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[1,3,2]dioxaborolane | 1942-28-5

中文名称
——
中文别名
——
英文名称
[1,3,2]dioxaborolane
英文别名
1,3,2-dioxaborolane radical;1,3,2-dioxaborolane;<1,3,2>-Dioxaborolan;Aethylenglykolborin;1,3,2-Dioxaborolan;InChI=1/C2H5BO2/c1-2-5-3-4-1/h3H,1-2H
[1,3,2]dioxaborolane化学式
CAS
1942-28-5
化学式
C2H5BO2
mdl
——
分子量
71.8715
InChiKey
NCWDBNBNYVVARF-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    -0.7
  • 重原子数:
    5
  • 可旋转键数:
    0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    18.5
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    参考文献:
    名称:
    Efficient and straightforward preparation of a building block for (−)-teubrevin G synthesis via chemically diversed oriented synthesis
    摘要:
    A rapid and efficient methodology to highly functionalised molecular units well suited as scaffolds for diversity-oriented molecular construction in the synthesis of natural products is reported herein. A key macrocyclic intermediate in the synthesis of the neo-clerodane diterpene (-)-teubrevin G was successfully synthesized in a 5-step sequence in a 70% overall yield using a novel intramolecular coupling between an allylborating agent and a 1,5-dialdehyde moiety. (C) 2011 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2011.10.112
  • 作为产物:
    描述:
    乙二醇 在 sodium tetrahydroborate 、 作用下, 以 四氢呋喃 为溶剂, 生成 [1,3,2]dioxaborolane
    参考文献:
    名称:
    Niedenzu,K. et al., Chemische Berichte, 1972, vol. 105, p. 2258 - 2263
    摘要:
    DOI:
  • 作为试剂:
    描述:
    参考文献:
    名称:
    AZAINDAZOLE COMPOUNDS
    摘要:
    本发明涉及式(I)的吡唑嗪化合物,或其药学上可接受的盐,其中W为CR4或N;R1、R2、R3和R4在此定义。本发明还涉及使用这种化合物治疗至少一种CYP17相关疾病的方法,例如癌症,以及包含这种化合物的制药组合物。
    公开号:
    US20130184254A1
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文献信息

  • METHODS OF TREATING SEROTONIN-MEDIATED DISEASES AND DISORDERS
    申请人:Brown Philip Manton
    公开号:US20090005381A1
    公开(公告)日:2009-01-01
    Methods are disclosed for treating serotonin-mediated diseases and disorders, which comprise inhibiting tryptophan hydroxylase (TPH) in patients in need thereof.
    本发明公开了治疗与血清素有关的疾病和障碍的方法,包括抑制需要此类治疗的患者中的色酸羟化酶(TPH)。
  • Octahydro-pyrrolo[3,4-b]pyrrole Derivatives
    申请人:Cowart D. Marlon
    公开号:US20070232612A1
    公开(公告)日:2007-10-04
    Octahydro-pyrrolo[3,4-b]pyrrole derivatives are useful in treating conditions or disorders prevented by or ameliorated by histamine-3 receptor ligands, Octahydro-pyrrolo[3,4-b]pyrrole compounds, methods for using such compounds, compositions for making them, and processes for preparing such compounds are disclosed herein.
    本文披露了八氢吡咯并[3,4-b]吡咯生物在治疗由组胺-3受体配体预防或改善的疾病或疾患方面的用途,包括八氢吡咯并[3,4-b]吡咯化合物,使用这种化合物的方法,制备它们的组合物以及制备这种化合物的过程。
  • METHODS OF USING AND COMPOSITIONS COMPRISING TRYPTOPHAN HYDROXYLASE INHIBITORS
    申请人:Brown Philip Manton
    公开号:US20090005382A1
    公开(公告)日:2009-01-01
    Methods and compositions comprising tryptophan hydroxylase inhibitors are disclosed. Particular methods are directed at reducing or avoiding serotonin-mediated adverse effects associated with some drugs.
    本发明涉及使用色酸羟化酶抑制剂的方法和组合物。特定的方法旨在减少或避免与某些药物相关的血清素介导的不良反应。
  • METHODS OF AFFECTING GASTROINTESTINAL TRANSIT AND GASTRIC EMPTYING, AND COMPOUNDS USEFUL THEREIN
    申请人:Liu Qingyun
    公开号:US20090029993A1
    公开(公告)日:2009-01-29
    Methods and compounds are disclosed for affecting gastrointestinal motility and gastric emptying, which comprise inhibiting tryptophan hydroxylase (TPH) in patients in need thereof.
    本发明揭示了一种影响胃肠动力和胃排空的方法和化合物,该方法包括抑制需要此类治疗的患者中的色酸羟化酶(TPH)。
  • Methods and Compositions for Treating Pulmonary Hypertension and Related Diseases and Disorders
    申请人:Sands Arthur T.
    公开号:US20090054308A1
    公开(公告)日:2009-02-26
    Methods of treating pulmonary hypertension are disclosed. Particular methods comprise the administration of a tryptophan hydroxylase inhibitor and at least one other active pharmaceutical ingredient to patient in need thereof. Pharmaceutical formulations are also disclosed.
    公开了治疗肺动脉高压的方法。具体方法包括向需要治疗的患者施用色酸羟化酶抑制剂和至少一种其他活性药物成分。还公开了制药配方。
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表征谱图

  • 氢谱
    1HNMR
  • 质谱
    MS
  • 碳谱
    13CNMR
  • 红外
    IR
  • 拉曼
    Raman
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  • 峰位数据
  • 峰位匹配
  • 表征信息
Shift(ppm)
Intensity
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Assign
Shift(ppm)
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测试频率
样品用量
溶剂
溶剂用量
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同类化合物

频那醇硼烷 联硼酸频那醇酯 硼酸频哪醇酯 硼酸环乙醇频哪醇酯 异丙醇频哪醇硼酸酯 双(N,N,N',N'-四甲基-L-酒石酰胺乙二醇基)二硼 双(N,N,N,N-四甲基-D-酒石酰胺二醇酸根)二硼 乙氧基硼酸频哪醇酯 N,N-二甲基-2-[(4,4,5,5-四甲基-1,3,2-二氧杂环戊硼烷-2-基)氧基]乙胺 4,4,5,5-四甲基-1,3,2-二氧杂硼环戊烷-2-基硼酸 4,4',5,5'-四甲基-2,2'-联-1,3,2-二氧硼杂环戊烷 2-羟基-4-十四烷基-1,3,2-二氧硼戊环 2-甲氧基-4,4,5,5-四甲基-1,3,2-二氧硼戊环 2-(甲基氨基)苯基硼酸频哪醇酯 2,2'-[乙烯二(氧基)]二[1,3,2-二氧硼戊环] 1,3,2-二噁硼戊环,2-(1-环戊烯-1-氧基)- 2-(4-tert-butyl-cyclohex-1-enyl)-4,4,5,5-tetramethy-[1,3,2]dioxaborolane 2-(but-3-en-1-yloxy)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 4,8-dimethyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,3,6,2-dioxazaborocane 4-Hydroxymethyl-[1,3,2]dioxaborolan-2-OL 4-(Sulfanylmethyl)-1,3,2-dioxaborolan-2-ol 2-Methoxy-1,3,2-dioxaborolan Ethylen-cyclohexyl-borat isopropenyl pinacol boronic ester dihydroxy-{ethane-1.2-diolato(2-)-O,O'}-borate(1-) bis-(ethane-1,2-diol) borate 4,4,5,5-tetramethyl-2-<(E)-1-methyl-1-propenyloxy>-1,3,2-dioxaborolane 4,5,5-Triaethyl-2-chlormethyl-4-bora-1,3-dioxolan 2-methoxy-1,4-bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,4-dihydropyrazine 4,4,4',4',5,5'-Hexamethyl-2,2'-bi-1,3,2-dioxaborolane ([1,3,2]-dioxaborolan-2-yl)tert-butyldimethylsiloxane Bis(N,N,N',N'-tetramethyl-D-tartaramide glycolato)diboron 2-methylaminoethoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 2-(2'-methylaminoethoxy)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 2-Chlor-4-methyl-1,3,2-dioxaborolan Borsaeure-aethylester-aethylenester N-[1,3,2]dioxaborolan-2-yl-2,2,2-trifluoro-N-methyl-acetamide 2,6-dimethyl-1,4-bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,4-dihydropyrazine (η1-CO2C4H7)B(OCMe2CMe2O) 2-((allylsulfinyl)oxy)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 9-Methyl-1,4,6-trioxa-9-azonia-5-boranuidaspiro[4.4]nonane 2-Fluoro-4-methyl-1,3,2-dioxaborolane 2-Fluoro-1,3,2-dioxaborolane 2-cyano-1,4-bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,4-dihydropyrazine 2-[(But-2-en-2-yl)oxy]-1,3,2-dioxaborolane 2-{2-[(1,3,2-Dioxaborolan-2-yl)oxy]ethoxy}ethan-1-ol 2,2'-[Butane-1,4-diylbis(oxy)]bis(1,3,2-dioxaborolane) (4R)-4-Carboxy-1,3,2-dioxaborolan-2-yl [1,3,2]dioxaborolane 2,2'-oxy-bis-[1,3,2]dioxaborolane