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

2,4,6-三(4-氰基苯基)-1,3,5-三嗪 | 6876-34-2

中文名称
2,4,6-三(4-氰基苯基)-1,3,5-三嗪
中文别名
——
英文名称
4,4',4''-[1,3,5]triazine-2,4,6-triyl-tris-benzonitrile
英文别名
2,4,6-Tri--1,3,5-triazin;2,4,6-Tri-(p-cyanophenyl)-s-triazin;2,4,6-Tris(4-cyanophenyl)-1,3,5-triazine;4-[4,6-bis(4-cyanophenyl)-1,3,5-triazin-2-yl]benzonitrile
2,4,6-三(4-氰基苯基)-1,3,5-三嗪化学式
CAS
6876-34-2
化学式
C24H12N6
mdl
——
分子量
384.399
InChiKey
ZYKRIYCYWOHUDV-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:
    504 °C
  • 沸点:
    707.2±70.0 °C(Predicted)
  • 密度:
    1.39±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    4.1
  • 重原子数:
    30
  • 可旋转键数:
    3
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    110
  • 氢给体数:
    0
  • 氢受体数:
    6

安全信息

  • 海关编码:
    2933699090

SDS

SDS:9891cb975c3f269e6f0d0e30da1b397a
查看

反应信息

  • 作为产物:
    描述:
    对苯二腈 在 zinc(II) chloride 作用下, 反应 48.0h, 以90%的产率得到2,4,6-三(4-氰基苯基)-1,3,5-三嗪
    参考文献:
    名称:
    基于共价三嗪的骨架(CTF)对水溶液中的表面活性剂的高吸附性能。
    摘要:
    来自1,4-二氰基苯(CTF-1)的碳质基于三嗪的共价骨架,可以从水溶液中吸附多达约4 gg(-1)的表面活性剂烷基聚乙二醇醚,C12EO7和十二烷基硫酸钠,SDS(c = 8.0 mmol L( -1))的重量是炭黑(Evonik的Printex L)重量吸收能力的20倍以上。高摄取量归因于CTF薄片剥落。考虑到CTF的热稳定性和化学稳定性,首次使用CTF吸附表面活性剂的研究表明,CTF对于从溶液中吸收物质特别有趣。
    DOI:
    10.1039/c4cc06393g
点击查看最新优质反应信息

文献信息

  • Nitrogen-Rich Covalent Triazine Frameworks as High-Performance Platforms for Selective Carbon Capture and Storage
    作者:Stephan Hug、Linus Stegbauer、Hyunchul Oh、Michael Hirscher、Bettina V. Lotsch
    DOI:10.1021/acs.chemmater.5b03330
    日期:2015.12.8
    The search for new efficient physisorbents for gas capture and storage is the objective of numerous ongoing researches in the realm of functional framework materials. Here we present the CO2 and H2 uptake capacities of nitrogen rich covalent triazine frameworks (CTFs) based on lutidine, pyrimidine, bipyridine, and phenyl units, showing superior gas uptakes and extremely high CO2 selectivities toward N2. The CO2 uptake of a bipyridine-CTF synthesized at 600 °C (5.58 mmol g–1, 273 K) is the highest reported for all CTFs so far and the second highest for all porous organic polymers (POPs). Moreover, the CO2 selectivity toward N2 of a nitrogen-rich pyrimidine-based CTF synthesized at 500 °C (Henry: 189, IAST: 502) is the highest reported for all POPs, and the H2 uptake of CTF1 synthesized at 600 °C at 1 bar (2.12 wt %, 77 K) is the highest found for all CTFs to date as well. With the wide range of sorption data at hand, we carve out general trends in the gas uptake behavior within the CTF family and nitrogen-containing porous polymers in general, revealing the dominant role of the micropore volume for maximum CO2 uptake, while we find that the nitrogen content is a secondary effect weakly enhancing the CO2 uptake. The latter, however, was identified as the main contributor to the high CO2/N2 selectivities found for the CTFs. Furthermore, ambient water vapor sorption has been tested for CTFs for the first time, confirming the highly hydrophilic nature of CTFs with high nitrogen content.
    寻找新的高效气体捕集与封存物理吸附剂是目前功能框架材料领域众多研究的目标。在此,我们介绍了基于鲁替丁、嘧啶、联吡啶和苯基单元的富氮共价三嗪框架(CTFs)对二氧化碳和 H2 的吸收能力,结果表明它们具有优异的气体吸收能力和极高的二氧化碳对 N2 的选择性。在 600 °C 下合成的联吡啶-CTF 的二氧化碳吸收率(5.58 mmol g-1,273 K)是迄今为止所有 CTF 中最高的,也是所有多孔有机聚合物(POP)中第二高的。此外,在 500 °C 下合成的富氮嘧啶基 CTF 对 N2 的 CO2 选择性(Henry:189,IAST:502)是所有 POPs 中最高的,而在 600 °C 1 bar 下合成的 CTF1 对 H2 的吸收率(2.12 wt %,77 K)也是迄今为止所有 CTFs 中最高的。有了这些广泛的吸附数据,我们可以看出 CTF 家族和一般含氮多孔聚合物气体吸收行为的总体趋势,揭示了微孔体积对二氧化碳最大吸收量的主导作用,同时我们发现氮含量只是次要效应,对二氧化碳吸收量的提高作用微弱。然而,后者被认为是 CTF 具有较高 /N2 选择性的主要原因。此外,我们还首次测试了 CTF 的环境蒸气吸附性,证实了高氮含量 CTF 的高亲性。
  • PRODUCTION METHOD OF XYLYLENEDIAMINE
    申请人:KUMANO Tatsuyuki
    公开号:US20100168474A1
    公开(公告)日:2010-07-01
    A method of producing xylylenediamine by the hydrogenation of dicyanobenzene obtained by the ammoxidation of xylene in a high yield while prolonging the catalyst life. In the method, a molten dicyanobenzene from which compounds having a boiling point lower than that of dicyanobenzene have been removed but compounds having a boiling point higher than that of dicyanobenzene are not removed is dissolved in a solvent containing liquid ammonia. By this dissolution, at least part of dicyanobenzene polymers precipitates as insolubles. The precipitates are removed by a solid-liquid separation. By subjecting the resulting solution containing the dicyanobenzene polymers in a reduced amount to hydrogenation, xylylenediamine is produced in a high yield and the life time of hydrogenation catalyst is prolonged.
    一种通过将二甲苯氧化产生的二基苯经氢化反应制备对二甲苯二胺的方法,能够高产率地生产,同时延长催化剂的寿命。该方法中,将已去除沸点低于二基苯的化合物但未去除沸点高于二基苯的化合物的熔融二基苯溶于含有液的溶剂中。通过这种溶解,至少部分二基苯聚合物沉淀为不溶性物质。通过固液分离去除沉淀物。将含有少量二基苯聚合物的产物溶液进行还原反应,可以高产率地制备对二甲苯二胺,并延长氢化催化剂的使用寿命。
  • METHOD OF PREPARING ORGANIC POROUS SOLIDS AND SOLIDS OBTAINABLE BY THIS METHOD
    申请人:Antonietti Markus
    公开号:US20100280216A1
    公开(公告)日:2010-11-04
    The present invention relates to a method of preparing porous solids, which method comprises polymerizing, in a salt melt or a eutectic mixture of salt melt containing at least one Lewis acidic salt, cyano monomers having at least one or at least two cyano groups in their molecule, wherein the at least one or at least two cyano groups are bonded to a rigid linking group in the cyano monomer, as well as to the porous solids obtainable by that method. Owing to their porosity and the associated extremely high specific surface area, the porous solids are useful as sorbents, filtering and insulating materials, as well as catalyst carriers.
    本发明涉及一种制备多孔固体的方法,该方法包括在含有至少一种Lewis酸性盐的盐熔体或盐熔体共晶混合物中聚合至少含有一个或至少两个基团的基单体,其中至少一个或至少两个基团与基单体中的刚性连接基结合,以及由该方法获得的多孔固体。由于其多孔性和相关的极高比表面积,多孔固体可用作吸附剂、过滤和绝缘材料以及催化剂载体。
  • ELECTROACTIVE COMPOSITION
    申请人:Rostovtsev Vsevolod
    公开号:US20130299807A1
    公开(公告)日:2013-11-14
    There is provided an electroactive composition including (a) a host, (b) a dopant, and (c) an additive having Formula I In Formula I, E is the same or different at each occurrence and is N or C—Ar 1 and Ar 1 is the same or different at each occurrence and is H, D, or aryl. At least one E=N, and at least one Ar 1 is aryl.
    提供了一种电活性组合物,包括(a)宿主,(b)掺杂剂和(c)具有I式的添加剂。在I式中,E在每次出现时相同或不同,且为N或C-Ar1,而Ar1在每次出现时相同或不同,且为H、D或芳基。至少一个E为N,至少一个Ar1为芳基。
  • Production method of xylylenediamine
    申请人:Mitsubishi Gas Chemical Company, Inc.
    公开号:EP2202218A1
    公开(公告)日:2010-06-30
    A method of producing xylylenediamine by the hydrogenation of dicyanobenzene obtained by the ammoxidation of xylene in a high yield while prolonging the catalyst life. In the method, a molten dicyanobenzene from which compounds having a boiling point lower than that of dicyanobenzene have been removed but compounds having a boiling point higher than that of dicyanobenzene are not removed is dissolved in a solvent containing liquid ammonia. By this dissolution, at least part of dicyanobenzene polymers precipitates as insolubles. The precipitates are removed by a solid-liquid separation. By subjecting the resulting solution containing the dicyanobenzene polymers in a reduced amount to hydrogenation, xylylenediamine is produced in a high yield and the life time of hydrogenation catalyst is prolonged.
    一种通过二甲苯氧化反应制得的二基苯的氢化反应生产二甲苯二胺的方法,该方法产率高,同时可延长催化剂寿命。在该方法中,将已除去沸点低于二基苯的化合物但未除去沸点高于二基苯的化合物的熔融二基苯溶解在含有液的溶剂中。通过这种溶解,至少有一部分二基苯聚合物以不溶物的形式沉淀下来。沉淀物通过固液分离去除。将所得的含有少量二基苯聚合物的溶液进行氢化,可生产出高产率的二甲苯,并延长氢化催化剂的使用寿命。
查看更多

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,S)-邻甲苯基-DIPAMP (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)-(-)-4,12-双(二苯基膦基)[2.2]对环芳烷(1,5环辛二烯)铑(I)四氟硼酸盐 (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)-(+)-7-双(3,5-二叔丁基苯基)膦基7''-[(4-叔丁基吡啶-2-基甲基)氨基]-2,2'',3,3''-四氢-1,1''-螺双茚满 (R)-(+)-7-双(3,5-二叔丁基苯基)膦基7''-[(3-甲基吡啶-2-基甲基)氨基]-2,2'',3,3''-四氢-1,1''-螺双茚满 (R)-(+)-4,7-双(3,5-二-叔丁基苯基)膦基-7“-[(吡啶-2-基甲基)氨基]-2,2”,3,3'-四氢1,1'-螺二茚满 (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 (R)-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 (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 (4S,4''S)-2,2''-亚环戊基双[4,5-二氢-4-(苯甲基)恶唑] (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 (3aR,6aS)-5-氧代六氢环戊基[c]吡咯-2(1H)-羧酸酯 (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-[[[[[((1S,2S)-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 (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 (1S,2S,3R,5R)-2-(苄氧基)甲基-6-氧杂双环[3.1.0]己-3-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 (1-(2,6-二氟苯基)环丙基)甲胺盐酸盐 (-)-去甲基西布曲明 龙蒿油 龙胆酸钠 龙胆酸叔丁酯 龙胆酸 龙胆紫-d6 龙胆紫