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1,1,3,3,5,5,7,7,9,9-十甲基五硅氧烷 | 995-83-5

中文名称
1,1,3,3,5,5,7,7,9,9-十甲基五硅氧烷
中文别名
十甲基二氢五硅氧烷
英文名称
1,1,3,3,5,5,7,7,9,9-decamethylpentasiloxane
英文别名
Bis[[dimethylsilyloxy(dimethyl)silyl]oxy]-dimethylsilane
1,1,3,3,5,5,7,7,9,9-十甲基五硅氧烷化学式
CAS
995-83-5
化学式
C10H32O4Si5
mdl
——
分子量
356.789
InChiKey
OMABSGMMFGVCDF-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:
    100°C / 20
  • 密度:
    0.8818 g/cm3
  • 溶解度:
    苯(可溶)、氯仿(微量)

计算性质

  • 辛醇/水分配系数(LogP):
    3.13
  • 重原子数:
    19
  • 可旋转键数:
    8
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    36.9
  • 氢给体数:
    0
  • 氢受体数:
    4

安全信息

  • 包装等级:
    II
  • 危险类别:
    3
  • 危险性防范说明:
    P501,P240,P210,P233,P243,P241,P242,P280,P370+P378,P303+P361+P353,P403+P235
  • 危险品运输编号:
    1993
  • 危险性描述:
    H225
  • 储存条件:
    存储条件:2~8℃,干燥且密封。

SDS

SDS:fd7eaf6e5784b478e5d6546f487dc05e
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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

  • 作为反应物:
    描述:
    烯丙基丁基醚1,1,3,3,5,5,7,7,9,9-十甲基五硅氧烷 在 cis-bis(dibenzyl sulfide)Pt(II) dichloride 作用下, 以 二氯甲烷甲苯 为溶剂, 生成 1-(3-butoxypropyl)-1,1,3,3,5,5,7,7,9,9-decamethylpentasiloxane
    参考文献:
    名称:
    Spectral study of interaction between allyl ethers and hydrosiloxanes
    摘要:
    Interaction of allyl ethers with hydrosiloxanes in the presence of metal complexes has been investigated by spectral methods (H-1 NMR, IR, and GC-MS) as well as by gas-liquid chromatography. It has been shown that the anti-Markovnikov addition predominantly occurs in the studied cases; disproportionation of siloxanes and migration of double bond in the ethers have been identified as side reactions. The tendency to enter the side reactions has decreased in the following series: (HMeSiO)(4) > HMe2Si(OSiMe2)(2)H a parts per thousand HMe2SiOSiMe3 > (HMe2Si)(2)O > (Me3SiOSiMeH)(2)O. The general scheme of disproportionation of siloxanes HMe2Si(OSiMe2) (n) H (n a parts per thousand yen 1) has been proposed. According to mass spectrometry data, the silicon-containing fragment majorly contributes to the fragmentation of hydrosilylation products. Fragmentation of the gamma,gamma-adducts is similar to that of gamma-adducts. The predominant direction of fragmentation in the products of beta,gamma-addition of HMe2Si(OSiMe2)nH (n = 1-3) to allyl ethers is determined by fragmentation of the gamma-component of the molecule. The scheme of fragmentation of the hydrosilylation products ions has been proposed.
    DOI:
    10.1134/s1070363214010095
  • 作为产物:
    描述:
    二甲基一氯硅烷六甲基环三硅氧烷二氧化硫 作用下, 以 正己烷 为溶剂, 以73%的产率得到1,1,3,3,5,5,7,7,9,9-十甲基五硅氧烷
    参考文献:
    名称:
    A Convenient Synthesis of α,ω-Difunctionalized Linear Dimethylsiloxanes with Definite Chain Lengths
    摘要:
    α,ω-双官能化线性二甲基硅氧烷以明确的链长,通过在非常温和的条件下,使用无机固体催化剂催化环裂解环二甲基硅氧烷与二甲基氯硅烷和水的反应来便利地制备。
    DOI:
    10.1246/cl.1990.2133
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文献信息

  • COSMETIC
    申请人:SHIN-ETSU CHEMICAL CO., LTD.
    公开号:US20200281836A1
    公开(公告)日:2020-09-10
    A cosmetic containing (A) an organo(poly)siloxane shown by the following general formula (1). A cosmetic with a refreshing feeling, smooth spreadability as well as high stability and favorable cosmetic sustainability is provided. [where, in the formula, R 1 represents a group except shown by the formula (2), selected from a C1-C20 alkyl group and a C6-C20 aryl group; n represents an integer of 0 to 3; R 2 and R 3 represent R 1 or the formula (2); and either or both of R 2 and R 3 represent formula (2), (where, in the formula, X represents a C2-C20 alkylene group; and Y represents any one of a hydrogen atom, a C1-C20 alkyl group, a C6-C20 aryl group, a C7-C40 aralkyl group, a C1-C20 alkyloxy group, a C6-C20 aryloxy group, a C7-C40 arylalkyloxy group, and a halogen atom.)]
    一种化妆品,含有以下一般式(1)所示的有机(聚)硅氧烷。提供一种具有清爽感、平滑涂抹性以及高稳定性和良好的化妆品持久性的化妆品。【在公式中,R1代表除公式(2)所示之外的一种基团,选自C1-C20烷基基团和C6-C20芳基基团;n代表0到3之间的整数;R2和R3代表R1或公式(2);R2和R3中的任一或两者代表公式(2),(在公式中,X代表C2-C20烷基基团;Y代表氢原子、C1-C20烷基基团、C6-C20芳基基团、C7-C40芳基烷基基团、C1-C20烷氧基团、C6-C20芳氧基团、C7-C40芳基烷氧基团和卤素原子中的任意一种。)】
  • NOVEL LIQUID TETRACARBOXYLIC DIANHYDRIDES AND PROCESS FOR THE PREPARATION THEREOF
    申请人:Kikuchi Tooru
    公开号:US20110301362A1
    公开(公告)日:2011-12-08
    The invention relates to a tetracarboxylic dianhydride represented by the following formula (1). [In formula (1) R 1 , R 2 , R 3 and R 4 each independently represent an alkyl group having from 1 to 5 carbon atoms, m represents a number from 1 to 30, all of the silicon atoms bonding to the norbornane rings are in an exo-configuration with respect to the norbornane rings, and all of the dicarboxylic anhydride groups bonding to the norbornane rings are in an exo-configuration with respect to the norbornane rings.]
    该发明涉及一种由以下式(1)表示的四羧酐二酐。[在式(1)中,R1、R2、R3和R4分别独立表示由1到5个碳原子组成的烷基基团,m表示一个从1到30的数字,所有与去氢莰环结合的硅原子都是相对于去氢莰环处于外向构型,所有与去氢莰环结合的二羧酐基团都是相对于去氢莰环处于外向构型。]
  • Synthesis and properties of new dibenzoylmethanatoboron difluoride dyads connected by flexible siloxane linkers
    作者:Yuriy N. Kononevich、Anastasia S. Belova、Viacheslav A. Sazhnikov、Andrey A. Safonov、Dmitry S. Ionov、Alexander D. Volodin、Alexander A. Korlyukov、Aziz M. Muzafarov
    DOI:10.1016/j.tetlet.2020.152176
    日期:2020.7
    excimer formation) emissions are observed for the dyads in dilute dichloromethane solutions at room temperature. The excimers contribution into the total fluorescence spectrum decreases with increasing siloxane linker length. The parallel-sandwich conformation of intramolecular pre-excimers formed by two terminal DBMBF2 moieties is confirmed by DFT-based calculations.
    合成并表征了通过可变长度的柔性二甲基硅氧烷接头连接的一系列新颖的二苯甲酰甲基氨基硼酸二氟化物(DBMBF 2)和甲氧基取代的DBMBF 2二联体。在室温下,在稀释的二氯甲烷溶液中观察到二元组的单体和准分子(低分子内准分子的形成)发射。准分子对总荧光光谱的贡献随着硅氧烷接头长度的增加而降低。通过基于DFT的计算证实了由两个末端DBMBF 2部分形成的分子内准分子的平行夹心构象。
  • METHOF FOR PRODUCING HYDRIDOSILANES
    申请人:WACKER CHEMIE AG
    公开号:US20190345175A1
    公开(公告)日:2019-11-14
    The invention relates to a method for producing hydridosilanes, in which siloxanes containing Si—H groups are reacted in the presence of a cationic Si(II) compound as a catalyst.
    这项发明涉及一种生产氢硅烷的方法,其中含有Si-H基团的硅氧烷在阳离子Si(II)化合物存在下作为催化剂进行反应。
  • Effect of catalyst structure on the reaction of α-methylstyrene with 1,1,3,3-tetramethyldisiloxane
    作者:D. A. de Vekki、N. K. Skvortsov
    DOI:10.1134/s107036320904015x
    日期:2009.4
    Reaction of α-methylstyrene with 1,1,3,3-tetramethyldisiloxane in the presence of the complexes of platinum(II), palladium(II) and rhodium(I) is explored. It is established that in the presence of platinum catalyst predominantly occurs hydrosilylation of α-methylstyrene leading to formation of β-adduct, on palladium catalysts proceeds reduction of α-methylstyrene, on rhodium catalysts both the processes
    探索了在铂(II),钯(II)和铑(I)的络合物存在下α-甲基苯乙烯与1,1,3,3-四甲基二硅氧烷的反应。已经确定在铂催化剂的存在下主要发生α-甲基苯乙烯的氢化硅烷化,导致形成β-加合物,在钯催化剂上进行α-甲基苯乙烯的还原,在铑催化剂上这两种方法均发生。在反应混合物中,发生1,1,3,3-四甲基二硅氧烷的歧化和脱氢缩合反应,导致形成通式为HMe 2 Si(OSiMe 2)n H和(-OSiMe 2-)m(n = 2–6,m = 3–7)。铂催化剂促进线性硅氧烷的形成,而铑和钯催化剂也提供线性和环状硅氧烷。研究了中间金属配合物的结构。
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同类化合物

(2-溴乙氧基)-特丁基二甲基硅烷 骨化醇杂质DCP 马来酸双(三甲硅烷)酯 顺式-二氯二(二甲基硒醚)铂(II) 顺-N-(1-(2-乙氧基乙基)-3-甲基-4-哌啶基)-N-苯基苯酰胺 降钙素杂质13 降冰片烯基乙基三甲氧基硅烷 降冰片烯基乙基-POSS 间-氨基苯基三甲氧基硅烷 镁,氯[[二甲基(1-甲基乙氧基)甲硅烷基]甲基]- 锑,二溴三丁基- 铷,[三(三甲基甲硅烷基)甲基]- 铂(0)-1,3-二乙烯-1,1,3,3-四甲基二硅氧烷 钾(4-{[二甲基(2-甲基-2-丙基)硅烷基]氧基}-1-丁炔-1-基)(三氟)硼酸酯(1-) 金刚烷基乙基三氯硅烷 辛醛,8-[[(1,1-二甲基乙基)二甲基甲硅烷基]氧代]- 辛甲基-1,4-二氧杂-2,3,5,6-四硅杂环己烷 辛基铵甲烷砷酸盐 辛基衍生化硅胶(C8)ZORBAX?LP100/40C8 辛基硅三醇 辛基甲基二乙氧基硅烷 辛基三甲氧基硅烷 辛基三氯硅烷 辛基(三苯基)硅烷 辛乙基三硅氧烷 路易氏剂-3 路易氏剂-2 路易士剂 试剂3-[Tris(trimethylsiloxy)silyl]propylvinylcarbamate 试剂2-(Trimethylsilyl)cyclopent-2-en-1-one 试剂11-Azidoundecyltriethoxysilane 西甲硅油杂质14 衣康酸二(三甲基硅基)酯 苯胺,4-[2-(三乙氧基甲硅烷基)乙基]- 苯磺酸,羟基-,盐,单钠聚合甲醛,1,3,5-三嗪-2,4,6-三胺和脲 苯甲醇,a-[(三苯代甲硅烷基)甲基]- 苯基二甲基氯硅烷 苯基二甲基乙氧基硅 苯基乙酰氧基三甲基硅烷 苯基三辛基硅烷 苯基三甲氧基硅烷 苯基三乙氧基硅烷 苯基三丁酮肟基硅烷 苯基三(异丙烯氧基)硅烷 苯基三(2,2,2-三氟乙氧基)硅烷 苯基(3-氯丙基)二氯硅烷 苯基(1-哌啶基)甲硫酮 苯乙基三苯基硅烷 苯丙基乙基聚甲基硅氧烷 苯-1,3,5-三基三(三甲基硅烷)