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

Isophthalic anhydride | 4891-67-2

中文名称
——
中文别名
——
英文名称
Isophthalic anhydride
英文别名
3-oxabicyclo[3.3.1]nona-1(9),5,7-triene-2,4-dione
Isophthalic anhydride化学式
CAS
4891-67-2
化学式
C8H4O3
mdl
——
分子量
148.11
InChiKey
LNYYKKTXWBNIOO-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):
    1.3
  • 重原子数:
    11
  • 可旋转键数:
    0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    43.4
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

  • 作为反应物:
    描述:
    Isophthalic anhydride 以90%的产率得到
    参考文献:
    名称:
    SARAF, S. D., SYNTH. COMMUN., 1983, 13, N 1, 7-14
    摘要:
    DOI:
点击查看最新优质反应信息

文献信息

  • PRODUCTION OF IONIC LIQUIDS
    申请人:Buchanan Charles Michael
    公开号:US20080194834A1
    公开(公告)日:2008-08-14
    Ionic liquids and processes and apparatus for their production. The ionic liquids can be low sulfur and low halide carboxylated ionic liquids. The ionic liquids can be produced via formation of at least one intermediate carboxylated ionic liquid, and thereafter subjecting the intermediate carboxylated ionic liquid to at least one anion exchange process.
    离子液体及其生产的方法和装置。这些离子液体可以是低硫和低卤代羧酸盐离子液体。这些离子液体可以通过形成至少一种中间羧酸盐离子液体,然后将中间羧酸盐离子液体经过至少一次阴离子交换过程来生产。
  • [EN] COMPOSITIONS AND METHODS FOR INHIBITING GROUP II INTRON RNA<br/>[FR] COMPOSITIONS ET MÉTHODES POUR INHIBER DES ARN D'INTRON DE GROUPE II
    申请人:UNIV YALE
    公开号:WO2019147894A1
    公开(公告)日:2019-08-01
    The present invention provides compositions and methods for inhibiting group II intron splicing for treating or preventing a disease or disorder associated with an organism harboring an active group II intron. The present invention also provides compositions and methods for inhibiting group II intron splicing for inhibiting, preventing or reducing growth of an organism harboring an active group II intron.
    本发明提供了用于抑制II类内含子剪接的组合物和方法,用于治疗或预防与携带活跃II类内含子的生物体相关的疾病或紊乱。本发明还提供了用于抑制II类内含子剪接,以抑制、预防或减少携带活跃II类内含子的生物体生长的组合物和方法。
  • Organophotoreceptor with charge transport compound having an epoxy group
    申请人:——
    公开号:US20040081903A1
    公开(公告)日:2004-04-29
    This invention relates to a novel organophotoreceptor that comprises an electrically conductive substrate and photoconductive element on the electrically conductive substrate, the photoconductive element having a) a novel charge transport compound having the formula 1 where X is a divalent hydrocarbon group of 1 to 30 carbon atoms, or a divalent hydrocarbon group of 1 to 30 carbon atoms where there is at least one substitution of a carbon atom by a heteroatom provided that no two heteroatoms may be adjacent within the backbone of an aliphatic divalent hydrocarbon radical, R 1 is an aryl group or a heterocyclic group, R 2 is a (N,N-disubstituted)arylamine group, and R 3 is an epoxy group; and (b) a charge generating compound. The epoxy group can be reacted with a functional group within the polymer to form a polymeric charge transport compound either directly or through a crosslinking agent.
    这项发明涉及一种新型的有机光感受器,包括具有电导基底和电导元件的电导基底上的光导元件,所述光导元件具有a) 具有以下结构式1的新型电荷传输化合物,其中X是1至30个碳原子的二价碳氢基团,或者是1至30个碳原子的二价碳氢基团,其中至少有一个碳原子被杂原子取代,前提是在脂肪族二价碳氢基团的骨架内不得有两个相邻的杂原子,R1是芳基或杂环基,R2是(N,N-二取代)芳胺基团,R3是环氧基;以及b) 一个电荷生成化合物。环氧基可以与聚合物内的功能基团反应,直接或通过交联剂形成聚合物电荷传输化合物。
  • METHOD FOR PRODUCING THIOESTER GROUP-CONTAINING ORGANOSILICON COMPOUND, THIOESTER GROUP-CONTAINING ORGANOSILICON COMPOUND, COMPOUNDING AGENT FOR RUBBER, RUBBER COMPOSITION, AND TIRE
    申请人:TSUCHIDA Kazuhiro
    公开号:US20120296023A1
    公开(公告)日:2012-11-22
    A new method for producing a thioester group-containing organosilicon compound by a convenient reaction with dramatically improved workability generating reduced byproduct is provided. The method comprises reacting an organosilicon compound having a hydrolyzable silyl group and mercapto group with a carboxylic anhydride. Also provided are an organosilicon compound having a hydrolyzable silyl group, a thioester group, and carboxyl group in the same molecule capable of remarkably reducing hysteresis loss of the cured rubber composition; a compounding agent for rubber containing such organosilicon compound; a rubber composition prepared by blending such compounding agent for rubber; and a tire produced by using the cured rubber composition are also provided.
    提供一种通过方便的反应生成减少副产物的硫酯基含有的有机硅化合物的新方法。该方法包括将具有可水解硅基和巯基的有机硅化合物与羧酸酐反应。还提供了一种具有同一分子中可水解硅基、硫酯基和羧基的有机硅化合物,能显著减少固化橡胶组合物的滞后损失;一种含有此类有机硅化合物的橡胶配方剂;通过混合此类橡胶配方剂制备的橡胶组合物;以及使用固化橡胶组合物生产的轮胎。
  • ANTI-BLUE LIGHT COMPOUND, PREPARATION METHOD AND APPLICATION THEREOF
    申请人:EUTEC NEW MATERIALS TECHNOLOGY (SUZHOU) CO., LTD.
    公开号:US20210230128A1
    公开(公告)日:2021-07-29
    Disclosed is a blue light absorbing compound, its preparation method and use. The compound has high stability and is suitable for high temperature processing conditions as well as outdoor application. A method of covalently bonding a blue light absorbing compound with an ultraviolet light absorbing compound for increasing its stability is also provided. The compound is capable of absorbing or blocking ultraviolet light (UVA, UVB) and blue light to protect eyes. But long-wavelength blue light can be absorbed diminishingly, so that the transmitted light has a particularly good visual experience.
    揭示了一种蓝光吸收化合物,其制备方法和用途。该化合物具有高稳定性,适用于高温加工条件以及户外应用。还提供了一种通过共价键合蓝光吸收化合物和紫外线吸收化合物以增加其稳定性的方法。该化合物能够吸收或阻挡紫外线光(UVA,UVB)和蓝光以保护眼睛。但是长波长的蓝光可以被吸收得很少,使得透过的光具有特别好的视觉体验。
查看更多

同类化合物

2,9-二(2-苯乙基)蒽并[2,1,9-DEF:6,5,10-D’E’F’]二异喹啉-1,3,8,10(2H,9H)-四酮 (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)-(+)-5,5'',6,6'',7,7'',8,8''-八氢-3,3''-二叔丁基-1,1''-二-2-萘酚,双钾盐 (S)-盐酸沙丁胺醇 (S)-7,7-双[(4S)-(苯基)恶唑-2-基)]-2,2,3,3-四氢-1,1-螺双茚满 (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-N-Fmoc-氨基甲基吡咯烷盐酸盐 (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)-7,7-双[(4S)-(苯基)恶唑-2-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)-3,3''-双([[1,1''-联苯]-4-基)-[1,1''-联萘]-2,2''-二醇 (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 (4S,5R)-3,3a,8,8a-四氢茚并[1,2-d]-1,2,3-氧杂噻唑-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 (3aS,8aR)-2-(吡啶-2-基)-8,8a-二氢-3aH-茚并[1,2-d]恶唑 (3aS,3''aS,8aR,8''aR)-2,2''-环戊二烯双[3a,8a-二氢-8H-茚并[1,2-d]恶唑] (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 (3S,3aR)-2-(3-氯-4-氰基苯基)-3-环戊基-3,3a,4,5-四氢-2H-苯并[g]吲唑-7-羧酸 (3R,3’’R,4S,4’’S,11bS,11’’bS)-(+)-4,4’’-二叔丁基-4,4’’,5,5’’-四氢-3,3’’-联-3H-二萘酚[2,1-c:1’’,2’’-e]膦(S)-BINAPINE (3-三苯基甲氨基甲基)吡啶 (3-[(E)-1-氰基-2-乙氧基-2-hydroxyethenyl]-1-氧代-1H-茚-2-甲酰胺) (2Z)-3-[[(4-氯苯基)氨基]-2-氰基丙烯酸乙酯 (2S,4S)-Fmoc-4-三氟甲基吡咯烷-2-羧酸 (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,3R)-3-(叔丁基)-2-(二叔丁基膦基)-4-甲氧基-2,3-二氢苯并[d][1,3]氧杂磷杂戊环 (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''S,3S,3''S)-3,3''-二叔丁基-4,4''-二甲氧基-2,2'',3,3''-四氢-2,2''-联苯并[d][1,3]氧杂磷杂戊环 (2S,2''S,3S,3''S)-3,3''-二叔丁基-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 (2R,2''R,3R,3''R)-3,3''-二叔丁基-4,4''-二甲氧基-2,2'',3,3''-四氢-2,2''-联苯并[d][1,3]氧杂磷杂戊环 (2-硝基苯基)磷酸三酰胺 (2-氯-6-羟基苯基)硼酸 (2-氟-3-异丙氧基苯基)三氟硼酸钾 (2,6-二氯苯基)乙酰氯 (2,3-二甲氧基-5-甲基苯基)硼酸 (1α,1'R,4β)-4-甲氧基-5''-甲基-6'-[5-(1-丙炔基-1)-3-吡啶基]双螺[环己烷-1,2'-[2H]indene (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 (1R,1′R,2S,2′S)-2,2′-二叔丁基-2,3,2′,3′-四氢-1H,1′H-(1,1′)二异磷哚