1,10-dibromododecane | 782472-06-4

• 分子结构分类: 有机化合物 - 有机卤素化合物 - 有机溴化物
• 英文名称: 1,10-dibromododecane
• CAS: 782472-06-4
• 化学式: C₁₂H₂₄Br₂
• 分子量: 328.131
• InChiKey: OYCGESINDSOZTG-UHFFFAOYSA-N

物化性质

• 沸点：
  325.0±10.0 °C(Predicted)
• 密度：
  1.295±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  6.3
• 重原子数：
  14
• 可旋转键数：
  10
• 环数：
  0.0
• sp3杂化的碳原子比例：
  1.0
• 拓扑面积：
  0
• 氢给体数：
  0
• 氢受体数：
  0

反应信息

• 作为反应物：
  描述：

  1,10-dibromododecane 、 4-(癸基氧基)苯甲酸甲酯 在 potassium carbonate 作用下， 以7.0 g (70%)的产率得到4-(12-bromo-dodecyloxy)-benzaldehyde
  参考文献：
  名称：

  BENT-CORE LC DECORATED GOLD NANOCLUSTERS

  摘要：

  新型硫醇端基的弯曲核液晶（LCs）被用来装饰金纳米颗粒。硫乙酸酯或黄酮/黄原酸酯官能团被用来将液晶连接到金纳米颗粒上。这种弯曲核装饰的纳米颗粒可以溶解在弯曲核液晶基质中，提供极化系统，对施加的电场快速响应，并展现其他有趣和有用的光学和电光行为。

  公开号：

  US20110062385A1

文献信息

• METHODS AND COMPOSITIONS FOR TREATMENT OF DIABETES AND DYSLIPIDEMIA
  申请人：Khanna Ish

  公开号：US20120071528A1

  公开（公告）日：2012-03-22

  The invention is directed to novel compounds of Formula I: as well as its stereoisomers and/or pharmaceutically acceptable salts, for the treatment of diabetes and diabetes associated dyslipidemia.

  该发明涉及一种新型化合物的公式I：以及其立体异构体和/或药用盐，用于治疗糖尿病和与糖尿病相关的血脂异常。
• [EN] 1-IMIDAZOLYMETHYL-SUBSTITUTED-2-NAPHTOLS AND THEIR USE AS ACCELERATORS FOR LOW-TEMPERATURE CURING<br/>[FR] 1-IMIDAZOLYMETHYLE-SUBSTITUTE-2-NAPHTOLS ET LEUR UTILISATION EN TANT QU'ACCELERATEURS POUR UN DURCISSEMENT A FAIBLE TEMPERATURE
  申请人：HUNTSMAN ADV MAT SWITZERLAND

  公开号：WO2004092141A1

  公开（公告）日：2004-10-28

  Compounds of the general formulae (I) and (II): where R1, R2 and R3 each independently of one another are H; C1-17alkyl; C3-12cycloalkyl, optionally substituted by C1-4alkyl groups; C4-20cycloalkyl-alkyl, optionally substituted by C1-4alkyl groups; C6-10, aryl, optionally substituted by 1-3 C1-4alkyl groups, -CN, Hal, OH, or C1-10alkoxy; C7-15phenylalkyl, optionally substituted by 1-3 C1-­4alkyl groups; C3-12alkenyl; C3-12alkynyl; or aromatic or aliphatic C3-12acyl; R4, R5, R6, R7, R8, and R9 each independently of one another are H; C1-17alkyl; C3-12Ccycloalkyl, optionally substituted by C1-4alkyl groups; C4-­20cycloalkyl-alkyl, optionally substituted by C1-4alkyl groups; C6-10aryl, optionally substituted by 1-3 C1-4alkyl groups; C7-15phenylalkyl, optionally substituted by 1-3 C1-4alkyl groups; C3-17alkenyl; C3-12alkynyl; C1-12alkoxy; or OH; for formula (1) R is C1-12alkyl; C3-12cycloalkyl, optionally substituted by C1-4alkyl groups; C4-20cycloalkyl­alkyl, optionally substituted by C1-4alkyl groups; C6-10aryl, optionally substituted by 1-3 C1-4alkyl groups; C7­-15phenylalkyl, optionally substituted by 1-3 C1-4alkyl groups; C3-12alkenyl; or C3-12alkynyl; and for formula (II) n = 2 - 12; as accelerators in curable epoxy resin compositions which are used as a compression moulding compound, sinter powder, encapsulating system, or casting resin, or for producing prepregs and laminates having very good interlaminar shear strength values using the resin infusion method, wet layup method and injection methods, for producing components, especially components of large surface area.

  通式(I)和(II)的化合物：其中R1、R2和R3各自独立地为H；C1-17烷基；C3-12环烷基，可选地被C1-4烷基基团取代；C4-20环烷基-烷基，可选地被C1-4烷基基团取代；C6-10芳基，可选地被1-3个C1-4烷基基团，-CN，Hal，OH或C1-10烷氧基取代；C7-15苯基烷基，可选地被1-3个C1-4烷基基团取代；C3-12烯基；C3-12炔基；或芳香或脂肪C3-12酰基；R4、R5、R6、R7、R8和R9各自独立地为H；C1-17烷基；C3-12环烷基，可选地被C1-4烷基基团取代；C4-20环烷基-烷基，可选地被C1-4烷基基团取代；C6-10芳基，可选地被1-3个C1-4烷基基团取代；C7-15苯基烷基，可选地被1-3个C1-4烷基基团取代；C3-17烯基；C3-12炔基；C1-12烷氧基；或OH；对于式(1)，R为C1-12烷基；C3-12环烷基，可选地被C1-4烷基基团取代；C4-20环烷基烷基，可选地被C1-4烷基基团取代；C6-10芳基，可选地被1-3个C1-4烷基基团取代；C7-15苯基烷基，可选地被1-3个C1-4烷基基团取代；C3-12烯基；或C3-12炔基；对于式(II)，n = 2-12；作为可固化环氧树脂组合物的催化剂，该组合物用作压缩成型复合材料、烧结粉末、封装系统或浇注树脂，或用于使用树脂渗透法、湿层压法和注射法制备具有非常好的层间剪切强度值的预浸料和层压板，用于制造特别是大面积构件。
• Bent-core LC decorated gold nanoclusters
  申请人：Ridout & Maybee LLP

  公开号：US08092712B2

  公开（公告）日：2012-01-10

  Novel thiol-terminated bent-core liquid crystals (LCs) are used to decorate gold nanoparticles. Thioacetate or xanthate/xanthogenate functional groups are used to effect the attachment of the LCs to the gold nanoparticles. Such bent-core decorated nanoparticles may be dissolved in bent-core liquid crystal host media to provide polarizable systems which respond quickly to applied electric fields and exhibit other interesting and useful optical and electro-optic behaviour.

  使用新型硫醇末端的弯曲核液晶（LCs）来装饰金纳米颗粒。硫乙酸酯或黄药/黄原酸酯功能团被用于将LCs附着到金纳米颗粒上。这种装饰的弯曲核纳米颗粒可以溶解在弯曲核液晶宿主介质中，提供可极化的系统，对施加的电场快速响应，并表现出其他有趣和有用的光学和电光行为。
• 1-Imidazolymethyl -substituted -2-naphtols and their use as accelerators for low - temperature curing
  申请人：Weidmann Ulrich

  公开号：US20060211845A1

  公开（公告）日：2006-09-21

  Compounds of the general formulae (I) and (II): where R 1 , R 2 and R 3 each independently of one another are H; C1-17 alkyl; C 3-12 cycloalkyl, optionally substituted by C 1-4 alkyl groups; C 4-20 cycloalkyl-alkyl, optionally substituted by C 1-4 alkyl groups; C 6-10 , aryl, optionally substituted by 1-3 C 1-4 alkyl groups, —CN, Hal, OH, or C 1-10 alkoxy; C 7-15 phenylalkyl, optionally substituted by 1-3 C 1-4 alkyl groups; C 3-12 alkenyl; C 3-12 alkynyl; or aromatic or aliphatic C 3-12 acyl; R 4 , R 5 , R 6 , R 7 , R 8 , and R 9 each independently of one another are H; C 1-17 alkyl, C 3-12 Ccycloalkyl, optionally substituted by C 1-4 alkyl groups; C 4-20 cycloalkyl-alkyl, optionally substituted by C 1-4 alkyl groups; C 6-10 aryl, optionally substituted by 1-3 C 1-4 alkyl groups; C 7-15 phenylalkyl, optionally substituted by 1-3 C 1-4 alkyl groups; C 3-17 alkenyl; C 3-12 alkynyl; C 1-12 alkoxy; or OH; for formula (1) R is C 1-12 alkyl; C 3-12 cycloalkyl, optionally substituted by C 1-4 alkyl groups; C 4-20 cycloalkylalkyl; optionally substituted by C 1-4 alkyl groups; C 6-10 aryl, optionally substituted by 1-3 C 1- 4alkyl groups; C 7-15 phenylalkyl, optionally substituted by 1-3 C 1-4 alkyl groups; C 3-12 alkenyl; or C 3-12 alkynyl; and for formula (II) n=2-12; as accelerators in curable epoxy resin compositions which are used as a compression moulding compound, sinter powder, encapsulating system, or casting resin, or for producing prepregs and laminates having very good interlaminar shear strength values using the resin infusion method, wet layup method and injection methods, for producing components, especially components of large surface area.

  通式（I）和（II）的化合物： 其中 R 1 , R 2 和 R 3 各自独立地为 H； C1-17 烷基 3-12 环烷基，可选择被 C 1-4 烷基 4-20 环烷基-烷基，可选择被 C 1-4 烷基 6-10 芳基，可选择被 1-3 个 C 1-4 烷基、-CN、Hal、OH 或 C 1-10 烷氧基取代；C 7-15 苯基烷基，可选择被 1-3 个 C 1-4 烷基 3-12 烯基 3-12 炔基；或芳香族或脂肪族 C 3-12 酰基；R 4 , R 5 , R 6 , R 7 , R 8 和 R 9 各自独立地为 H 1-17 烷基、C 3-12 环烷基，任选被 C 1-4 烷基；C 4-20 环烷基烷基，可选择被 C 1-4 烷基 6-10 芳基，可选择被 1-3 个 C 1-4 烷基 7-15 苯基烷基，可选择被 1-3 个 C 1-4 烷基 3-17 烯基 3-12 炔基 1-12 烷氧基；或 OH；对于式(1)，R 是 C 1-12 烷基 3-12 环烷基，可选择被 C 1-4 烷基 4-20 环烷基烷基；可选择被 C 1-4 烷基 6-10 芳基，可选择被 1-3 个 C 1- 4 烷基 7-15 苯基烷基，可选择被 1-3 个 C 1-4 烷基 3-12 烯基；或 C 3-12 式 (II) n=2-12；作为可固化环氧树脂组合物中的促进剂，可用作压缩模塑化合物、烧结粉、封装系统或浇注树脂，或用于使用树脂灌注法、湿法铺层法和注射法生产层间剪切强度值非常高的预浸料和层压板，用于生产部件，尤其是大表面积部件。
• EP1613604A1
  申请人：——

  公开号：EP1613604A1

  公开（公告）日：2006-01-11