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1-butyl 3-methyl-imidazole | 120624-79-5

中文名称
——
中文别名
——
英文名称
1-butyl 3-methyl-imidazole
英文别名
butaneyl-3-methylimidazole;butyl-3-methylimidazole;1-Methyl-2-butylimidazole;2-butyl-1-methylimidazole
1-butyl 3-methyl-imidazole化学式
CAS
120624-79-5
化学式
C8H14N2
mdl
——
分子量
138.213
InChiKey
HGGLDADJQQPKKC-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):
    1.7
  • 重原子数:
    10
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.62
  • 拓扑面积:
    17.8
  • 氢给体数:
    0
  • 氢受体数:
    1

反应信息

  • 作为反应物:
    描述:
    1-溴辛烷1-butyl 3-methyl-imidazole四氢呋喃 为溶剂, 反应 24.0h, 生成
    参考文献:
    名称:
    铌(v)和氯化咪唑鎓溴化物作为二氧化碳和环氧丙烷的环加成高效的双催化剂体系†
    摘要:
    据报道,氯化铌(V)和几种咪唑鎓溴化物作为催化剂将环氧丙烷(PO)与二氧化碳环加成成碳酸亚丙酯(PC)。合成了31种不同的咪唑鎓溴化物,它们在所有5个咪唑鎓环原子上都有不同的取代基,其中17种以前从未报道过。研究了咪唑环上不同取代方式(空间和电子变化以及在PO中的溶解度)对催化活性的影响。催化剂结构的优化允许在温和的反应条件下以高的反应速率以非常好的收率和对PC的选择性来平衡二氧化碳的价位。
    DOI:
    10.1039/c3cy01057k
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文献信息

  • Method of preparation of halogen-free ionic liquids and ionic liquids prepared in this manner
    申请人:Cassol Claudia Cristiana
    公开号:US20080045723A1
    公开(公告)日:2008-02-21
    The reaction of N-alkylimidazol with alkyl sulfonates, at room temperature, favors the production of 1,3-dialkylimidazolium alkane-sulfonates as crystalline solids at high yields. The alkane-sulfonate anions may be easily substituted by a series of other anions [BF 4 , PF 6 , PF 3 (CF 2 CF 3 ) 3 , CF 3 SO 3 and (CF 3 SO 2 ) 2 N] through simple anion, salt, or acid reactions in water at room temperature. The extraction with dichloromethane, filtration, and evaporation of the solvent, allows the production of the desired ionic liquids at a yield of 80-95%. The purity of these ionic liquids (in some cases >99.4%) is performed using the intensity of 13 C satellite signals from the magnetic resonance spectrums of the N-methyl imidazolium group as an internal standard.
    N-烷基咪唑与烷基磺酸盐在室温下反应,有利于高产率地生成1,3-二烷基咪唑磺酸盐作为结晶固体。烷磺酸盐阴离子可以通过简单的阴离子、盐或酸反应在室温下在中轻松被一系列其他阴离子[BF 4 , PF 6 , PF 3 (CF 2 CF 3 ) 3 , CF 3 SO 3 和(CF 3 SO 2 ) 2 N]所取代。用二氯甲烷萃取、过滤和溶剂蒸发,可以以80-95%的产率生产所需的离子液体。这些离子液体的纯度(在某些情况下>99.4%)是通过使用N-甲基咪唑基团的 13 C卫星信号强度作为内部标准来进行的。
  • [EN] IONIC LIQUID SOLVENTS<br/>[FR] SOLVANTS LIQUIDES IONIQUES
    申请人:UNIV DUBLIN CITY
    公开号:WO2010097412A1
    公开(公告)日:2010-09-02
    A chiral ionic compound comprising an alkyl substituted imidazolium or pyridinium cationic core having an alkyl ester side chain (-alkyl-C(O)O-) directly linked to the core and an associated counter anion, characterized in that the -O- atom of the ester side chain is linked to an alpha, a beta or a gamma hydroxycarboxylic acid functionality via the alpha, beta or gamma hydroxy of the acid functionality and the hydroxycarboxylic acid functionality has at least one asymmetric carbon, or characterized in that an -N= atom of the alkyl substituted imidazolium or pyridinium cationic core is substituted with an alpha, a beta or a gamma hydroxy group of a alpha, a beta or a gamma hydroxycarboxylic acid functionality and the hydroxycarboxylic acid functionality has at least one asymmetric carbon. The chiral ionic liquids (CILs) may be used as novel solvents, in particular for organic synthesis. The CILs have the potential to induce asymmetry into substrates or catalysts in a variety of organic transformations. A number of the compounds have low antimicrobial and low antifungal toxicities and are also biodegradable CILs.
    一种手性离子化合物,包括具有烷基取代的咪唑吡啶阳离子核心,其具有直接连接到核心的烷基酯侧链(-烷基-C(O)O-)和相关的对应阴离子,其特征在于酯侧链的-O-原子通过α、β或γ羟基羧酸功能与羧酸功能的α、β或γ羟基相连,且羟基羧酸功能具有至少一个不对称碳,或者其特征在于烷基取代的咪唑吡啶阳离子核心的-N=原子被α、β或γ羟基羧酸功能的α、β或γ羟基取代,且羟基羧酸功能具有至少一个不对称碳。这种手性离子液体(CILs)可用作新型溶剂,特别适用于有机合成。这些CILs有潜力在各种有机转化中向底物或催化剂引入不对称性。其中一些化合物具有低抗菌和低抗真菌毒性,并且也是可生物降解的CILs。
  • [EN] BIODEGRADABLE SOLVENTS FOR THE CHEMICAL INDUSTRY<br/>[FR] SOLVANTS BIODÉGRADABLES POUR L'INDUSTRIE CHIMIQUE
    申请人:UNIV DUBLIN CITY
    公开号:WO2009024607A1
    公开(公告)日:2009-02-26
    This invention relates to ionic liquid (ILs) solvents for chemical synthesis based on an alkyl - imidazolium cation core containing ionic liquids which have enhanced biodegradability and reduced toxicity relative to existing imidazolium bases ILs such as 1-butyl-3-methylimidazolium (bmmim) salts. Many of the described ILs produce a score of over 60% biodegradability over 28 days in a biodegradability test such as the Sturm Test, the Closed Bottle Test (OECD 301D) or the CO2 Headspace Test (ISO 14593). The ILs of the invention comprise an alkyl substituted imidazolium cationic core having a -C=OX- side chain in the 3-position of the imidazole ring, wherein X = O, NH, N or S and an associated counteranion characterized in that the -C=OX side chain comprises at least one ether linkage. The biodegradable and non-toxic IL may be used as green solvents for the chemical, pharmaceutical, biofuel and biomass industries. The ILs of the invention are particularly useful in hydrogenation, pericyclic and metathesis reactions.
    这项发明涉及一种基于含有烷基-咪唑啉阳离子核心的离子液体溶剂,用于化学合成,这些离子液体相对于现有如1-丁基-3-甲基咪唑啉(bmmim)盐类的咪唑啉离子液体,具有增强的生物降解性和降低的毒性。所描述的许多离子液体生物降解性测试中,例如Sturm测试、封闭瓶测试(OECD 301D)或CO2顶空测试(ISO 14593)中,28天内生物降解率超过60%。本发明的离子液体包括一个在咪唑啉环的3位上带有-C=OX-侧链的烷基取代咪唑啉阳离子核心,其中X=O,NH,N或S,以及一个相关的反离子,其特征在于-C=OX侧链至少包含一个醚键。这些生物降解且无毒的离子液体可作为化学、制药、生物燃料和生物质工业的绿色溶剂。特别是,本发明的离子液体在氢化、周环和复分解反应中非常有用。
  • [EN] COMBINATION OF CB2 MODULATORS AND PDE4 INHIBITORS FOR USE IN MEDICINE<br/>[FR] COMBINAISON DE MODULATEURS DU CB2 ET D'INHIBITEURS DE LA PDE4 UTILISEE EN MEDECINE
    申请人:GLAXO GROUP LTD
    公开号:WO2005074939A1
    公开(公告)日:2005-08-18
    Combination of one or more CB2 modulators such as a compound of formula (I), (II) and (III); and one more PDE4 inhibitors are useful of treating conditions which are mediated by the activity of CB2 receptors or conditions which are mediated by PDE4, such as an immune disorder, an inflamatory disorder, pain, rheumatoid.
    一种或多种CB2调节剂的组合,例如式(I)、(II)和(III)的化合物;以及一种或多种PDE4抑制剂对于治疗由CB2受体活性介导的疾病或由PDE4介导的疾病,如免疫紊乱、炎症性疾病、疼痛、类风湿等症状是有用的。
  • [EN] METHOD FOR TREATING FIBROSIS AND CANCER WITH IMIDAZOLIUM AND IMIDAZOLINIUM COMPOUNDS<br/>[FR] PROCÉDÉ DE TRAITEMENT DE LA FIBROSE ET DU CANCER AVEC DE L'IMIDAZOLIUM ET DES COMPOSÉS À BASE D'IMIDAZOLINIUM
    申请人:AGENCY SCIENCE TECH & RES
    公开号:WO2009096905A1
    公开(公告)日:2009-08-06
    There is presently provided methods for delivering an anti-fibrotic or anti-cancer agent to a cell. The methods comprise contacting a cell with an effective amount of imidazolium and imidazolinium compounds as described herein, including imidazolium and imidazolinium salts.
    目前提供了一种将抗纤维化或抗癌药物输送到细胞的方法。该方法包括将细胞与本文所述的咪唑咪唑啉化合物的有效量接触,包括咪唑咪唑啉盐。
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