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3,4,5,6-四氢-2,7-苯并二氧杂环癸烷e-1,8-二酮 | 29246-20-6

中文名称
3,4,5,6-四氢-2,7-苯并二氧杂环癸烷e-1,8-二酮
中文别名
——
英文名称
3,4,5,6-tetrahydrobenzo[c][1,6]dioxecine-1,8-dione
英文别名
3,4,5,6-Tetrahydro-2,7-benzodioxacyclodecen-1,8-dion;3,4,5,6-Tetrahydro-2,7-benzodioxecine-1,8-dione
3,4,5,6-四氢-2,7-苯并二氧杂环癸烷e-1,8-二酮化学式
CAS
29246-20-6
化学式
C12H12O4
mdl
——
分子量
220.225
InChiKey
CAWGQUPKYLTTNX-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):
    2.1
  • 重原子数:
    16
  • 可旋转键数:
    0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.33
  • 拓扑面积:
    52.6
  • 氢给体数:
    0
  • 氢受体数:
    4

SDS

SDS:9a5e8806c73f2ee338b6622f16aa51e7
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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

反应信息

  • 作为产物:
    描述:
    邻苯二甲酸二烯丙酯玻璃纤维增强塑料Grubbs catalyst first generation 作用下, 以 1,2-二氯乙烷 为溶剂, 反应 0.5h, 以79%的产率得到3,4,5,6-四氢-2,7-苯并二氧杂环癸烷e-1,8-二酮
    参考文献:
    名称:
    无溶剂条件下微波辅助钌催化的烯烃复分解
    摘要:
    建立了一种在无溶剂条件下通过微波活化进行开环复分解的有效方法。非热微波的特定作用是明显的。
    DOI:
    10.1016/j.tetlet.2003.10.049
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文献信息

  • Silver carboxylate promoted lactonization: a general method applicable to prepare medium and large-sized lactones without high dilution or slow addition
    作者:Le Liu、Shimin Xu、Hongwei Zhou
    DOI:10.1016/j.tet.2013.07.064
    日期:2013.9
    and simple operation, remains a challenging task for the organic community. We developed a ‘freshman-can-do’ protocol to medium- and large-sized lactones, not depending on high-dilution or slow addition techniques. Application of this method for the synthesis of natural lactones or potentially pharmaceutical compounds might be useful for organic chemists and pharmacists.
    对于有机内酯而言,有效且适用的宏观内酯化方法以及充足的起始原料和简单的操作方法仍然是一项艰巨的任务。我们为中型和大型内酯开发了“新鲜人可以做”的实验方案,而不依赖于高稀释或慢速添加技术。该方法用于天然内酯或潜在药物化合物的合成对于有机化学家和药剂师可能是有用的。
  • POLYESTER AMIDES AND ADHESIVES THEREFROM
    申请人:TORAY INDUSTRIES, INC.
    公开号:EP0042008A1
    公开(公告)日:1981-12-23
    Polyester amides constituted by (A) ester units mainly comprising benzenedicarboxylic acid and 1,4-butanediol and (B) amido units comprising dodecanamido and/or undecanamido units, with the weight ratio of said ester units to said amido units being 5 to 95:95 to 5, which have excellent mechanical strength, transparency, oil resistance, adhesiveness, and heat-sensitive characteristics, a process for their preparation, and an adhesive for fibers and metals comprising said polyester amides.
    由(A)主要由苯二甲酸和 1,4-丁二醇组成的酯单元和(B)由十二酰胺基和/或十一酰胺基单元组成的酰胺单元构成的聚酯酰胺,所述酯单元与所述酰胺单元的重量比为 5 至 95:95 至 5,具有优异的机械强度、透明度、耐油性、粘合性和热敏特性;其制备方法;以及由所述聚酯酰胺构成的纤维和金属粘合剂。
  • Method for producing polyesters
    申请人:TORAY INDUSTRIES, INC.
    公开号:EP0761713A2
    公开(公告)日:1997-03-12
    Disclosed is a method for producing polyesters by polymerizing terephthalic acid and/or its ester-forming derivative, and a glycol and/or its ester-forming derivative in a plant comprising an esterification device and a polycondensation device in series, while partly or wholly recycling the distillate from the esterification device and/or the polycondensation device that consists essentially of a glycol and/or its ester-forming derivative. The method comprises a step of continuously or intermittently measuring the content of at least one of water, the glycol and its ester-forming derivative in the distillate to be recycled, determining the amounts of the raw materials to be fed to the intended reaction device, on the basis of the data thus measured, and feeding the thus-determined amounts of the raw materials to the reaction device; or comprises a step of storing the distillate, prior to being recycled for the starting material, in a storing tank that has a capacity corresponding to the amount of the glycol and/or its ester-forming derivative to be fed to the esterification device for a period of 10 hours or more.
    本发明公开了一种通过聚合对苯二甲酸和/或其酯类衍生物以及乙二醇和/或其酯类衍生物来生产聚酯的方法,聚合装置包括一个串联的酯化装置和一个缩聚装置,同时部分或全部回收来自酯化装置和/或缩聚装置的主要由乙二醇和/或其酯类衍生物组成的馏分。该方法包括以下步骤:连续或间歇地测量待回收馏分中水、乙二醇及其酯形成衍生物中至少一种物质的含量,根据所测量的数据确定送入预定反应装置的原料量,并将由此确定的原料量送入反应装置;或包括一个步骤,即在回收馏出物作为起始原料之前,将其储存在一个储存罐中,该储存罐的容量与将送入酯化装置的乙二醇和/或其酯化衍生物的量相当,储存时间为 10 小时或更长时间。
  • THERMOPLASTIC POLYESTER RESIN COMPOSITION AND MOLDED ARTICLE
    申请人:DAICEL CHEMICAL INDUSTRIES, LTD.
    公开号:EP1591486A1
    公开(公告)日:2005-11-02
    A molded article of an aromatic polyester block copolymer-series resin is obtained, which is excellent in hydrolysis resistance, heat resistance, and yellowing resistance. There is used a polyester based thermoplastic resin composition comprising: 100 parts by weight of a polyester block copolymer (A) which is a reaction product of a thermoplastic aromatic polyester (a) and a lactone (b) and has a terminal carboxyl group in an amount of less than 5 mg-KOH/g as an acid number; 0.05 to 5 parts by weight of a polycarbodiimide compound (B); 0.05 to 5 parts by weight of a bifunctional or polyfunctional epoxy compound (C); 0.01 to 0.5 part by weight of a phenol-series antioxidant (D); and 0.01 to 0.5 part by weight of a sulfur-series antioxidant (E).
    一种芳香族聚酯嵌段共聚物系列树脂的成型品,具有优异的耐水解性、耐热性和耐黄变性。使用的聚酯基热塑性树脂组合物包括100 重量份的聚酯嵌段共聚物 (A),它是热塑性芳香族聚酯 (a) 和内酯 (b) 的反应产物,具有酸值小于 5 mg-KOH/g 的末端羧基;0.05至5份(重量)的聚碳二亚胺化合物(B);0.05至5份(重量)的双官能团或多官能团环氧化合物(C);0.01至0.5份(重量)的酚系列抗氧化剂(D);以及0.01至0.5份(重量)的硫系列抗氧化剂(E)。
  • Verwendung von Butylenterephtalat zur Herstellung thermoplastischen Zahnersatzes
    申请人:Heraeus Kulzer GmbH
    公开号:EP1714632A1
    公开(公告)日:2006-10-25
    Es werden die Verwendung zyklischen, oligomeren Butylenterephthalats (CBT™) zur Herstellung thermoplastischen Zahnersatzes oder zur Herstellung von Ausgangsmaterialien für thermoplastischen Zahnersatz beschrieben, ferner CBT™enthaltende Ausgangsmaterialien zur Herstellung thermoplastischen Zahnersatzes, sowie Verfahren zur Herstellung thermoplastischen Zahnersatzes.
    介绍了使用环状低聚对苯二甲酸丁二醇酯(CBT™)生产热塑性义齿或生产热塑性义齿的起始材料,以及含有 CBT™ 的用于生产热塑性义齿的起始材料和生产热塑性义齿的工艺。
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同类化合物

胰岛素原(cattle),29-[N6-[[2-(甲磺酰)乙氧基]羰基]-L-赖氨酸]-59-[N6-[[2-(甲磺酰)乙氧基]羰基]-L-赖氨酸]-(9CI) 十氢-2,7-苯并二氧杂环癸烷-3,6-二酮 二环<3.3.0>-2-氧杂-5-(2-丙烯基)-1-辛烯 乙烯邻苯二甲酸酯 [(E,1R)-1-[(2R,4Z,7S,8R)-7-溴-8-乙基-3,6,7,8-四氢-2H-氧杂环辛三烯-2-基]己-3-烯-5-炔基]乙酸酯 [(2R,3S,4E,6R,7S)-6,7-二羟基-2-甲基-10-氧代-2,3,6,7,8,9-六氢氧杂环辛三烯-3-基] (E)-丁-2-烯酸酯 6,7-二氢-5aH-氧杂环丁烷并[3,2-d][1,3]苯并二氧戊环 5-氧杂-10-氮杂三环[5.3.1.03,8]十一碳-1(10),2,6,8-四烯 3-氧杂二环[3.3.1]壬-6-烯-9-酮 3,4,5,6-四氢-2,7-苯并二氧杂环癸烷e-1,8-二酮 10-(乙酰氧基)-4,5,6,7-四氢-2H-1-苯并氧杂环辛三烯-2,8(3H)-二酮 1-(2,3,4,5-四氢-1,6-苯并二噁辛英-8-基)丙烷-1-酮 1,2-环己烷二甲酸1-甲基-1,2-乙二基酯 (S)-5-烯丙基-2-氧杂双环[3.3.0]辛-8-烯 (7Z)-2-(3-溴丙-1,2-二烯基)-5-(1-溴丙基)-3,3a,5,6,9,9a-六氢-2H-呋喃并[3,2-b]氧杂环辛三烯 (7E)-4,7-二羟基-10-甲基-3,4,5,6,9,10-六氢氧杂环辛三烯-2-酮 (6Z)-10-甲基-3,4,5,8,9,10-六氢-2H-氧杂环辛三烯-2-酮 (5Z,8S)-3-氯-2-[(E)-戊-2-烯-4-炔基]-8-[(E)-丙-1-烯基]-3,4,7,8-四氢-2H-氧杂环辛三烯 (4Z)-3,6-二氢-2,7-苯并二氧杂环癸烷e-1,8-二酮 (4S,5Z,7S,8S,10R)-4,7,8-三羟基-10-甲基-3,4,7,8,9,10-六氢氧杂环辛三烯-2-酮 (4R,5R,6Z,8S,10R)-4,5,8-三羟基-10-甲基-3,4,5,8,9,10-六氢氧杂环辛三烯-2-酮 (2R,5Z)-8a-[(R)-1-溴丙基]-3a-氯-3,4,7,8-四氢-2a-[(Z)-2-戊烯-4-炔基]-2H-氧杂环辛三烯 1,3,3a,6a-tetrahydro-5-pentyl-4H-cyclopentafuran-4-one trans-1-oxacyclodec-7-ene-2-one 2-epi-herbarumin II (RS)-5-methoxy-2,3,5,6-tetrahydro-8H-benzo[1,4,7]trioxecin β-heptenolactone stagonolide-E fumaric acid butanediyl ester aspinolide A (3R,4R,9S,10R,Z)-4,9-dihydroxy-3-methyl-10-pentyl-3,4,7,8,9,10-hexahydro-2H-oxecin-2-one prelaureatin 8-acetyl-4,4-dimethyl-2,6-dioxo-9-(2-methylpropyl)-2,3,4,5,6,8-hexahydrooxocino[2,3-c]pyrrole 5,6-benzo-2,3-diethoxy-4-oxo-2-hepten-7-olide 3,4,5,6-tetrahydro-oxocin-2-one (Z)-3-butyl-5,6,7,8-tetrahydro-2H-oxocin-2-one presaccharothriolide X 1-{2-[4,5-dihydro-1H-2-benzoxocin-(6Z)-ylidenemethyl]-allyl}-piperidine (R,Z)-8-(methoxymethoxy)-2,2,6,9-tetramethyl-5,6-dihydro-2H-benzo[b]oxocine 5-hydroxy-7R,11-heliannan-10-one 8-methoxy-2,2,6,9-tetramethyl-2H-1-benzoxocin-3(4H)-one 8-methoxy-2,2,6,9-tetramethyl-3,4,5,6-tetrahydro-2H-1-benzoxocin-3-ol (4S,5Z,10R)-4-hydroxy-10-methyl-3,4,7,8,9,10-hexahydro-2H-oxecin-2-one (4R)-9,11-bis(benzyloxy)-4-methyl-4,5,6,7-tetrahydro-1H-benzo[d]-oxecine-2,8-dione ethyl (4Z)-4-methyl-7,8-dihydro-1,3,6-trioxocine-5-carboxylate 4-hydroxy-10-(2-hydroxyethyl)-1,2-dihydro-4,12a-methanooxocino[4,5-b][1,4]benzodioxin-5-one 4-hydroxy-9-(2-hydroxyethyl)-1,2-dihydro-4,12a-methanooxocino[4,5-b][1,4]benzodioxin-5-one (7R,9R,5E)-7-hydroxy-9-propylnon-5-en-9-olide (6S,7R,9R)-6,7-dihydroxy-9-propylnon-4-eno-9-lactone 7-[2-(3,5-Dichloro-N-oxo-pyridin-4-yl)-1-oxoethyl]-10-methoxy-2,3,4,5-tetrahydro-1,6-benzodioxocine