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1,3-dibenzylimidazolium | 94592-90-2

中文名称
——
中文别名
——
英文名称
1,3-dibenzylimidazolium
英文别名
1,3-Dibenzylimidazol-1-ium
1,3-dibenzylimidazolium化学式
CAS
94592-90-2
化学式
C17H17N2
mdl
——
分子量
249.335
InChiKey
AGKZPTNSLDZRHF-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):
    3.3
  • 重原子数:
    19
  • 可旋转键数:
    4
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.12
  • 拓扑面积:
    8.8
  • 氢给体数:
    0
  • 氢受体数:
    0

反应信息

  • 作为反应物:
    描述:
    1,3-dibenzylimidazoliumpentacarbonyl(1-methoxybenzylidene)chromium(0) 在 t-BuOK 作用下, 以 四氢呋喃 为溶剂, 以34%的产率得到
    参考文献:
    名称:
    以铬费休卡宾烯为羰基铬源合成N杂环卡宾铬配合物
    摘要:
    铬费歇尔卡宾络合物[Cr {OMe(R)}(CO)5 ]已被用作铬NHC络合物的合成中的羰基铬源。使用合成方法,可以合理的产率分离出各种NHC配体的铬配合物。此外,该方法可用于合成钼和钨NHC化合物。
    DOI:
    10.1016/j.jorganchem.2007.08.043
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文献信息

  • [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。
  • Iridium(I)-Catalyzed Alkylation Reactions To Form α-Alkylated Ketones
    作者:Sertaç Genç、Salih Günnaz、Bekir Çetinkaya、Süleyman Gülcemal、Derya Gülcemal
    DOI:10.1021/acs.joc.8b00043
    日期:2018.3.2
    α-alkylated ketones has been disclosed via the reaction of primary alcohols with secondary alcohols and ketones by using [IrCl(COD)(NHC)] complexes as a catalyst. Various α-alkylated ketones were obtained in high yields from the alkylation of alcohol with alcohol and ketone with alcohol through a borrowing hydrogen reaction by using 0.05–0.5 mol % iridium(I) and a catalytic amount of KOH (5–10 mol %)
    通过使用[IrCl(COD)(NHC)]络合物作为催化剂,通过伯醇与仲醇和酮的反应,已经公开了形成α-烷基化酮的高效且绿色的方法。通过使用0.05–0.5 mol%的(I)和催化量的KOH(5–10 mol%)通过借位氢反应,通过醇与醇的烷基化和酮与醇的酮的高收率获得各种α-烷基化的酮。在空气中并在很短的反应时间内作为碱。
  • [EN] DISSOLUTION OF CELLULOSE IN IONIC LIQUIDS<br/>[FR] DISSOLUTION DE CELLULOSE DANS DES LIQUIDES IONIQUES
    申请人:UNIV TEXAS TECH SYSTEM
    公开号:WO2019143802A1
    公开(公告)日:2019-07-25
    The present invention includes a method for dissolving cellulose comprising dissolving cellulose in an ionic liquid and a co-solvent, wherein the ionic liquid is an imidazolium-based ionic liquid with, e.g., a halide or acetate as the anion.
    该发明涉及一种溶解纤维素的方法,包括在一种离子液体和共溶剂中溶解纤维素,其中该离子液体是一种以咪唑为基础的离子液体,例如,卤化物或乙酸盐作为阴离子。
  • METHOD FOR THE PRODUCTION OF DISUBSTITUTED IMIDAZOLIUM SALTS
    申请人:Siemer Michael
    公开号:US20100249432A1
    公开(公告)日:2010-09-30
    Process for preparing 1,3-disubstituted imidazolium salts of the formula I where R1 and R3 are each, independently of one another, an organic radical having from 1 to 20 carbon atoms, R2, R4 and R5 are each, independently of one another, an H atom or an organic radical having from 1 to 20 carbon atoms, X is the anion of a hydrogen acid having a pK a of at least 2 (measured at 25° C., 1 bar in water or dimethyl sulfoxide) and n is 1, 2 or 3, wherein a) an α-dicarbonyl compound, an aldehyde, an amine and the hydrogen acid of the anion X − are reacted with one another and b) the reaction is carried out in water, a solvent which is miscible with water or a mixture thereof.
    制备1,3-二取代咪唑盐的公式I的过程,其中R1和R3分别独立地是具有1至20个碳原子的有机基团,R2、R4和R5分别独立地是一个氢原子或具有1至20个碳原子的有机基团,X是具有至少2的pKa(在25°C、1巴二甲基亚砜中测得)的氢酸根离子,n为1、2或3,其中a)α-二羰基化合物、醛、胺和阴离子X−的氢酸反应,b)反应在、与相溶的溶剂或二者的混合物中进行。
  • PLATINUM-N-HETEROCYCLIC CARBENE DERIVATIVES, PREPARATION THEREOF AND THERAPEUTIC USE THEREOF
    申请人:MAILLIET Patrick
    公开号:US20110172199A1
    公开(公告)日:2011-07-14
    The invention relates to the platinum N-heterocycle derivatives of general formula (I) in which—R 1 and/or R 2 are, independently of one another, an aryl or aralkyl group, each optionally substituted, a linear or branched C1-C6 alkyl group, a monocyclic C3-C7 cycloalkyl group or a linear or branched C2-C6 alkenyl group, or else R′ is a hydrogen atom and R is a group selected from the following groups: cycloalkyl or heterocycloalkyl, which is monocyclic or bicyclic and has from 3 to 8 carbon atoms, or benzyl, which is optionally substituted, or else R and R′ form, together with NH, a C3-C8 monocyclic or bicyclic heterocycloalkyl, V is a nitrogen atom or a C—R 4 radical, R 3 and/or R 4 are hydrogen or a phenyl group or R 3 and R 4 may also together form a C3-C6 alkylene radical or a C3-C6 heteroalkylene radical with one or more nitrogenous heteroatoms, it being possible for the carbon atoms of the heteroalkylene radical to be modified in the form of a carbonyl radical, and X is iodine, bromine, chlorine or a nitrato (—ONO 2 ) group.
    这项发明涉及通式(I)的N-杂环衍生物,其中-R1和/或R2分别是芳基或芳基烷基,每个都可以选择性地被取代,线性或支链的C1-C6烷基,单环C3-C7环烷基或线性或支链的C2-C6烯基,或者R′是氢原子,R是以下基团之一:单环或双环且具有3到8个碳原子的环烷基或杂环烷基,或者是可以选择性地被取代的苄基,或者R和R′与NH一起形成一个C3-C8单环或双环杂环烷基,V是氮原子或C—R4基团,R3和/或R4是氢或苯基,或者R3和R4也可以一起形成一个带有一个或多个含氮杂原子的C3-C6烷基或C3-C6杂烷基,杂烷基的碳原子可以以羰基基团的形式进行修饰,X是硝酸根(—ONO2)基团。
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