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2-hydroxy-4,5-dimethyl-1,3,2-dioxaborolane

中文名称
——
中文别名
——
英文名称
2-hydroxy-4,5-dimethyl-1,3,2-dioxaborolane
英文别名
2.3-Butylen-hydrogenborat
2-hydroxy-4,5-dimethyl-1,3,2-dioxaborolane化学式
CAS
——
化学式
C4H9BO3
mdl
——
分子量
115.925
InChiKey
GSEPAWDRCIATNR-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):
    -0.21
  • 重原子数:
    8
  • 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:
    38.7
  • 氢给体数:
    1
  • 氢受体数:
    3

反应信息

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文献信息

  • Gmelin Handbuch der Anorganischen Chemie, Gmelin Handbook: B: SVol.1, 4.8.5, page 226 - 230
    作者:
    DOI:——
    日期:——
  • Borylation of calix[4]resorcinols under ultrasonic irradiation
    作者:I. S. Nizamov、R. R. Shamilov、G. R. Sabirzyanova、E. I. Nikitin、A. R. Burilov、M. A. Pudovik
    DOI:10.1134/s107036321205009x
    日期:2012.5
    The use of ultrasonic irradiation in the reactions of trialkyl borates with octahydroxytetraoctyl[l (4)] metacyclophane allowed us obtaining tetraalkoxyboratocavitands with higher yields and under milder conditions. We first obtained 1,3,2-dioxaborolane and 1,3,2-dioxaborinane derivatives of tetraoctyl[l (4)]metacyclophane using ultrasonic irradiation. Boratocavitands were converted into the corresponding amine complexes with isobutylamine.
  • The Borates of 2,3-Butylene Glycol
    作者:S. A. Morell、E. C. Lathrop
    DOI:10.1021/ja01221a507
    日期:1945.5
  • Volatile Borates of Polyhydric Alcohols and the Activation of Boric Acid.
    作者:Ralph Elliott Rippere、Victor K. La Mer
    DOI:10.1021/j150426a003
    日期:1943.3
  • ——
    作者:I. S. Nizamov
    DOI:10.1023/a:1023312406687
    日期:——
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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