 823-96-1 + 47855-94-7
    反应条件:1.1 Reagents: Triphenylmethane Solvents: 1,2-Dichlorobenzene; 2 Atm,-78 °C; 100 °C
    标题:Complete Reductive Cleavage Of Co Facilitated By Highly Electrophilic Borocations
    作者:Curless,Liam D.; Et Al
    参考文献:Chemical Communications (Cambridge 日期:2015 卷标:51(54) 页码:10903-10906]

    = 823-96-1 [标题:Reaction Conditions
    标题:Product Subclass 8: Boroxanes
    作者:Periasamy,M.; Et Al
    参考文献:Science Of Synthesis 日期:2004 卷标:6 页码:301-320]

    1121-48-8 = 823-96-1
    反应条件:1.1 Solvents: Diethyl Ether2.1 Reagents: Calcium Hydride
    标题:Organoboranes. 39. Convenient Procedures For The Preparation Of Methylboronic Acid And Trimethylboroxin
    作者:Brown,Herbert C.; Et Al
    参考文献:Organometallics 日期:1985 卷标:4(5) 页码:816-21]

    1722-26-5 + 47855-94-7 + 13948-08-8 = 823-96-1 + 47855-94-7
    反应条件:1.1 Solvents: 1,2-Dichlorobenzene,Dmso-D6; 10 Min,Rt2.1 Reagents: Triphenylmethane Solvents: 1,2-Dichlorobenzene; 2 Atm,-78 °C; 100 °C
    标题:Complete Reductive Cleavage Of Co Facilitated By Highly Electrophilic Borocations
    作者:Curless,Liam D.; Et Al
    参考文献:Chemical Communications (Cambridge 日期:2015 卷标:51(54) 页码:10903-10906]

    88996-23-0 + 47855-94-7 + 13948-08-8 = 823-96-1 + 47855-94-7
    反应条件:1.1 Solvents: 1,2-Dichlorobenzene,Dmso-D6; 10 Min,Rt2.1 Reagents: Triphenylmethane Solvents: 1,2-Dichlorobenzene; 2 Atm,-78 °C; 24 H,20 °C
    标题:Complete Reductive Cleavage Of Co Facilitated By Highly Electrophilic Borocations
    作者:Curless,Liam D.; Et Al
    参考文献:Chemical Communications (Cambridge 日期:2015 卷标:51(54) 页码:10903-10906]

    = 823-96-1
    反应条件:1.1 Solvents: Pentane2.1 -
    标题:Oxo(Trisyl)Borane (Me3Si)3C-Bo As An Intermediate
    作者:Paetzold,Peter; Et Al
    参考文献:Zeitschrift Fuer Anorganische Und Allgemeine Chemie 日期:1995 卷标:621(5) 页码:732-6]

    5158-50-9 = 823-96-1
    反应条件:1.1 -2.1 Solvents: Pentane3.1 -
    标题:Oxo(Trisyl)Borane (Me3Si)3C-Bo As An Intermediate
    作者:Paetzold,Peter; Et Al
    参考文献:Zeitschrift Fuer Anorganische Und Allgemeine Chemie 日期:1995 卷标:621(5) 页码:732-6
三甲基硼置于boron Trioxide体系中,化学反应生成 三甲基环三硼氧烷
参考文献:Goubeau; Keller,Zeitschrift Fur Anorganische Und Allgemeine Chemie,1951,Vol. 267,P. 5,20
标题:Goubeau; Keller,Zeitschrift Fur Anorganische Und Allgemeine Chemie,1951,Vol. 267,P. 5,20

专利信息


专利号:US-7973171-B2
优先权日:2005-06-13
标题:Process for synthesis of dialkoxyorganoboranes
发明人:BURKHARDT ELIZABETH; ATKINS WILLIAM
权利人:BURKHARDT ELIZABETH; ATKINS WILLIAM
摘要:The invention relates to a process for the synthesis of dialkoxyorganoboranes, in particular to a process for the synthesis of dialkoxyorganoboranes by an ester exchange reaction. Moreover, the invention relates to a process for the synthesis of organo-oxazaborolidine catalysts (organo-CBS) and of trialkylboroxins. Furthermore, the invention relates to methods of using dialkoxyorganoboranes for the preparation of organo-CBS catalysts and in Suzuki-type coupling reactions.

专利号:US-8258299-B2
优先权日:2009-03-27
标题:Process for preparation of temsirolimus
发明人:LEE KWANG-CHUNG; LEE TING-HUEI; TUNG YEN-SHIH; KAO CHIA-CHEN; LEE TZU-AI
权利人:LEE KWANG-CHUNG; LEE TING-HUEI; TUNG YEN-SHIH; KAO CHIA-CHEN; LEE TZU-AI; CHUNGWA CHEMICAL SYNTHESIS & BIOTECH CO LTD
摘要:The present invention provides two synthetic routes for the preparation of Temsirolimus (compound 1b and analog of Temsirolimus 1a). The first route includes the synthesis of CCI-779 by directly reacting rapamycin (4b) or Prolyl-rapamycin (4a) with substituent-2,2-bis(methoxy) propionic acid anhydride(11) in the presence of an organic base, followed by deprotection to give CCI-779 or Proline CCI-779. The second route includes a process involving a reaction of rapamycin-OH-31-sily ether (4d) or Prolyl-rapamycin-OH-31-sily ether (4c) with substituent-2,2-bis(methoxy) propionic acid anhydride(11) in the presence of an organic base and followed by subsequent hydrolysis step to obtain the desired CCI-779 or Proline CCI-779. n Compound 11, as described in this invention, is stable at room temperature, cost effective and ease of processing.

专利号:US-6765117-B2
优先权日:1997-10-24
标题:Process for stereoselective synthesis of prostacyclin derivatives
发明人:MORIARTY ROBERT M; PENMASTA RAJU; GUO LIANG; RAO MUNAGALA S; STASZEWSKI JAMES P
权利人:UNITED THERAPEUTIC CORP
摘要:An improved method is described for making 9-deoxy-PGF 1 -type compounds. In contrast to the prior art, the method is stereoselective and requires fewer steps than the known methods for making these compounds. The invention also relates to novel intermediates prepared during the synthesis of the 9-deoxy-PGF 1 -type compounds.

专利号:US-2025115551-A1
优先权日:2023-10-03
标 题:Synthesis of ras inhibitors
发明人:LI YI; MENDOZA BENJAMIN; NAGANATHAN SRIRAM; WANG ROSS; YI YI; BALLMER STEVEN G; DAVIDSON JAMES; HUANG XIAOJUN
权利人:REVOLUTION MEDICINES INC
摘要:The present invention relates to Ras inhibitors, intermediates in the synthesis thereto, and methods for preparing the Ras inhibitors and the intermediates.

专利号:US-6096883-A
优先权日:1996-05-31
标 题 :3-hydroxy gamma-lactone based enantioselective synthesis of azetidinones
发明人:WU GEORGE G; CHEN XING; WONG YEE-SHING; SCHUMACHER DORIS P; STEINMAN MARTIN
权利人:SCHERING CORP
摘要:The invention relates to intermediates of the formulae ##STR1## said intermediates being useful in a process for producing a compound of the formula ##STR2## wherein Bn is benzyl and R 1 , 2 and R 3 are as defined in the specification,

专利号:WO-9842627-A1
优先权日:1997-03-20
标题 :Sol-gel synthesis of alkali-free borosilicate glass
发明人:VARMA KARIKATH SUKUMAR
权利人:PILKINGTON PLC; VARMA KARIKATH SUKUMAR
摘要:A method of producing metalloborates (including silicoborates) comprising reacting a trisubstituted boroxine with a tetrasubstituted orthosilicate or metal alkoxide in the substantial absence of hydroxyl groups to form a sol-gel so that the rate of reaction may be controlled and that the time taken for the reaction mixture to form a gel is substantially increased. The reaction may be carried out in the presence of a solvent and of a catalyst.
上海福兴医药科技有限公司
⚠️ 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.forxine.com
企业联系电话:021-64961388,64961699👤
📞上海福兴医药科技有限公司 ⚠️参考联系方式
联系人:张经理
电话:021-64961388,64961699
手机:18918697718
传真:021-64961388-8320
邮箱:service@forxine.com
通信地址: 上海市闵行区都会路1835号
邮编: 201108
🆔 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:上海市闵行区都会路1835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。
常州市宣明医药科技有限公司
⚠️ 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://xuanmingchem.com
企业联系电话:0519-85525329👤
📞常州市宣明医药科技有限公司 ⚠️参考联系方式
联系人:刘明;许雯
电话:0519-85525329
手机:15951231113;13646117943
传真:0519-85190960
邮箱:sales@xuanmingchem.com
通信地址: 江苏省常州市新北区汉江路120号
邮编: 213000
🆔 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:江苏省常州市新北区汉江路120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。
霸州市路德精细化工有限公司
⚠️ 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.bzlude.com
电话: 0316-735501618632660479👤
📞霸州市路德精细化工有限公司 ⚠️参考联系方式

销售电话:0316-735501618632660479
邮箱:bzlude@163.com
🆔 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→

⚠️ 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。
威智医药股份有限公司
⚠️ 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.viwit.com
企业联系电话:0632-2980981;15063270987👤
📞威智医药股份有限公司 ⚠️参考联系方式
联系人:翁经理
电话:0632-2980981;15063270987
手机:15063270987
传真:QQ2730058784
邮箱:service.china3@viwit.com
通信地址: 山东省滕州市生物医药产业基地威智大道88号
邮编: 277514
🆔 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:山东省滕州市生物医药产业基地威智大道88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:Toyota, S.; Iwanaga, T., Science of Synthesis, (2010) 45, 782.
摘要:Kalyani, D.; Desai, L. V., Science of Synthesis: Cross Coupling and Heck-Type Reactions, (2012) 3, 758.
摘要:Molander, G. A.; Ryu, D., Science of Synthesis: C-1 Building Blocks in Organic Synthesis, (2013) 2, 34.
摘要:Molander, G. A.; Ryu, D., Science of Synthesis: C-1 Building Blocks in Organic Synthesis, (2013) 2, 35.
摘要:Yi, C. S., Science of Synthesis: Catalytic Transformations via CH Activation, (2015) 1, 242.
📝 需求与反馈
尽可能描述清楚需求与问题信息
×

通知