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1-bromo-3-phenylsulfanylpropan-2-ol | 104792-76-9

中文名称
——
中文别名
——
英文名称
1-bromo-3-phenylsulfanylpropan-2-ol
英文别名
1-bromo-3-(phenylthio)propan-2-ol;1-Bromo-3-phenylthio-propan-2-ol
1-bromo-3-phenylsulfanylpropan-2-ol化学式
CAS
104792-76-9
化学式
C9H11BrOS
mdl
——
分子量
247.156
InChiKey
ZEPKHMNDIHKITL-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):
    2.6
  • 重原子数:
    12
  • 可旋转键数:
    4
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.33
  • 拓扑面积:
    45.5
  • 氢给体数:
    1
  • 氢受体数:
    2

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:
    1-bromo-3-phenylsulfanylpropan-2-ol三乙胺 作用下, 以 乙醚丙酮 为溶剂, 反应 2.03h, 生成 (4-Chlorophenyl) 2-oxo-5-(phenylsulfanylmethyl)-1,3-oxazolidine-3-sulfonate
    参考文献:
    名称:
    Formation of N‐Sulfonylcarbamates from Epichlorohydrin: Synthesis of Polyfunctional Oxazolidin‐2‐ones
    摘要:
    DOI:
    10.1080/00397910701396922
  • 作为产物:
    描述:
    1,3-二溴-2-丙醇苯硫酚三乙胺 作用下, 以 二氯甲烷 为溶剂, 反应 72.0h, 以73%的产率得到1-bromo-3-phenylsulfanylpropan-2-ol
    参考文献:
    名称:
    [EN] SUBSTITUTED MONO- AND POLY-PHENYL-CORE MONOMERS AND POLYMERS THEREOF FOR VOLUME BRAGG GRATINGS
    [FR] MONOMÈRES À NOYAUX MONOPHÉNYLE ET POLYPHÉNYLE SUBSTITUÉS ET LEURS POLYMÈRES POUR RÉSEAUX DE BRAGG EN VOLUME
    摘要:
    本公开提供了用于体积布拉格光栅的单核苯基或多核苯基衍生单体和聚合物的记录材料,包括但不限于用于全息应用的体积布拉格光栅。公开了用于布拉格光栅应用的单核苯基或多核苯基衍生单体和聚合物的几种结构,导致具有更高的折射率,低双折射率和高透明度的材料。公开的单核苯基或多核苯基衍生单体和聚合物可以用于任何体积布拉格光栅材料,包括两阶段聚合物材料,其中基质在第一步中固化,然后通过第二次单体固化步骤编写体积布拉格光栅。
    公开号:
    WO2022104113A1
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文献信息

  • AROMATIC SUBSTITUTED ALKANE-CORE MONOMERS AND POLYMERS THEREOF FOR VOLUME BRAGG GRATINGS
    申请人:Facebook Technologies, LLC
    公开号:US20210155599A1
    公开(公告)日:2021-05-27
    The disclosure provides recording materials including aromatic substituted alkane-core derivatized monomers and polymers for use in volume Bragg gratings, including, but not limited to, volume Bragg gratings for holography applications. Several structures are disclosed, including Formula I. When used in Bragg gratings applications, the monomers and polymers disclosed lead to materials with higher refractive index, low birefringence, and high transparency. The disclosed derivatized monomers and polymers can be used in any volume Bragg gratings materials, including two-stage polymer materials where a matrix is cured in a first step, and then the volume Bragg grating is written by way of a second curing step of a monomer.
    披露提供了包括芳香取代烷基核衍生单体和聚合物在内的记录材料,用于体积布拉格光栅,包括但不限于用于全息应用的体积布拉格光栅。披露了几种结构,包括式I。当在布拉格光栅应用中使用时,披露的单体和聚合物导致具有较高折射率、低双折射和高透明度的材料。披露的衍生单体和聚合物可用于任何体积布拉格光栅材料,包括两阶段聚合物材料,其中矩阵在第一步中固化,然后通过单体的第二次固化步骤编写布拉格光栅。
  • Fungicidal 2-substituted-1-(1-imidazolyl)-propyl aryl sulfides,
    申请人:Chevron Research Company
    公开号:US04602030A1
    公开(公告)日:1986-07-22
    Compounds of the formula: ##STR1## wherein n is 0, 1 or 2; R.sup.1 is phenyl optionally substituted with 1 to 5 substitutents independently selected from halogen, lower alkyl, lower alkoxy, nitro, cyano, lower carbalkoxy or amino optionally substituted with 1 or 2 lower alkyl groups; and Y is hydroxy; halogen; --OCH.sub.2 R.sup.2 wherein R.sup.2 is lower alkyl, or lower alkenyl optionally substituted with 1 to 5 halogen atoms, or phenyl optionally substituted with 1 to 5 substituents independently selected from halogen, lower alkyl, nitro, lower alkoxy, cyano or lower carbalkoxy; ##STR2## wherein R.sup.3 is phenyl optionally substituted with 1 to 5 substituents independently selected from halogen, lower alkoxy, or nitro, are active as fungicides.
    该化合物的公式为:其中n为0、1或2;R.sup.1为苯基,可选择地取代为1至5个卤素、低烷基、低烷氧基、硝基、氰基、低碳酰氧基或氨基,可选择地取代为1或2个低烷基基团;Y为羟基;卤素;--OCH.sub.2 R.sup.2,其中R.sup.2为低烷基,或可选择地取代为1至5个卤素原子的低烯基,或苯基,可选择地取代为1至5个卤素、低烷基、硝基、低烷氧基、氰基或低碳酰氧基的基团;其中R.sup.3为苯基,可选择地取代为1至5个卤素、低烷氧基或硝基的基团,具有杀菌剂活性。
  • Complex catalyst, process for producing the complex catalyst, and process for producing alchohol derivative with the complex catalyst
    申请人:——
    公开号:US20040077487A1
    公开(公告)日:2004-04-22
    There are provided (asymmetric) complex catalysts comprising metal complexes and Lewis acids as components, the metal complex being of formula (1): 1 wherein R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 and R 8 are the same or different and are independently hydrogen, halogen, alkyl or the like; one of R 9 and R 10 is hydrogen and the other is alkyl of 1 to 4 carbon atoms or the like; Q is a single bond or alkylene of 1 to 4 carbon atoms; M is a metal ion; and A is a balancing counter ion or ligand; processes for the production of these complex catalysts; processes for the production of (optically active) alcohol derivatives, characterized in that cyclic ether compounds are reacted with phenol derivatives in the presence of these complex catalysts; and further processes for producing (optically active) nitrogen-containing heterocyclic compounds by reacting these alcohol derivatives with halogenated nitrogen-containing heterocyclic compounds in the presence of a base.
    提供了由金属配合物和路易斯酸组成的(不对称的)复杂催化剂,其中金属配合物的化学式为(1):1其中R1、R2、R3、R4、R5、R6、R7和R8相同或不同,独立地是氢、卤素、烷基或类似物;R9和R10中的一个是氢,另一个是1至4个碳原子的烷基或类似物;Q是单键或1至4个碳原子的烷基;M是金属离子;A是平衡的反离子或配体;制备这些复杂催化剂的方法;制备(光学活性的)醇衍生物的方法,其特征在于在这些复杂催化剂的存在下,环氧化合物与酚衍生物反应;以及在碱的存在下,通过将这些醇衍生物与卤素化的含氮杂环化合物反应,制备(光学活性的)含氮杂环化合物的进一步方法。
  • [EN] SUBSTITUTED PROPANE-CORE MONOMERS AND POLYMERS THEREOF FOR VOLUME BRAGG GRATINGS<br/>[FR] MONOMÈRES À NOYAUX DE TYPE PROPANE SUBSTITUÉS ET LEURS POLYMÈRES POUR RÉSEAUX DE BRAGG EN VOLUME
    申请人:FACEBOOK TECH LLC
    公开号:WO2022104137A1
    公开(公告)日:2022-05-19
    The disclosure provides recording materials including propane derivatized monomers and polymers for use in volume Bragg gratings, including, but not limited to, volume Bragg gratings for holography applications. Several structures are disclosed for propane derivatized monomers and polymers for use in Bragg gratings applications, leading to materials with higher refractive index, low birefringence, and high transparency. The disclosed propane derivatized monomers and polymers thereof can be used in any volume Bragg gratings materials, including two-stage polymer materials where a matrix is cured in a first step, and then the volume Bragg grating is written by way of a second curing step of a monomer.
    本公开提供了包括丙烷衍生单体和聚合物的记录材料,用于体积布拉格光栅,包括但不限于用于全息学应用的体积布拉格光栅。本公开揭示了用于布拉格光栅应用的丙烷衍生单体和聚合物的几种结构,导致具有较高折射率、低双折射和高透明度的材料。所披露的丙烷衍生单体和聚合物可以用于任何体积布拉格光栅材料中,包括两阶段聚合物材料,其中矩阵在第一步中固化,然后通过单体的第二次固化步骤写入体积布拉格光栅。
  • METHOD FOR PRODUCING OPTICALLY ACTIVE ALCOHOL COMPOUND
    申请人:Sumitomo Chemical Company, Limited
    公开号:EP1982972A1
    公开(公告)日:2008-10-22
    A method for producing an optically active alcohol compound comprising reacting a cyclic ether compound with a phenol compound in the presence of an asymmetric complex obtained by reacting an optically active metal complex represented by the formula (1): wherein R1, R2, R3, R4, R5, R6, R7 and R8 are the same or different and each independently represent a hydrogen atom, an alkyl group or the like; one of R9 and R10 is a hydrogen group and the other is a substituted or unsubstituted phenyl group or the like; Q represents a single bond, a C1-C4 alkylene group or the like; M represents a metal ion; and when an ionic valency of the metal ion is same as a coordination number of a ligand, A is nonexistent, and when the above-mentioned ionic valency is different from the coordination number, and A represents a counter ion or a ligand, with a zirconium alkoxide or a hafnium alkoxide.
    一种生产光学活性醇化合物的方法,包括在由式(1)表示的光学活性金属络合物反应得到的不对称络合物存在下,使环醚化合物与苯酚化合物反应: 其中 R1、R2、R3、R4、R5、R6、R7 和 R8 相同或不同,且各自独立地代表氢原子、烷基或类似基团; R9 和 R10 中的一个是氢基,另一个是取代或未取代的苯基或类似基团; Q 代表单键、C1-C4 亚烷基或类似物; M 代表金属离子;当金属离子的离子价与配体的配位数相同时,A 不存在,当上述离子价与配位数不同时,A 代表金属离子。 当上述离子价与配位数不同,且 A 代表反离子或配体时,用氧化锆或氧化铪。
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