CAS: 5158-50-9; Bromodimethylborane

该化合物是一种有机有机体化合物,广泛用于有机合成和交叉组合反应,其主要优点包括高活性,作为极电子极原来源,能够对丙烯和烷基亚基质进行高效的博照,该化合物在铃木-米亚乌拉和其他催化联结中特别宝贵,因为它在温和条件下具有稳定性和控制的再活性.此外,其室温液体状态有利于实验室环境中的精确处理和剂量.溴甲基丙烷还被用于合成含有钴的聚合物和先进材料,在学术和工业应用中提供多用途.建议在惰性条件下进行适当的处理,因为其湿度敏感.

结构式图片

欧盟法规

ECHA物质C&L通报

上下游产品

CAS号593-90-8 甲基硼 | CAS号10294-33-4 三溴化硼 | CAS号594-27-4 四甲基锡 | CAS号27484-88-4 bis(dimethylbor... | CAS号17933-16-3 Dibromo(methyl)... | CAS号137516-91-7 2,4,6-trimethyl... | CAS号137516-92-8 (2,6-diisopropy... | CAS号75-24-1 三甲基铝 | CAS号1113-22-0 Ethyldimethylborane | CAS号19163-16-7 [[bis(dimethylb... | CAS号19163-15-6 N,N-bis(dimethy... | CAS号593-90-8 甲基硼 | CAS号5314-85-2 Borazine, 2,4,6... | CAS号19163-05-4 Borinic acid, d... | CAS号2857-97-8 三甲基溴硅烷 | CAS号42452-07-3 N-(dimethylthio... | CAS号42452-09-5 | CAS号42452-11-9 dimethylboranyl...

合成工艺路线路线简述

    📜三甲基铝置于三溴化硼体系中,化学反应生成 二甲基溴化硼
    参考文献:Goubeau In W.Klemm,Anorganische Chemie,Tl. I (=naturf.Med.Dtschld. 1939-1946,Bd.23)S.235
    标题:Goubeau In W.Klemm,Anorganische Chemie,Tl. I (=naturf.Med.Dtschld. 1939-1946,Bd.23)S.235

    专利信息


    专利号:US-11220513-B2
    优先权日:2015-04-30
    标题:Chromium-mediated coupling and application to the synthesis of halichondrins
    发明人:KISHI YOSHITO; YAN WUMING; LI JINGWEI; LI ZHANJIE; YAHATA KENZO
    权利人:HARVARD COLLEGE
    摘要:The present invention provides unified synthesis of the C1-C19 building blocks of halichondrins and analogs thereof using selective coupling of poly-halogenated nucleophiles in chromium-mediated coupling reactions. The present invention also provides a practical and efficient synthesis of C20-C38 building blocks of halichondrins and analogs thereof. Also provided herein are general methods of selective activation and coupling of poly-halogenated analogs with an aldehyde. The provided coupling reactions are selective for halo-enone and halo-acetylenic ketal over vinyl halide and halide attached to a sp hybridized carbon. The provided efficient selective coupling reactions can allow easy access to the C1-C19 building blocks and C20-C38 building blocks of halichondrins and analogs thereof with limited or no purification or separation of the intermediates.

    专利号:WO-2025108575-A1
    优先权日:2023-11-21
    标 题:Methods of selective deprotection and synthesis of transhydrindane- skeleton-based compounds
    发明人:HUBER FLORIAN MAURITIUS ERASMUS
    权利人:ROCHE DIAGNOSTICS GMBH
    摘要:The present invention relates to methods of selectively deprotecting a transhydrindane-skeleton-based compound comprising at least two different silyl ether groups. The present invention further relates to methods of synthesizing a Vitamin D molecule and to Vitamin D molecules obtainable by such processes. Furthermore, the present invention relates to a compound according to formula (I) comprising two different silyl ether groups, its use in the synthesis of Vitamin D molecules and to methods of producing such a compound.

    专利号:US-2007065922-A1
    优先权日:2005-09-21
    标题 :Biocatalytic synthesis of aminodeoxy purine N9-beta-D-nucleosides containing 3-amino-3-deoxy-beta-D-ribofuranose, 3-amino-2,3-dideoxy-beta-D-ribofuranose, and 2-amino-2-deoxy-beta-D-ribofuranose as sugar moieties
    发明人:BARAI VLADIMIR N; EROSHEVSKAYA LUDMILLA A; MIKHAILOPULO IGOR A; AZHAYEV ALEX V; LAPINJOKI SEPPO P
    权利人:METKINEN OY
    摘要:Purine N 9 -β-D-nucleosides containing 3-amino-3-deoxy-β-D-ribofaranose, 3-amino-2,3-dideoxy-β-D-ribofuranose, and 2-amino-2-deoxy-β-D-ribofuranose as sugar moieties are synthesized by biocatalytic transglycosylation of purine bases and the respective 3′-amino-3′-deoxyuridine, 3′-amino-3′-deoxythymidine and 2′-amino-2′-deoxyuridine as donors of the carbohydrate moiety, and the cells of Escherichia coli as a biocatalyst or glutaraldehyde (GA) treated cells of Escherichia coli as a biocatalyst or a mixture of thymidine (uridine) phosphorylase and purine nucleoside phosphorylase.

    专利号:US-10899878-B2
    优先权日:2017-04-06
    标 题:Phosphorus-containing caprolactone monomers for synthesis of flame retardant polycaprolactones
    发明人:CAMPBELL ERIC J; CZAPLEWSKI SARAH K; KOBILKA BRANDON M; WERTZ JASON T
    权利人:IBM
    摘要:A process of forming a flame retardant monomer includes forming a hydroxyl-functionalized caprolactone molecule, and reacting the hydroxyl-functionalized with a phosphorus-containing flame retardant molecule to form a flame retardant-functionalized caprolactone monomer. A flame retardant monomer includes at least one moiety derived from a hydroxyl-functionalized caprolactone molecule and at least one phosphorus-containing flame retardant moiety. A flame retardant polymer includes at least two flame retardant monomer repeat units, each flame retardant monomer repeat unit including at least one moiety derived from a hydroxyl-functionalized caprolactone molecule and at least one phosphorus-containing flame retardant moiety.

    专利号:US-7741473-B2
    优先权日:2005-03-30
    标 题 :Process for the preparation of 4,6-disubstituted-tetrahydro-furo, thieno, pyrrolo and cyclopenta-[3,4][1,3]dioxoles
    发明人:WATSON PAUL S; DOUGLASS III JAMES G; SUCHOZAK BOB; PANDIARAJU SUBRAMANIAN; DIXON CRAIG E; LEVIN DANIEL
    权利人:INSPIRE PHARMACEUTICALS INC
    摘要:The present invention is directed to a processes for the synthesis of trans isomer of 4,6-disubstituted-tetrahydro-furo, thieno, pyrrolo and cyclopenta-[3,4][1,3]dioxoles (Formula I). The process comprises the steps of: (a) obtaining a compound of Formula II, which is a mixture of cis and trans-diastereomers, and (b) chemically decomposing the compound of Formula II in a solution comprising a solvent and an acid that is a hydrogen donor or an electron pair acceptor, whereby the cis diastereomer is decomposed and the compound of Formula I is obtained. The compounds prepared by the present invention are useful in treating diseases or conditions associated with platelet aggregation and/or platelet activation.

    专利号:US-5559237-A
    优先权日:1992-06-05
    标题:Process for preparation of 2-oxo-1-piperidinyl derivatives
    发明人:RANGANATHAN RAMACHANDRAN S; ARUNACHALAM THANGAVEL; NATALIE JR KENNETH J
    权利人:BRACCO INT BV
    摘要:The present process involves ring opening and ring closure of compounds containing a tetrahydrofuroyl to provide facile synthesis of compounds containing a piperidin-2-one group of the formula

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    📌 第三方产品分析报告

    ✅ COA系统入驻 | 共享模式

    合成参考文献


    参考文献:10.1007/s00216-014-7826-4
    摘要:Wensbo Posaric D, Andersson A, Bergquist K, Isaksson A. Differentiation and quantification of synthetic phosphatidylethanol (PEth) homologues by 1H- and 13C-NMR in polar organic solvents. Analytical and Bioanalytical Chemistry. 2014 May 28;406(19):4735–44. doi: 10.1007/s00216-014-7826-4.
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