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3-bromononane | 690244-32-7

中文名称
——
中文别名
——
英文名称
3-bromononane
英文别名
3-Brom-nonan
3-bromononane化学式
CAS
690244-32-7
化学式
C9H19Br
mdl
——
分子量
207.154
InChiKey
SJKILSDODFBDFU-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

  • 沸点:
    95-97 °C(Press: 15 Torr)
  • 密度:
    1.0788 g/cm3

计算性质

  • 辛醇/水分配系数(LogP):
    4.8
  • 重原子数:
    10
  • 可旋转键数:
    6
  • 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:
    3-bromononane乙醚sodium 作用下, 生成 7,8-diethyl-tetradecane
    参考文献:
    名称:
    Petrow; Kaplan, Zhurnal Obshchei Khimii, 1942, vol. 12, p. 101
    摘要:
    DOI:
  • 作为产物:
    描述:
    (S)-壬烷-3-醇氢溴酸 作用下, 生成 3-bromononane
    参考文献:
    名称:
    Pickard; Kenyon, Journal of the Chemical Society, 1911, vol. 99, p. 55,71
    摘要:
    DOI:
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文献信息

  • Highly Efficient Oxidative Bromination of Alkanes with the HBr-H2O2 System in the Presence of Catalyst
    作者:Yujin Li、Jie Ju、Jianhong Jia、Weijian Sheng、Liang Han、Jianrong Gao
    DOI:10.1002/cjoc.201190016
    日期:2010.12
    straight‐chain alkanes were efficiently brominated with an aqueous HBr‐H2O2 system. This oxidative brominating process was promoted by catalysis and irradiation with light. The cycloalkanes were converted to the corresponding bromo‐cycloalkanes in moderate yields and the straight‐chain alkanes produced dominantly secondary bromides. This simple but effective bromination method of alkanes is characterized
    各种环烷烃和直链烷烃可通过HBr-H 2 O 2水溶液有效溴化。通过催化和光照射促进了该氧化溴化过程。环烷烃以中等收率转化为相应的溴代环烷烃,而直链烷烃则主要生成仲溴化物。这种简单而有效的烷烃溴化方法的特点是原子效率高,试剂价格便宜并且不存在有机废物,这使其成为现有的溴化CH活化方法的良好替代方法。
  • Bicyclic compounds and compostions as PDF inhibitors
    申请人:Molteni Valentina
    公开号:US20050197326A1
    公开(公告)日:2005-09-08
    This invention is directed to novel bicyclic compounds, to the uses of these compounds in various medicinal applications, including treating disorders amenable to treatment by peptidyl deformylase inhibitors such as treatment of bacterial infections, and to pharmaceutical compositions comprising these compounds.
    本发明涉及新型双环化合物,以及这些化合物在各种医学应用中的用途,包括治疗适用于肽脱甲基酰基酶抑制剂治疗的疾病,如细菌感染的治疗,并涉及包含这些化合物的制药组合物。
  • BICYCLIC COMPOUNDS AND COMPOSITIONS AS PDF INHIBITORS
    申请人:Molteni Valentina
    公开号:US20070259852A1
    公开(公告)日:2007-11-08
    This invention is directed to novel bicyclic compounds, to the uses of these compounds in various medicinal applications, including treating disorders amenable to treatment by peptidyl deformylase inhibitors such as treatment of bacterial infections, and to pharmaceutical compositions comprising these compounds.
    本发明涉及新型双环化合物、这些化合物在各种药物应用中的用途,包括治疗适用于肽形变酶抑制剂治疗的疾病,例如治疗细菌感染,并涉及包含这些化合物的制药组合物。
  • Compound, photocurable composition, cured product of same, printing ink, and printed matter curing the printing ink
    申请人:DIC Corporation
    公开号:US11079675B2
    公开(公告)日:2021-08-03
    A novel compound is used as a novel photopolymerization initiator, the novel compound having a molecular structure represented by general formula 1 below [R1 represents an alkyl group having 1 to 10 carbon atoms, R2 represents an alkyl group having 1 to 12 carbon atoms or the like, R3 represents an alkyl group having 1 to 12 carbon atoms or the like, R4 to R7 each independently represent a hydrogen atom, an alkyl group having 1 to 8 carbon atoms, or the like, Y1 represents an alkyl group having 3 to 19 carbon atoms or the like, Y2 represents an organic linking group, X1 represents an ethylene group or the like, X2 and X3 each represent an ethylene group or the like, Y3 represents a single bond or an alkylidene group, and n represents an integer of 1 to 3].
    一种新型化合物被用作新型光聚合引发剂,该新型化合物的分子结构如下通式 1 所示 [R1 代表具有 1 至 10 个碳原子的烷基,R2 代表具有 1 至 12 个碳原子的烷基或类似物,R3 代表具有 1 至 12 个碳原子的烷基或类似物,R4 至 R7 各自独立地代表氢原子、具有 1 至 8 个碳原子的烷基或类似物、Y1 代表具有 3 至 19 个碳原子的烷基或类似基团,Y2 代表有机连接基团,X1 代表乙烯基或类似基团,X2 和 X3 各自代表乙烯基或类似基团,Y3 代表单键或亚烷基,n 代表 1 至 3 的整数]。
  • The Synthesis of N-Substituted 2-Aminoethanethiosulfuric Acids
    作者:Daniel L. Klayman、W. Franklin Gilmore
    DOI:10.1021/jm00336a041
    日期:1964.11
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