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1,11-dichloroundecane | 822-07-1

中文名称
——
中文别名
——
英文名称
1,11-dichloroundecane
英文别名
——
1,11-dichloroundecane化学式
CAS
822-07-1
化学式
C11H22Cl2
mdl
——
分子量
225.202
InChiKey
FFYJIEDNUOXZJY-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):
    5.5
  • 重原子数:
    13
  • 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

SDS

SDS:6f48bee4a2bfc93d5dcd73055c4be372
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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
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    1,11-dichloroundecane乙醇 、 sodium iodide 作用下, 生成 tridecanedinitrile
    参考文献:
    名称:
    Tibolone Exerts Its Protective Effect on Trabecular Bone Loss Through the Estrogen Receptor
    摘要:
    替泊龙(Org OD14)根据组织类型具有雌激素样、孕激素样和/或雄激素样的活性。在绝经后女性中,替泊龙可以防止骨质流失,而不会刺激子宫内膜。替泊龙通过减少骨代谢,即骨吸收,像雌激素一样有效地预防年轻和年老卵巢切除(OVX)大鼠的周围和轴骨的骨小梁流失。我们评估了各种激素活性对替泊龙维持骨骼的贡献。三个月大的OVX大鼠接受替泊龙(每只125微克或500微克,双次每日),单独或与抗雌激素、抗雄激素或抗孕激素联合用药,评估其对骨小梁骨质量和骨代谢的影响。假手术和对照OVX组接受车辆处理。其余OVX组每天口服替泊龙,单独或与(a)抗雌激素ICI 164.384,(b)抗雄激素氟他胺,或(c)抗孕激素Org 31710联合用药。为了比较,17β-雌二醇和睾酮的效果也进行了研究。经过4周的处理后,测定了远端股骨的骨小梁矿物质密度(BMD)、血浆骨钙素和尿液去氧吡啶酮/肌酐比率(Dpyr/Cr)。替泊龙或17β-雌二醇显著阻止了卵巢切除所致的骨小梁BMD减少,并通过降低Dpyr/Cr比率和骨钙素分别抑制了骨吸收和骨代谢。这两种化合物的效果均被抗雌激素所抵消。这表明雌激素受体在替泊龙影响骨代谢中的主要作用。然而,抗雄激素和抗孕激素并未抵消替泊龙的作用,排除了替泊龙的雄激素样和孕激素样活性对其抗骨小梁流失作用的主要角色。结果表明,替泊龙几乎完全通过激活雌激素受体来影响骨骼。
    DOI:
    10.1359/jbmr.2001.16.9.1651
  • 作为产物:
    描述:
    参考文献:
    名称:
    Synthesis and pharmacological properties of bisquaternary salts of α,ω-Di[N-methyl-N-(1-adamantyl)amino] alkanes
    摘要:
    DOI:
    10.1007/bf00771468
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文献信息

  • Catalytic remote hydrohalogenation of internal alkenes
    作者:Xiang Li、Jianbo Jin、Pinhong Chen、Guosheng Liu
    DOI:10.1038/s41557-021-00869-x
    日期:2022.4
    alkene isomers. Here we report the remote oxidative halogenation of alkenes under palladium catalysis via which both terminal and internal alkenes yield primary alkyl halides efficiently. Engineering pyridine-oxazoline ligands by introducing a hydroxyl group is essential for achieving excellent chemo- and regioselectivity. The catalytic system is also good for the mixture of alkene isomers generated from
    伯烷基卤化物在有机合成中作为精细化学品具有广泛的用途。烯烃的直接卤化是合成这些卤化物的最有效方法之一。内部烯烃,特别是来自炼油厂的异构体混合物,构成了容易获得且廉价的原料,并且是该合成最有吸引力的起始材料。然而,烯烃的卤化氢通常会产生支链烷基卤化物。没有直接从内部烯烃制备直链烷基卤化物的催化方法,更不用说从烯烃异构体的混合物中制备了。在这里,我们报告了在钯催化下烯烃的远程氧化卤化,末端和内部烯烃都可以有效地产生伯烷基卤化物。通过引入羟基来设计吡啶-恶唑啉配体对于实现出色的化学和区域选择性至关重要。该催化体系也适用于烷烃脱氢生成的烯烃异构体混合物,为研究廉价烷烃的高价值利用提供了窗口。
  • [EN] BIOMASS-DERIVED POLYMERS AND COPOLYMERS INCORPORATING MONOLIGNOLS AND THEIR DERIVATIVES<br/>[FR] POLYMÈRES ET COPOLYMÈRES D'ORIGINE BIOMASSIQUE CONTENANT DES MONOLIGNOLS ET LEURS DÉRIVÉS
    申请人:UNIV CALIFORNIA
    公开号:WO2017066699A1
    公开(公告)日:2017-04-20
    The invention includes methods and materials for forming and manipulating aromatic-based polymers and copolymers using biomass compounds as starting materials. Embodiments of the invention can be used in processes designed to replace those used in the petrochemical industry. Typical embodiments of the invention include methods and materials for forming and/or modifying compounds including dicarboxylic acid ester dimers, benzoxazines and dicarboxylic acid ether dimers. Embodiments of the invention further provide methods and materials for utilizing these compounds to form commercially desirable polymers having structures and physical properties akin to those found in polymers formed from petroleum products.
    该发明涉及利用生物质化合物作为起始材料形成和操纵芳香基聚合物和共聚物的方法和材料。该发明的实施方式可用于设计用以取代石油化工行业所使用的工艺。该发明的典型实施方式包括形成和/或修改化合物的方法和材料,包括二羧酸酯二聚体、苯并噁唑和二羧酸醚二聚体。该发明的实施方式还提供利用这些化合物形成具有商业上理想结构和物理性质的聚合物的方法和材料,这些聚合物的结构和物理性质类似于由石油制品形成的聚合物。
  • Method for producing coupling compound
    申请人:Sumitomo Chemical Company, Limited
    公开号:US20040161404A1
    公开(公告)日:2004-08-19
    There are disclosed a method for producing a cross-coupling compound of formula (3): (Y—) (n−1) R 1 —R 2 —(R 1 ) (n′−1) (3) wherein R 1 represents a substituted or unsubstituted, linear, branched, or cyclic hydrocarbon group, and n and n′ each represent 1 or 2, provided that when n and n′ are the same, both n and n′ are not 2, R 2 represents a substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl or substituted or unsubstituted alkenyl group, and Y represents R 2 or X 1 , wherein R 2 is as defined above, and X 1 represents a chlorine, bromine or iodine atom, which method comprises reacting an organic halide of formula (1): n′(R 1 X l n ), wherein R 1 is as defined above and carbon atoms at the &agr; and &bgr; positions relative to X 1 are sp 3 carbon atoms, and X 1 , n and n′ are as defined above, with a boron compound of formula (2): m{R 2 (BX 2 2 ) n′ }, wherein R 2 and n′ are as defined above, X 2 independently represents a hydroxyl group or an alkoxy or aryloxy group, or X 2 2 together form an alkoxy or aryloxy group, and m represents 1 or 2, and m≧n, and the boron atom is bonded with a sp 2 carbon atom of R 2 group, or a boronic acid trimer anhydride thereof, in the presence of a base and a catalyst comprising a nickel compound and a compound of formula (i): 1 wherein R 3 represents a substituted or unsubstituted alkyl group, R 4 represents a hydrogen atom or an substituted or unsubstituted alkyl group, l represents an integer of 1 to 3, and p and q each represents an integer of 0 to 2; and a catalyst.
    本发明公开了一种制备交叉偶联化合物的方法,该化合物的化学式为(3):(Y-)(n-1)R1-R2-(R1)(n' -1)(3),其中R1代表取代或未取代的线性、支链或环烃基,n和n'各自代表1或2,但当n和n'相同时,n和n'均不为2;R2代表取代或未取代的芳基、取代或未取代的杂环基或取代或未取代的烯基,Y代表R2或X1,其中R2如上所定义,X1代表氯、溴或碘原子。该方法包括将化学式为(1)的有机卤化物与化学式为(2)的硼化合物在碱和催化剂的存在下反应,其中化学式(1)中R1如上所定义,X1、n和n'如上所定义,α和β位置相对于X1的碳原子为sp3碳原子,化学式(2)中R2和n'如上所定义,X2独立代表羟基或烷氧基或芳氧基,或X22共同形成烷氧基或芳氧基,m代表1或2,m≤n,硼原子与R2基的sp2碳原子或其硼酸三聚体酐键合。催化剂包括一种镍化合物和一种化学式为(i)的化合物:1其中R3代表取代或未取代的烷基,R4代表氢原子或取代或未取代的烷基,l代表1至3的整数,p和q分别代表0至2的整数。
  • METHOD FOR PRODUCING COUPLING COMPOUND
    申请人:Itahashi Tamon
    公开号:US20060281925A1
    公开(公告)日:2006-12-14
    A method is provided for producing a specific crosscoupling compound and a specific catalyst for producing the compound. The method includes reacting in the presence of a base and a nickel compound catalyst organic halide of the formula n′(R 1 X 1 n ), wherein R 1 is a hydrocarbon group and the α and β carbons to X′ are sp 3 carbon atoms; X 1 is a chlorine, bromine, or iodine atoms, and n and n 1 are 1 or 2 but not both 2, with a compound having the formula mR 2 (BX 2 2 ) n′ } where an R 2 is an aryl, heteroaryl, or alkenyl group, and n′ is 1 or 2, X 2 is independently a hydroxyl group, an alkoxy or arylalkoxy group or X 2 2 together form an alkylenedioxy or arylenedioxy group, and m represents 1 or 2 but m≦n, and the boron atom is bonded to a sp 2 carbon atom of R 2 group or a boronic acid trimer anhydride.
    提供了一种生产特定交叉偶联化合物和特定催化剂以生产该化合物的方法。该方法包括在碱和镍化合物催化剂的存在下,将具有以下公式的有机卤化物n’(R1X1n)与具有以下公式的化合物m R2(BX22)n’}反应,其中R1是一个碳氢基团,α和β碳至X’是sp3碳原子;X1是氯、溴或碘原子,n和n1为1或2但不同时为2;R2是芳基、杂环芳基或烯基基团,n’为1或2,X2独立地是羟基、烷氧基或芳基烷氧基,或X22共同形成烷二酮基或芳二酮基;m表示1或2,但m≦n,硼原子与R2基团的sp2碳原子或硼酸三聚体酐键合。
  • POLYIMIDAZOLES FOR USE AS BILE ACID SEQUESTRANTS
    申请人:Lees Inez
    公开号:US20130189215A1
    公开(公告)日:2013-07-25
    The present invention provides crosslinked amine polymers effective for binding and removing bile salts from the gastrointestinal tract. These bile acid binding polymers or pharmaceutical compositions thereof can be administered to subjects to treat various conditions, including hypercholesteremia, diabetes, pruritus, irritable bowel syndrome-diarrhea (IBS-D), bile acid malabsorption, and the like.
    本发明提供了交联胺聚合物,可以有效地结合和清除胆汁酸从胃肠道中。这些胆酸结合聚合物或其制药组合物可以用于治疗各种疾病,包括高胆固醇血症,糖尿病,瘙痒,肠易激综合征-腹泻(IBS-D),胆酸吸收不良等。
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