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2,6-二氨基-3,5-二乙基甲苯 | 2095-01-4

中文名称
2,6-二氨基-3,5-二乙基甲苯
中文别名
——
英文名称
2-methyl-4,6-diethylphenylene-1,3-diamine
英文别名
3,5-diethyltoluene-2,6-diamine;2,6-diamino-3,5-diethyltoluene;4,6-diethyl-2-methyl-m-phenylenediamine;4,6-Diaethyl-2-methyl-m-phenylendiamin;1-methyl-3,5-diethyl-2,6-phenylenediamine;2-methyl-4,6-diethyl-1,3-phenylenediamine;1,3-Benzenediamine, 4,6-diethyl-2-methyl-;4,6-diethyl-2-methylbenzene-1,3-diamine
2,6-二氨基-3,5-二乙基甲苯化学式
CAS
2095-01-4
化学式
C11H18N2
mdl
——
分子量
178.277
InChiKey
RQEOBXYYEPMCPJ-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:
    58 °C
  • 沸点:
    152-155 °C(Press: 5 Torr)
  • 密度:
    1.013±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.5
  • 重原子数:
    13
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.45
  • 拓扑面积:
    52
  • 氢给体数:
    2
  • 氢受体数:
    2

安全信息

  • 海关编码:
    2921519090
  • 储存条件:
    2-8℃

SDS

SDS:1e11984b97c6f6aef64b8323c0ef1ed0
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上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

点击查看最新优质反应信息

文献信息

  • [EN] METHOD OF PURIFYING DIANHYDRIDES, THE DIANHYDRIDES FORMED THEREBY, AND POLYETHERIMIDES FORMED THEREFROM<br/>[FR] PROCÉDÉ DE PURIFICATION DES DIANHYDRIDES, DIANHYDRIDES AINSI OBTENUS, ET POLYÉTHERIMIDES FORMÉS À PARTIR DE CEUX-CI
    申请人:SABIC INNOVATIVE PLASTICS IP
    公开号:WO2009120212A1
    公开(公告)日:2009-10-01
    A method for purifying an oxydiphthalic anhydride comprises diluting a first mixture comprising an oxydiphthalic anhydride, a solvent, a catalyst, and an inorganic salt with a solvent, to provide a second mixture having a solids content of 10 to 30 percent based on total weight of the second mixture; filtering and washing the solids of the second mixture at a temperature below the crystallization point temperature of the oxydiphthalic anhydride to provide a third mixture; hydrolyzing the third mixture by adding water and a water-soluble acid to form a fourth mixture; heating the fourth mixture; then cooling to provide a solid-liquid mixture, optionally decanting a portion of the liquid, re diluting the remaining solid-liquid mixture, then filtering to provide a solid component; washing the solid component with water to provide a fifth mixture of oxydiphthalic tetra acid and water; ring closing the oxydiphthalic tetra acid to provide oxydiphthalic anhydride, and filtering the oxydiphthalic anhydride.
    一种用于纯化氧二苯二甲酸酐的方法包括将含有氧二苯二甲酸酐、溶剂、催化剂和无机盐的第一混合物稀释至含固体物含量为总重量的10至30%的第二混合物;在低于氧二苯二甲酸酐的结晶点温度的温度下过滤和洗涤第二混合物的固体以提供第三混合物;通过加入水和水溶性酸水解第三混合物以形成第四混合物;加热第四混合物;然后冷却以提供固液混合物,可选择性地倾倒部分液体,重新稀释剩余的固液混合物,然后过滤以提供固体组分;用水洗涤固体组分以提供氧二苯四甲酸和水的第五混合物;闭环氧二苯四甲酸以提供氧二苯二甲酸酐,并过滤氧二苯二甲酸酐。
  • Diimines and secondary diamines
    申请人:Lee Y. John
    公开号:US20060217567A1
    公开(公告)日:2006-09-28
    This invention provides aromatic diimines which have imino hydrocarbylidene groups with at least two carbon atoms, and aromatic secondary diamines which have amino hydrocarbyl groups with at least two carbon atoms. Both the aromatic diimines and the aromatic secondary diamines either are in the form of one phenyl ring, or are in the form of two phenyl rings connected by an alkylene bridge; each position ortho to an imino group or an amino group bears a hydrocarbyl group. When in the form of one phenyl ring, there are two imino groups on the ring or two amino groups on the ring; the imino groups or amino groups are meta or para relative to each other. When in the form of two phenyl rings connected by an alkylene bridge, there is either one imino group or one amino group on each phenyl ring. Also provided are processes for forming diimines and secondary diamines.
    这项发明提供了具有至少两个碳原子的亚烷基亚胺基团的芳香二亚胺和具有至少两个碳原子的氨基亚烷基团的芳香二胺。这些芳香二亚胺和芳香二胺可以是一个苯环的形式,也可以是由烷基桥连接的两个苯环的形式;每个邻位对着亚烷基基团或氨基基团。当以一个苯环的形式时,环上有两个亚胺基团或两个氨基团;亚胺基团或氨基团互为间位或对位。当以由烷基桥连接的两个苯环的形式时,每个苯环上要么有一个亚胺基团,要么有一个氨基基团。还提供了形成二亚胺和二胺的方法。
  • Method of Purifying Dianhydrides, the Dianhydrides Formed Thereby, and Polyetherimides Formed Therefrom
    申请人:Bernabe Beatriz Penalver
    公开号:US20090247727A1
    公开(公告)日:2009-10-01
    A method for purifying an oxydiphthalic anhydride comprises diluting a first mixture comprising an oxydiphthalic anhydride, a solvent, a catalyst, and an inorganic salt with a solvent, to provide a second mixture having a solids content of 10 to 30 percent based on total weight of the second mixture; filtering and washing the solids of the second mixture at a temperature below the crystallization point temperature of the oxydiphthalic anhydride to provide a third mixture; hydrolyzing the third mixture by adding water and a water-soluble acid to form a fourth mixture; heating the fourth mixture; then cooling to provide a solid-liquid mixture, optionally decanting a portion of the liquid, rediluting the remaining solid-liquid mixture, then filtering to provide a solid component; washing the solid component with water to provide a fifth mixture of oxydiphthalic tetraacid and water; ring closing the oxydiphthalic tetraacid to provide oxydiphthalic anhydride, and filtering the oxydiphthalic anhydride.
    一种纯化氧二苯甲酸酐的方法包括将包含氧二苯甲酸酐、溶剂、催化剂和无机盐的第一混合物稀释至含固体物含量为总重量的10至30%的第二混合物;在低于氧二苯甲酸酐结晶点温度的温度下过滤和洗涤第二混合物的固体,得到第三混合物;通过加入水和水溶性酸水解第三混合物以形成第四混合物;加热第四混合物;然后冷却以得到固液混合物,可选择性地倾倒一部分液体,重新稀释剩余的固液混合物,然后过滤以得到固体成分;用水洗涤固体成分以提供氧二苯甲酸四酸和水的第五混合物;将氧二苯甲酸四酸环合以提供氧二苯甲酸酐,并过滤氧二苯甲酸酐。
  • Method of purifying dianhydrides
    申请人:Pressman James Eric
    公开号:US20070117990A1
    公开(公告)日:2007-05-24
    Disclosed herein is a method for purification of dianhydrides comprising a substantial amount (10000 ppm or more) of at least one metal salt. In one aspect the method is useful for the purification of dianhydrides prepared by the reaction of a halophthalic anhydride with a metal carbonate and may be optionally catalyzed by a phase transfer catalyst. The purification of the dianhydrides may be accomplished by hydrolyzing the dianhydride metal salt mixture directly to a tetraacid with an inorganic acid, followed by separating the impurities from an aqueous phase, and subsequently heating the tetraacid to effect ring closure to form a purified dianhydride having less than 50 parts per million metal halide and lower levels of other residual impurities. In one aspect the method is highly effective in removing phase transfer catalyst impurities such as hexalkylguanidinium halides initially present in the dianhydride undergoing purification.
    本文揭示了一种用于纯化含有大量(10000 ppm或更多)至少一种金属盐的二酐的方法。在一个方面,该方法适用于通过卤酸酐与金属碳酸盐反应制备的二酐的纯化,并且可以选择性地由相转移催化剂催化。通过将二酐金属盐混合物直接水解为四羧酸,随后从水相中分离杂质,并随后加热四羧酸以实现环闭合形成纯化的二酐,其中金属卤化物含量低于50ppm,其他残留杂质水平也较低。在一个方面,该方法在去除最初存在于正在纯化的二酐中的相转移催化剂杂质(如己烷基胍盐)方面非常有效。
  • COMPOSITIONS AND METHODS FOR POLYMER COMPOSITES
    申请人:Chan Pong Kwok
    公开号:US20080021175A1
    公开(公告)日:2008-01-24
    This invention relates to organic salt compositions useful in the preparation of organoclay compositions, polymer-organoclay composite compositions, and methods for the preparation of polymer nanocomposites. In one embodiment, the present invention provides a pyridinium salt having structure XV wherein Ar 6 , Ar 7 , and Ar 8 are independently C 2 -C 50 aromatic radicals; “b” is a number from 0 to 2; “d” is a number from 0 to 4; R 3 and R 4 are independently at each occurrence a halogen atom, a C 1 -C 20 aliphatic radical, a C 5 -C 20 cycloaliphatic radical, or a C 2 -C 20 aromatic radical; Z is a bond, a divalent C 1 -C 20 aliphatic radical, a divalent C 5 -C 20 cycloaliphatic radical, a divalent C 2 -C 20 aromatic radical, an oxygen linking group, a sulfur linking group, a SO 2 linking group, or a Se linking group; Ar 9 is a C 10 -C 200 aromatic radical, or a polymer chain comprising at least one aromatic group; and X − is a charge balancing counterion.
    这项发明涉及有机盐组合物,用于制备有机粘土组合物、聚合物-有机粘土复合物组合物,以及制备聚合物纳米复合材料的方法。在一个实施例中,本发明提供了一种具有结构XV的吡啶盐,其中Ar6、Ar7和Ar8分别是C2-C50芳香基团;“b”是从0到2的数字;“d”是从0到4的数字;R3和R4在每次出现时独立地是卤素原子、C1-C20脂肪基、C5-C20环脂肪基或C2-C20芳香基;Z是一个键合、二价的C1-C20脂肪基、二价的C5-C20环脂肪基、二价的C2-C20芳香基、氧链连接基、硫链连接基、SO2链连接基或Se链连接基;Ar9是一个C10-C200芳香基团,或者包含至少一个芳香基团的聚合物链;X^−是一个电荷平衡的对离子。
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同类化合物

(βS)-β-氨基-4-(4-羟基苯氧基)-3,5-二碘苯甲丙醇 (S)-(-)-7'-〔4(S)-(苄基)恶唑-2-基]-7-二(3,5-二-叔丁基苯基)膦基-2,2',3,3'-四氢-1,1-螺二氢茚 (S)-盐酸沙丁胺醇 (S)-3-(叔丁基)-4-(2,6-二甲氧基苯基)-2,3-二氢苯并[d][1,3]氧磷杂环戊二烯 (S)-2,2'-双[双(3,5-三氟甲基苯基)膦基]-4,4',6,6'-四甲氧基联苯 (S)-1-[3,5-双(三氟甲基)苯基]-3-[1-(二甲基氨基)-3-甲基丁烷-2-基]硫脲 (R)富马酸托特罗定 (R)-(-)-盐酸尼古地平 (R)-(+)-7-双(3,5-二叔丁基苯基)膦基7''-[((6-甲基吡啶-2-基甲基)氨基]-2,2'',3,3''-四氢-1,1''-螺双茚满 (R)-3-(叔丁基)-4-(2,6-二苯氧基苯基)-2,3-二氢苯并[d][1,3]氧杂磷杂环戊烯 (R)-2-[((二苯基膦基)甲基]吡咯烷 (N-(4-甲氧基苯基)-N-甲基-3-(1-哌啶基)丙-2-烯酰胺) (5-溴-2-羟基苯基)-4-氯苯甲酮 (5-溴-2-氯苯基)(4-羟基苯基)甲酮 (5-氧代-3-苯基-2,5-二氢-1,2,3,4-oxatriazol-3-鎓) (4S,5R)-4-甲基-5-苯基-1,2,3-氧代噻唑烷-2,2-二氧化物-3-羧酸叔丁酯 (4-溴苯基)-[2-氟-4-[6-[甲基(丙-2-烯基)氨基]己氧基]苯基]甲酮 (4-丁氧基苯甲基)三苯基溴化磷 (3aR,8aR)-(-)-4,4,8,8-四(3,5-二甲基苯基)四氢-2,2-二甲基-6-苯基-1,3-二氧戊环[4,5-e]二恶唑磷 (2Z)-3-[[(4-氯苯基)氨基]-2-氰基丙烯酸乙酯 (2S,3S,5S)-5-(叔丁氧基甲酰氨基)-2-(N-5-噻唑基-甲氧羰基)氨基-1,6-二苯基-3-羟基己烷 (2S,2''S,3S,3''S)-3,3''-二叔丁基-4,4''-双(2,6-二甲氧基苯基)-2,2'',3,3''-四氢-2,2''-联苯并[d][1,3]氧杂磷杂戊环 (2S)-(-)-2-{[[[[3,5-双(氟代甲基)苯基]氨基]硫代甲基]氨基}-N-(二苯基甲基)-N,3,3-三甲基丁酰胺 (2S)-2-[[[[[[((1R,2R)-2-氨基环己基]氨基]硫代甲基]氨基]-N-(二苯甲基)-N,3,3-三甲基丁酰胺 (2-硝基苯基)磷酸三酰胺 (2,6-二氯苯基)乙酰氯 (2,3-二甲氧基-5-甲基苯基)硼酸 (1S,2S,3S,5S)-5-叠氮基-3-(苯基甲氧基)-2-[(苯基甲氧基)甲基]环戊醇 (1-(4-氟苯基)环丙基)甲胺盐酸盐 (1-(3-溴苯基)环丁基)甲胺盐酸盐 (1-(2-氯苯基)环丁基)甲胺盐酸盐 (1-(2-氟苯基)环丙基)甲胺盐酸盐 (-)-去甲基西布曲明 龙胆酸钠 龙胆酸叔丁酯 龙胆酸 龙胆紫 龙胆紫 齐达帕胺 齐诺康唑 齐洛呋胺 齐墩果-12-烯[2,3-c][1,2,5]恶二唑-28-酸苯甲酯 齐培丙醇 齐咪苯 齐仑太尔 黑染料 黄酮,5-氨基-6-羟基-(5CI) 黄酮,6-氨基-3-羟基-(6CI) 黄蜡,合成物 黄草灵钾盐