摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

α,α-bis(4-amino-3,5-dimethylphenyl)toluene | 258517-45-2

中文名称
——
中文别名
——
英文名称
α,α-bis(4-amino-3,5-dimethylphenyl)toluene
英文别名
4-[(4-Amino-3,5-dimethylphenyl)(phenyl)methyl]-2,6-dimethylaniline;4-[(4-amino-3,5-dimethylphenyl)-phenylmethyl]-2,6-dimethylaniline
α,α-bis(4-amino-3,5-dimethylphenyl)toluene化学式
CAS
258517-45-2
化学式
C23H26N2
mdl
MFCD00187206
分子量
330.473
InChiKey
MADRVTFUZLHYOU-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

  • 沸点:
    507.8±45.0 °C(Predicted)
  • 密度:
    1.093±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    5.4
  • 重原子数:
    25
  • 可旋转键数:
    3
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.22
  • 拓扑面积:
    52
  • 氢给体数:
    2
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    描述:
    α,α-bis(4-amino-3,5-dimethylphenyl)toluene硫酸三氧化硫 作用下, 反应 5.0h, 以91%的产率得到α,α-bis(4-amino-3,5-dimethylphenyl)-1-(3'-hydroxysulfonylphenyl)methane
    参考文献:
    名称:
    一种磺化芳香二胺化合物及其制备方法与应用
    摘要:
    本发明公开了一种磺化芳香二胺化合物及其制备方法与应用。磺化芳香二胺化合物如式I所示。式I所示磺化芳香二胺化合物的制备方法包括如下步骤:(1)在酸存在的条件下,式Ⅱ所示苯胺化合物与式Ⅲ所示苯甲醛化合物在水中进行反应;所述反应完毕后,用碱中和所述反应的体系,然后经重结晶得到式Ⅳ所示芳香二胺化合物;(2)在冰浴条件下,将式Ⅳ所示芳香二胺化合物加入至浓硫酸中,然后加入发烟硫酸进行反应,即得式I所示磺化芳香二胺化合物。本发明磺化芳香二胺化合物作为新型高效破乳剂和清水剂的核心引发剂或功能单体,在处理聚合物驱采出液方面具有重要的价值。
    公开号:
    CN103864648B
  • 作为产物:
    描述:
    苯甲醛2,6-二甲基苯胺盐酸 作用下, 以 四氢呋喃 为溶剂, 反应 25.0h, 以70%的产率得到α,α-bis(4-amino-3,5-dimethylphenyl)toluene
    参考文献:
    名称:
    大块α-二亚胺钯配合物负载氧化石墨烯作为铃木-宫浦反应的多相催化剂
    摘要:
    摘要 为了探索 Suzuki-Miyaura 反应的高效性,一种易于制备的带有空间体积大的 α-二亚胺的多相钯预催化剂共价负载在氧化石墨烯 (GO) 上。详细讨论了负载钯配合物的表征。描述了一种简单有效的 Pd 催化交叉偶联方案,表明庞大的 α-二亚胺配体对于促进 CAr-CAr 转化至关重要。这种固定化系统提供了一种直接访问范围广泛的具有优异官能团耐受性的芳基溴化物。
    DOI:
    10.1016/j.molstruc.2020.128537
点击查看最新优质反应信息

文献信息

  • [EN] TRANSITION METAL COMPOUNDS FOR OLEFIN POLYMERIZATION AND OLIGOMERIZATION<br/>[FR] COMPOSES METALLIQUES DE TRANSITION POUR LA POLYMERISATION D'OLEFINES ET L'OLIGOMERISATION
    申请人:EXXONMOBIL CHEM PATENTS INC
    公开号:WO2005118605A1
    公开(公告)日:2005-12-15
    This invention relates to new transition metal catalyst compounds represented by the formula (I): where: M and M' are, independently, a group 8, 9, 10 or 11 transition metal, preferably Ni, Co, Pd, Cu or Fe; each R group is, independently, is, hydrogen, or a hydrocarbyl, substituted hydrocarbyl, halocarbyl, substituted halocarbyl, silylcarbyl, substituted silylcarbyl, germylcarbyl, or substituted germylcarbyl substituents, and optionally, adjacent R groups may join together to form a substituted or unsubstituted, saturated, partially unsaturated, or aromatic cyclic or polycyclic substituent; R' is hydrogen, or a hydrocarbyl, substituted hydrocarbyl, halocarbyl, substituted halocarbyl, silylcarbyl, substituted silylcarbyl, germylcarbyl, or substituted germylcarbyl substituents, and optionally, adjacent R groups may join together with R' to form a substituted or unsubstituted, saturated, partially unsaturated, or aromatic cyclic or polycyclic substituent; each X group is, independently, is, hydrogen, a halogen, or a hydrocarbyl, substituted hydrocarbyl, halocarbyl, substituted halocarbyl, silylcarbyl, substituted sililcarbyl, germylcarbyl, or substituted germylcarbyl substituents, and optionally, adjacent X groups may join together to form a substituted or unsubstituted, saturated, partially unsaturated, or aromatic cyclic or polycyclic substituent; m and m’ are, independently, 0, 1, 2, or 3; z and z’ are, independently, 0, 1, 2, or 3; N is nitrogen; Q is hydrogen, or a hydrocarbyl, substituted hydrocarbyl, halocarbyl, substituted halocarbyl, silylcarbyl, substituted silylcarbyl, germylcarbyl, or substituted germylcarbyl substituents; Q’ is hydrogen, or a hydrocarbyl, substituted hydrocarbyl, halocarbyl, substituted halocarbyl, silylcarbyl, substituted silylcarbyl, germylcarbyl or substituted germylcarbyl substituents; and L is a hydrocarbyl, substituted hydrocarbyl, halocarbyl, substituted halocarbyl, silylcarbyl, substituted silylcarbyl, germylcarbyl, or substituted germylcarbyl substituent.
    这项发明涉及由式(I)表示的新过渡金属催化剂化合物,其中:M和M'分别是8、9、10或11族过渡金属,优选为Ni、Co、Pd、Cu或Fe;每个R基分别是氢,或烃基,取代烃基,卤代烃基,取代卤代烃基,硅烃基,取代硅烃基,锗烃基,或取代锗烃基取代基,且可选地,相邻的R基可以结合在一起形成取代或未取代的饱和、部分不饱和或芳香环或多环取代基;R'是氢,或烃基,取代烃基,卤代烃基,取代卤代烃基,硅烃基,取代硅烃基,锗烃基,或取代锗烃基取代基,且可选地,相邻的R基可以与R'结合在一起形成取代或未取代的饱和、部分不饱和或芳香环或多环取代基;每个X基分别是氢,卤素,或烃基,取代烃基,卤代烃基,取代卤代烃基,硅烃基,取代硅烃基,锗烃基,或取代锗烃基取代基,且可选地,相邻的X基可以结合在一起形成取代或未取代的饱和、部分不饱和或芳香环或多环取代基;m和m'分别为0、1、2或3;z和z'分别为0、1、2或3;N为氮;Q为氢,或烃基,取代烃基,卤代烃基,取代卤代烃基,硅烃基,取代硅烃基,锗烃基,或取代锗烃基取代基;Q'为氢,或烃基,取代烃基,卤代烃基,取代卤代烃基,硅烃基,取代硅烃基,锗烃基,或取代锗烃基取代基;L为烃基,取代烃基,卤代烃基,取代卤代烃基,硅烃基,取代硅烃基,锗烃基,或取代锗烃基取代基。
  • Synthesis and monolayer behaviors of optically active 1,12- dimethylbenzo[c]phenanthrene-5,8-diamides and the formation of chiral langmuir-blodgett films
    作者:Hitoshi Okubo、Fei Feng、Daisuke Nakano、Tomokazu Hirata、Masahiko Yamaguchi、Tokuji Miyashita
    DOI:10.1016/s0040-4020(99)00969-2
    日期:1999.12
    previously reported that an optically active cyclic amide consisting of a helical chiral 1,12-dimethylbenzo[c]phenanthrene-5, 8-dicarboxylic acid forms a stable monolayer on the water surface, and that the monolayer can be transferred on a solid support giving optically active Langmuir-Blodgett (LB) films. In this study, several related amides were synthesized, and their monolayer behaviors were investigated
    我们以前曾报道过,由螺旋手性1,12-二甲基苯并[ c ]菲-5,8-二羧酸组成的旋光环状酰胺在水表面形成稳定的单层,并且该单层可以转移到固体载体上得到光学活性的朗缪尔-布洛杰特(LB)膜。在这项研究中,合成了几种相关的酰胺,并对其单层行为进行了研究,以期制备具有官能团的光学活性LB膜。结果表明,环状酰胺结构和环己基部分对于在水表面形成稳定的单分子层至关重要。仲酰胺的N-烷基化不会严重影响单层的形成,而手性LB膜可通过N,N获得环酰胺的-双(3-巯基丙基)衍生物。
  • NOVEL (POLY)AMINE COMPOUND, RESIN AND CURED PRODUCT
    申请人:Mitsubishi Gas Chemical Company, Inc.
    公开号:US20200172470A1
    公开(公告)日:2020-06-04
    A (poly)amine compound represented by the following formula (0): wherein R X is a 2n A -valent group having 1 to 70 carbon atoms or a single bond; each R 1A is independently any of an alkyl group having 1 to 30 carbon atoms and optionally having a substituent, an aryl group having 6 to 30 carbon atoms and optionally having a substituent, a crosslinking group having 2 to 30 carbon atoms and optionally having a substituent, an alkoxy group having 1 to 30 carbon atoms and optionally having a substituent, a halogen atom, a nitro group, an amino group having 0 to 30 carbon atoms and optionally having a substituent, a carboxyl group, a thiol group and a hydroxy group, wherein when R 1A is any of the alkyl group, the aryl group, the crosslinking group and the alkoxy group, R 1A optionally contains at least one bond selected from the group consisting of an ether bond, a ketone bond and an ester bond, and at least one R 1A is an amino group having 0 to 30 carbon atoms and optionally having a substituent; X is an oxygen atom or a sulfur atom, or X is optionally absent; each R independently represents any of a benzene ring, a biphenyl ring, a naphthalene ring, an anthracene ring and a pyrene ring; each m is independently an integer of 0 to 9, wherein at least one m is an integer of 1 to 9; and n A is an integer of 1 to 4.
    由以下公式(0)表示的(聚)胺化合物:其中RX是一个具有1到70个碳原子或单键的2nA价基团;每个R1A独立地是1到30个碳原子的烷基基团,可选地具有取代基,含有6到30个碳原子的芳基基团,可选地具有取代基,含有2到30个碳原子的交联基团,可选地具有取代基,含有1到30个碳原子的烷氧基团,可选地具有取代基,卤原子,硝基基团,含有0到30个碳原子的氨基基团,可选地具有取代基,羧基,硫醇基和羟基,其中当R1A是烷基基团、芳基基团、交联基团和烷氧基团中的任意一种时,R1A可选地含有至少一种从醚键、酮键和酯键组成的键,至少有一个R1A是含有0到30个碳原子且可选地具有取代基的氨基基团;X是氧原子或硫原子,或X可选地不存在;每个R独立地代表苯环、联苯环、萘环、蒽环和芘环中的任意一种;每个m独立地是0到9的整数,至少有一个m是1到9的整数;nA是1到4的整数。
  • Organic compounds
    申请人:Clariant International Ltd.
    公开号:EP2251383A1
    公开(公告)日:2010-11-17
    Compounds of the general formula (I) a process for their preparation and their use for dyeing and/or printing organic substrates.
    通式(I)的化合物的制备方法及其用于有机基质染色和/或印花的用途。
  • Transition Metal Compounds for Olefin Polymerization and Oligomerization
    申请人:Solan A. Gregory
    公开号:US20080033125A1
    公开(公告)日:2008-02-07
    This invention relates to new transition metal catalyst compounds represented by the formula (I): where: M and M′ are, independently, a group 8, 9, 10 or 11 transition metal, preferably Ni, Co, Pd, Cu or Fe; each R group is, independently, is, hydrogen, or a hydrocarbyl, substituted hydrocarbyl, halocarbyl, substituted halocarbyl, silylcarbyl, substituted silylcarbyl, germylcarbyl, or substituted germylcarbyl substituents, and optionally, adjacent R groups may join together to form a substituted or unsubstituted, saturated, partially unsaturated, or aromatic cyclic or polycyclic substituent; R′ is hydrogen, or a hydrocarbyl, substituted hydrocarbyl, halocarbyl, substituted halocarbyl, silylcarbyl, substituted silylcarbyl, germylcarbyl, or substituted germylcarbyl substituents, and optionally, adjacent R groups may join together with R′ to form a substituted or unsubstituted, saturated, partially unsaturated, or aromatic cyclic or polycyclic substituent; each X group is, independently, is, hydrogen, a halogen, or a hydrocarbyl, substituted hydrocarbyl, halocarbyl, substituted halocarbyl, silylcarbyl, substituted silylcarbyl, germylcarbyl, or substituted germylcarbyl substituents, and optionally, adjacent X groups may join together to form a substituted or unsubstituted, saturated, partially unsaturated, or aromatic cyclic or polycyclic substituent; m and m′ are, independently, 0, 1, 2, or 3; z and z′ are, independently, 0, 1, 2, or 3; N is nitrogen; Q is hydrogen, or a hydrocarbyl, substituted hydrocarbyl, halocarbyl, substituted halocarbyl, silylcarbyl, substituted silylcarbyl, germylcarbyl, or substituted germylcarbyl substituents; Q′ is hydrogen, or a hydrocarbyl, substituted hydrocarbyl, halocarbyl; substituted halocarbyl, silylcarbyl, substituted silylcarbyl, germylcarbyl, or substituted germylcarbyl substituents; and L is a hydrocarbyl, substituted hydrocarbyl, halocarbyl, substituted halocarbyl, silylcarbyl, substituted silylcarbyl, germylcarbyl, or substituted germylcarbyl substituent.
    本发明涉及由公式(I)表示的新过渡金属催化剂化合物:其中:M和M'分别是8、9、10或11族过渡金属,优选为Ni、Co、Pd、Cu或Fe;每个R基团独立地是氢或烃基、取代烃基、卤代烃基、取代卤代烃基、硅基烃基、取代硅基烃基、锗基烃基或取代锗基烃基取代基,并且选择性地,相邻的R基团可以结合在一起形成取代或未取代的饱和、部分不饱和或芳香族或多环取代基;R'是氢或烃基、取代烃基、卤代烃基、取代卤代烃基、硅基烃基、取代硅基烃基、锗基烃基或取代锗基烃基取代基,并且选择性地,相邻的R基团可以与R'结合在一起形成取代或未取代的饱和、部分不饱和或芳香族或多环取代基;每个X基团独立地是氢、卤素或烃基、取代烃基、卤代烃基、取代卤代烃基、硅基烃基、取代硅基烃基、锗基烃基或取代锗基烃基取代基,并且选择性地,相邻的X基团可以结合在一起形成取代或未取代的饱和、部分不饱和或芳香族或多环取代基;m和m'独立地为0、1、2或3;z和z'独立地为0、1、2或3;N为氮;Q为氢或烃基、取代烃基、卤代烃基、取代卤代烃基、硅基烃基、取代硅基烃基、锗基烃基或取代锗基烃基取代基;Q'为氢或烃基、取代烃基、卤代烃基、取代卤代烃基、硅基烃基、取代硅基烃基、锗基烃基或取代锗基烃基取代基;以及L为烃基、取代烃基、卤代烃基、取代卤代烃基、硅基烃基、取代硅基烃基、锗基烃基或取代锗基烃基取代基。
查看更多

同类化合物

(3-三苯基甲氨基甲基)吡啶 非马沙坦杂质1 隐色甲紫-d6 隐色孔雀绿-d6 隐色孔雀绿 隐色乙基结晶紫 降钙素杂质10 酸性黄117 酸性蓝119 酚酞啉 酚酞二硫酸钾水合物 萘,1-甲氧基-3-甲基 苯酚,4-(1,1-二苯基丙基)- 苯甲醇,4-溴-a-(4-溴苯基)-a-苯基- 苯甲酸,4-(羟基二苯甲基)-,甲基酯 苯甲基N-[(2(三苯代甲基四唑-5-基-1,1联苯基-4-基]-甲基-2-氨基-3-甲基丁酸酯 苯基双-(对二乙氨基苯)甲烷 苯基二甲苯基甲烷 苯基二[2-甲基-4-(二乙基氨基)苯基]甲烷 苯基{二[4-(三氟甲基)苯基]}甲醇 苯基-二(2-羟基-5-氯苯基)甲烷 苄基2,3,4-三-O-苄基-6-O-三苯甲基-BETA-D-吡喃葡萄糖苷 苄基 5-氨基-5-脱氧-2,3-O-异亚丙基-6-O-三苯甲基呋喃己糖苷 苄基 2-乙酰氨基-2-脱氧-6-O-三苯基-甲基-alpha-D-吡喃葡萄糖苷 苄基 2,3-O-异亚丙基-6-三苯甲基-alpha-D-甘露呋喃糖 膦酸,1,2-乙二基二(磷羧基甲基)亚氨基-3,1-丙二基次氮基<三价氮基>二(亚甲基)四-,盐钠 脱氢奥美沙坦-2三苯甲基奥美沙坦脂 美托咪定杂质28 绿茶提取物茶多酚陕西龙孚 结晶紫 磷,三(4-甲氧苯基)甲基-,碘化 碱性蓝 硫代硫酸氢 S-[2-[(3,3,3-三苯基丙基)氨基]乙基]酯 盐酸三苯甲基肼 白孔雀石绿-d5 甲酮,(反-4-氨基-4-甲基环己基)-4-吗啉基- 甲基三苯基甲基醚 甲基6-O-(三苯基甲基)-ALPHA-D-吡喃甘露糖苷三苯甲酸酯 甲基3,4-O-异亚丙基-2-O-甲基-6-O-三苯甲基吡喃己糖苷 甲基2-甲基-N-{[4-(三氟甲基)苯基]氨基甲酰}丙氨酸酸酯 甲基2,3,4-三-O-苯甲酰基-6-O-三苯甲基-ALPHA-D-吡喃葡萄糖苷 甲基2,3,4-三-O-苄基-6-O-三苯甲基-ALPHA-D-吡喃葡萄糖苷 甲基2,3,4-三-O-(苯基甲基)-6-O-(三苯基甲基)-ALPHA-D-吡喃半乳糖苷 甲基-6-O-三苯基甲基-alpha-D-吡喃葡萄糖苷 甲基(1-trityl-1H-imidazol-4-yl)乙酸酯 甲基 2,3,4-三-O-苄基-6-O-三苯基甲基-ALPHA-D-吡喃甘露糖苷 环丙胺,1-(1-甲基-1-丙烯-1-基)- 溶剂紫9 溴化N,N,N-三乙基-2-(三苯代甲基氧代)乙铵 海涛林