5-butyl-5-chlorononane | 100529-14-4

• 分子结构分类: 有机化合物 - 有机卤素化合物 - 有机氯化物
• 英文名称: 5-butyl-5-chlorononane
• 英文别名: 5-Butyl-5-chlor-nonan；Tributylchlormethan
• CAS: 100529-14-4
• 化学式: C₁₃H₂₇Cl
• 分子量: 218.81
• InChiKey: IZAYULCVPJGMJM-UHFFFAOYSA-N

物化性质

• 沸点：
  91.5-92.5 °C(Press: 2.5 Torr)
• 密度：
  0.8701 g/cm3

计算性质

• 辛醇/水分配系数(LogP)：
  6.1
• 重原子数：
  14
• 可旋转键数：
  9
• 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：

  5-butyl-5-chlorononane 生成 5-丁基-4-壬烯
  参考文献：
  名称：

  Isomerization of Olefins. I. Conversion of t-Butylethylene, unsym-Methylisopropylethylene and Tetramethylethylene to Equilibrium Mixtures of the Three Olefins¹

  摘要：

  DOI：

  10.1021/ja01321a056
• 作为产物：
  描述：

  戊酸乙酯 在 盐酸 作用下， 生成 5-butyl-5-chlorononane
  参考文献：
  名称：

  Desgrandchamps,G. et al., Bulletin de la Societe Chimique de France, 1961, p. 264 - 268

  摘要：

  DOI：

文献信息

• Efficient TBAI-CS₂ Promoted Synthesis of Substituted Hydrazinecarbodithiolates
  作者：Nitin Srivastava

  DOI：10.1080/00304948.2022.2111171

  日期：2022.11.2

  Published in Organic Preparations and Procedures International: The New Journal for Organic Synthesis (Vol. 54, No. 6, 2022)

  发表于国际有机制剂和程序：有机合成新期刊（印刷前，2022 年）
• METHOD FOR PRODUCING POLYMER, POLYMER, COMPOSITION FOR FORMING INSULATING FILM, METHOD FOR PRODUCING INSULATING FILM, AND INSULATING FILM
  申请人：JSR Corporation

  公开号：EP1705206A1

  公开（公告）日：2006-09-27

  There are provided a method for producing a polymer, a polymer, an insulating-film-forming composition, a method for producing an insulating film, and an insulating film capable of forming a film which is suitably used as an interlayer dielectric for semiconductor devices or the like and exhibits a low relative dielectric constant, excellent mechanical strength and adhesion, and uniform quality. A method for producing a polymer of the invention comprises hydrolyzing and condensing (B) a hydrolyzable-group-containing silane monomer in the presence of (A) a polycarbosilane, the polycarbosilane (A) being a polymer (I) obtained by reacting (a) a compound shown by the following general formula (1) and (b) at least one compound selected from the group consisting of a compound shown by the following general formula (2) and a compound shown by the following general formula (3) in an organic solvent in the presence of at least one of an alkali metal and an alkaline earth metal,         R1kCX4-k     (1)         R2kSiY4-k     (2)         R3mY3-mSiCR4nX3-n     (3) wherein R1 to R4 individually represent a monovalent organic group or a hydrogen atom, X represents a halogen atom, Y represents a halogen atom or an alkoxy group, k represents an integer from 0 to 3, and m and n individually represent integers from 0 to 2.

  本发明提供了一种聚合物的生产方法、一种聚合物、一种绝缘成膜组合物、一种绝缘膜的生产方法，以及一种能够形成薄膜的绝缘膜，该薄膜适合用作半导体器件或类似器件的层间电介质，并具有较低的相对介电常数、优异的机械强度和附着力以及均匀的质量。 生产本发明聚合物的方法包括在（A）聚碳酸酯硅烷存在下水解和缩合（B）含可水解基团的硅烷单体、聚碳硅烷(A)为聚合物(I)，由(a)下式(1)所示化合物和(b)至少一种选自下式(2)所示化合物和下式(3)所示化合物组成的组的化合物在有机溶剂中，在碱金属和碱土金属中至少一种存在下反应而得、 R1kCX4-k (1) R2kSiY4-k (2) R3mY3-mSiCR4nX3-n (3) 其中 R1 至 R4 分别代表一价有机基团或氢原子，X 代表卤素原子，Y 代表卤素原子或烷氧基，k 代表 0 至 3 的整数，m 和 n 分别代表 0 至 2 的整数。
• Tschel'zowa et al., Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, 1955, p. 522,526; engl.Ausg.S. 459, 462
  作者：Tschel'zowa et al.

  DOI：——

  日期：——
• The Treatment of Facial Verrucae With the Pulsed Dye Laser
  作者：Hannah Vargas、Christopher R. Hove、Marsha L. Dupree、Edwin F. Williams

  DOI：10.1097/00005537-200209000-00007

  日期：2002.9

  AbstractObjectives/Hypothesis To evaluate the treatment of facial verrucae with the pulsed dye laser.Study Design A prospective, nonrandomized, nonblinded pilot study evaluating the treatment of facial verrucae with the pulsed dye laser.Methods Twelve patients with facial verrucae (four recalcitrant) were identified and followed in the study in the setting of a tertiary referral center. The treatment consisted of the flash‐lamp pumped pulsed dye laser (585 mn) with a spot size of 5 mm at fluences between 9.0 and 13 J/cm2. Each lesion received one or two pulses with 2 mm of surrounding normal skin included in the treatment. One patient had paring prior to pulse treatment. The patients were examined 3 to 4 weeks after each procedure, and clinical assessment of the lesion was documented.Results Patient ages ranged from 18 to 47 years. Four patients had refractory lesions, and eight patients had never undergone previous treatment. All 12 patients had full resolution of their facial warts after one to three treatment sessions. No complications such as scarring, alopecia, or recurrence were encountered. Follow‐up ranged from 10 to 33 months.Conclusions Pulsed dye laser therapy is highly effective and safe therapy for facial verrucae. This method appears to selectively destroy warts without damaging surrounding skin.
• Petrow; Tschernyschew, Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, 1952, p. 1082,1083
  作者：Petrow、Tschernyschew

  DOI：——

  日期：——