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2,3-二甲基-1-戊醇 | 10143-23-4

中文名称
2,3-二甲基-1-戊醇
中文别名
2,3-二甲基戊醇
英文名称
2,3-Dimethyl-1-pentanol
英文别名
2,3-dimethylpentanol-1;2,3-dimethyl-pentan-1-ol;2,3-dimethylpentan-1-ol
2,3-二甲基-1-戊醇化学式
CAS
10143-23-4
化学式
C7H16O
mdl
——
分子量
116.203
InChiKey
MIBBFRQOCRYDDB-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

物化性质

  • 熔点:
    -30.45°C (estimate)
  • 沸点:
    147.3°C (estimate)
  • 密度:
    0.8340
  • 物理描述:
    2,3-dimethyl-1-pentanol is a clear colorless liquid. (NTP, 1992)
  • 闪点:
    142 °F (NTP, 1992)
  • 溶解度:
    1 to 5 mg/mL at 72.5° F (NTP, 1992)
  • 蒸汽压力:
    1 mm Hg at 122 °F ; 20 mm Hg at 158° F; 60 mm Hg at 203° F (NTP, 1992)
  • 稳定性/保质期:
    遵循规格进行使用和储存,则不会导致分解。

计算性质

  • 辛醇/水分配系数(LogP):
    2.2
  • 重原子数:
    8
  • 可旋转键数:
    3
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    20.2
  • 氢给体数:
    1
  • 氢受体数:
    1

ADMET

毒理性
  • 副作用
神经毒素 - 急性溶剂综合症
Neurotoxin - Acute solvent syndrome
来源:Haz-Map, Information on Hazardous Chemicals and Occupational Diseases
毒理性
  • 非人类毒性摘录
...在兔眼测试中被评为9分。 ...在兔子的眼睛外部进行测试,并根据24小时后观察到的伤害程度按1-10的等级进行数值评分,特别关注角膜的状况。
...RATED 9 ON RABBIT EYES. ...TESTED EXTERNALLY ON EYES OF RABBITS AND HAVE BEEN RATED NUMERICALLY ON SCALE OF 1-10 ACCORDING TO DEGREE OF INJURY OBSERVED AFTER 24 HR, PAYING PARTICULAR ATTENTION TO CONDITION OF CORNEA.
来源:Hazardous Substances Data Bank (HSDB)

安全信息

  • 危险等级:
    3
  • 危险品运输编号:
    UN 1987
  • 海关编码:
    2905199090
  • 危险类别码:
    R10,R36/37/38
  • 储存条件:
    密封于阴凉干燥处。

SDS

SDS:41b1e61ee693530f81ee90409bc7bd82
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反应信息

  • 作为反应物:
    描述:
    2,3-二甲基-1-戊醇1-Alapha-萘异氰酸酯 生成 [1]naphthyl-carbamic acid-(3,4-dimethyl-pentyl ester)
    参考文献:
    名称:
    Condensation of Saturated Hydrocarbons with Haloölefins. I. The Reaction of Isobutane with Vinyl Chloride and Allyl Chloride1
    摘要:
    DOI:
    10.1021/ja01225a006
  • 作为产物:
    描述:
    1,2-Epoxy-2,3-dimethyl-pentan 在 lithium aluminium tetrahydride 、 三氯化铝 作用下, 以 乙醚 为溶剂, 生成 2,3-二甲基-1-戊醇
    参考文献:
    名称:
    Kirmse,W. et al., Chemische Berichte, 1973, vol. 106, p. 1376 - 1383
    摘要:
    DOI:
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文献信息

  • TOLL LIKE RECEPTOR MODULATOR COMPOUNDS
    申请人:Gilead Sciences, Inc.
    公开号:US20160289229A1
    公开(公告)日:2016-10-06
    The present disclosure relates generally to toll like receptor modulator compounds, such as diamino pyrido[3,2 D]pyrimidine compounds and pharmaceutical compositions which, among other things, modulate toll-like receptors (e.g. TLR-8), and methods of making and using them.
    本公开涉及调节类似受体调节剂化合物,例如二氨基吡啶并[3,2 D]嘧啶化合物和药物组合物,其中调节类似受体(例如TLR-8),以及制备和使用它们的方法。
  • Bioisosteric Exchange of Csp3 -Chloro and Methyl Substituents: Synthesis and Initial Biological Studies of Atpenin A5 Analogues
    作者:Simon Krautwald、Christian Nilewski、Mihoko Mori、Kazuro Shiomi、Satoshi Ōmura、Erick M. Carreira
    DOI:10.1002/anie.201511672
    日期:2016.3.14
    Asymmetric synthesis and initial biological studies of two analogues of a naturally occurring chlorinated antifungal agent, atpeninA5, are described. These analogues were selected on the basis of Cl→CH3 or H3C→Cl exchanges in the side‐chain of atpeninA5. The interchange of chloro and methyl substituents led to complex II inhibitors with equal IC50 values. This suggests that Cl↔Me bioisosteric exchange
    描述了两种天然存在的氯化抗真菌剂,atpenin A5的类似物的不对称合成和初步生物学研究。这些类似物是根据atpenin A5侧链中的Cl→CH 3或H 3 C→Cl交换选择的。氯和甲基取代基的互换产生了具有相同IC 50值的络合物II抑制剂。这表明可以在脂肪族环境中实现Cl↔Me生物立体交换。
  • Identification and Quantification of Aerosol Polar Oxygenated Compounds Bearing Carboxylic or Hydroxyl Groups. 1. Method Development
    作者:M. Jaoui、T. E. Kleindienst、M. Lewandowski、E. O. Edney
    DOI:10.1021/ac049919h
    日期:2004.8.1
    In this study, a new analytical technique was developed for the identification and quantification of multifunctional compounds containing simultaneously at least one hydroxyl or one carboxylic group, or both. This technique is based on derivatizing first the carboxylic group(s) of the multifunctional compound using an alcohol (e.g., methanol, 1-butanol) in the presence of a relatively strong Lewis acid (BF3) as a catalyst. This esterification reaction quickly and quantitatively converts carboxylic acids to their ester forms. The second step is based on silylation of the ester compounds using bis(trimethylsilyl) trifluoroacetamide (BSTFA) as the derivatizing agent. For compounds bearing ketone groups in addition to carboxylic and hydroxyl groups, a third step was used based on PFBHA derivatization of the carbonyls. Different parameters including temperature, reaction time, and effect due to artifacts were optimized. A GC/MS in EI and in methane-CI mode was used for the analysis of these compounds. The new approach was tested on a number of multifunctional compounds. The interpretation of their EI (70 eV) and CI mass spectra shows that critical information is gained leading to unambiguous identification of unknown compounds. For example, when derivatized only with BF3−methanol, their mass spectra comprise primary ions at m/z M•+ + 1, M•+ + 29, and M•+ − 31 for compounds bearing only carboxylic groups and M•+ + 1, M•+ + 29, M•+ − 31, and M+. − 17 for those bearing hydroxyl and carboxylic groups. However, when a second derivatization (BSTFA) was used, compounds bearing hydroxyl and carboxylic groups simultaneously show, in addition to the ions observed before, ions at m/z M•+ + 73, M•+ − 15, M•+ − 59, M•+ − 75, M•+ − 89, and 73. To the best of our knowledge, this technique describes systematically for the first time a method for identifying multifunctional oxygenated compounds containing simultaneously one or more hydroxyl and carboxylic acid groups.
    在本研究中,开发了一种新的分析技术,用于鉴定和定量含有至少一个羟基或一个羧基或两者的多官能团化合物。该技术基于首先使用醇(例如甲醇、1-丁醇)在相对较强的路易斯酸(BF3)催化下对多官能团化合物的羧基进行衍生化。这种酯化反应迅速且定量地将羧酸转化为酯形式。第二步是使用双(三甲基硅基)三氟乙酰胺(BSTFA)作为衍生化剂对酯化合物进行硅烷化。对于除羧基和羟基外还含有酮基的化合物,采用了基于PFBHA对羰基进行衍生化的第三步。优化了包括温度、反应时间和因人工产物引起的影响等多个参数。使用电子轰击源(EI)和甲烷化学电离(CI)模式的气相色谱/质谱法(GC/MS)分析了这些化合物。对多种多官能团化合物测试了新方法。对其EI(70 eV)和CI质谱的解释表明,获得了关键信息,从而能够明确鉴定未知化合物。例如,仅通过BF3−甲醇衍生化时,它们的质谱包含仅含有羧基的化合物的离子m/z M•+ + 1、M•+ + 29和M•+ − 31,以及同时含有羟基和羧基的化合物的离子m/z M•+ + 1、M•+ + 29、M•+ − 31和M•+ − 17。然而,当使用第二步衍生化(BSTFA)时,同时含有羟基和羧基的化合物除了之前观察到的离子外,还显示出m/z M•+ + 73、M•+ − 15、M•+ − 59、M•+ − 75、M•+ − 89和73的离子。据我们所知,这项技术首次系统地描述了一种鉴定同时含有一个或多个羟基和羧酸基团的多官能团含氧化合物的方法。
  • Alkane functionalization on a preparative scale by mercury-photosensitized cross-dehydrodimerization
    作者:Stephen H. Brown、Robert H. Crabtree
    DOI:10.1021/ja00190a032
    日期:1989.4
    5-trioxacyclohexane < ethanol < isobutane < THF < Etsub 3}SiH. The observed selectivities generally parallel those for homodimerization, reported in the preceding paper, but certain differences are noted, and reasons for the differences are proposed. The bond-dissociation energymore » of Etsub 3}SiH is estimated from the reactivity data to be 90 kcal/mol. Eleven new carbinols are synthesized. 39 refs., 6 tabs
    烷烃可以通过烷烃与醇、醚或硅烷之间的汞光敏反应以高转化率和高化学和量子产率在多克规模下官能化,得到同二聚体和交叉脱氢二聚体。由于同二聚体和交叉二聚体的极性差异很大,因此产物混合物的分离通常特别容易。当通过改变液体组成来调节气相中组分的比例时,也可以偏向产物组成。这对于最大化化学产率或通过有利于形成最容易分离的化合物对来简化分离是有用的。讨论了反应的机理基础,并详细描述了许多特定类型的合成,例如 2,2-二取代的甲醇。交叉二聚的选择性被证明超过了均二聚的选择性,并讨论了原因。不同化合物和化合物类别的相对反应性为 MeOH < 对二恶烷 < 环己烷 < 1,3,5-三恶六环己烷 < 乙醇 < 异丁烷 < THF < Etsub 3}SiH。观察到的选择性通常与前一篇论文中报道的均二聚化的选择性相似,但注意到了某些差异,并提出了差异的原因。Etsub 3}SiH 的键离解能根据反应性数据估计为
  • PROCESS FOR DOUBLE CARBONYLATION OF ALLYL ALCOHOLS TO CORRESPONDING DIESTERS
    申请人:EVONIK DEGUSSA GMBH
    公开号:US20170174610A1
    公开(公告)日:2017-06-22
    The invention relates to a process for doubly carbonylating allyl alcohols to the corresponding diesters, wherein a linear or branched allyl alcohol is reacted with a linear or branched alkanol (alcohol) with supply of CO and in the presence of a catalytic system composed of a palladium complex and at least one organic phosphorus ligand and in the presence of a hydrogen halide selected from HCl, HBr and HI.
    该发明涉及一种将烯丙醇双羰基化为相应的二酯的方法,其中线性或支链烯丙醇与线性或支链烷醇(醇)在供应CO的情况下与由钯配合物和至少一种有机磷配体组成的催化系统以及HCl、HBr和HI中选择的氢卤素的存在下反应。
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表征谱图

  • 氢谱
    1HNMR
  • 质谱
    MS
  • 碳谱
    13CNMR
  • 红外
    IR
  • 拉曼
    Raman
hnmr
mass
cnmr
ir
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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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