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tert-butylhexyl disulfide | 64580-59-2

中文名称
——
中文别名
——
英文名称
tert-butylhexyl disulfide
英文别名
tert-butyl 1-hexyl disulfide;tert-butyl-hexyl-disulfane;1-(tert-Butyldisulfanyl)hexane
tert-butylhexyl disulfide化学式
CAS
64580-59-2
化学式
C10H22S2
mdl
——
分子量
206.417
InChiKey
HXFQCKLJIPUIKX-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:
    74-76 °C(Press: 0.1 Torr)
  • 密度:
    0.9560 g/cm3

计算性质

  • 辛醇/水分配系数(LogP):
    4.2
  • 重原子数:
    12
  • 可旋转键数:
    7
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    50.6
  • 氢给体数:
    0
  • 氢受体数:
    2

SDS

SDS:a78c238e45e7e7968c35a789dcd2e6f2
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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

  • 作为产物:
    描述:
    1-己硫醇 以30%的产率得到
    参考文献:
    名称:
    KULIEV A. B.; ZEJNALOVA G. A.; GASANOV M. S.; ALIEV F. YU., ZH. ORGAN. XIMII, 1978, 14, HO 3, 661
    摘要:
    DOI:
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文献信息

  • [EN] POLYNUCLEOTIDE CONSTRUCTS HAVING DISULFIDE GROUPS<br/>[FR] CONSTRUCTIONS POLYNUCLÉOTIDIQUES CONTENANT DES GROUPES DISULFURE
    申请人:SOLSTICE BIOLOG LTD
    公开号:WO2015069932A1
    公开(公告)日:2015-05-14
    The invention features polynucleotide constructs containing one or more components (i) containing a disulfide linkage, where each of the one or more components is attached to an internudeotide bridging group or a terminal group of the polynucleotide construct, and each of the one or more components (i) contains one or more bulky groups proximal to the disulfide group. The invention also features polynucleotide constructs containing one or more components (i) containing a disulfide linkage, where each of the one or more components (i) is attached to an internudeotide bridging group or a terminal group of the polynucleotide construct, and each of the one or more components (i) contains at least 4 atoms in a chain between the disulfide linkage and the phosphorus atom of the internudeotide bridging group or the terminal group; and where the chain does not contain a phosphate, an amide, an ester, or an alkenylene. The invention also features methods of delivering a polynucleotide to a cell using the polynucleotide constructs of the invention.
    该发明涉及包含一个或多个组分(i)的聚核苷酸构造,其中每个一个或多个组分连接到聚核苷酸构造的一个核苷酸桥连基团或末端基团上,每个一个或多个组分(i)包含靠近二硫键的一个或多个臃肿基团。该发明还涉及包含一个或多个组分(i)的聚核苷酸构造,其中每个一个或多个组分(i)连接到聚核苷酸构造的一个核苷酸桥连基团或末端基团上,每个一个或多个组分(i)在二硫键和核苷酸桥连基团或末端基团的磷原子之间的链中至少包含4个原子;并且该链不包含磷酸酯、酰胺、酯或烯基烃。该发明还涉及使用该发明的聚核苷酸构造将聚核苷酸传递到细胞的方法。
  • One-pot synthesis of unsymmetrical disulfides using 1-chlorobenzotriazole as oxidant: Interception of the sulfenyl chloride intermediate
    作者:Nashia Stellenboom、Roger Hunter、Mino R. Caira
    DOI:10.1016/j.tet.2010.02.077
    日期:2010.4
    is described for unsymmetrical disulfide synthesis from two different thiols using 1-chlorobenzotriazole (BtCl) as oxidant. The mechanism of the coupling involves in situ trapping of the sulfenyl chloride intermediate R1SCl by nucleophilic benzotriazole (BtH) to form R1SBt, which protects R1SCl from forming the homodimer R1SSR1. The methodology is applicable to all types of thiol (aliphatic, aromatic
    描述了一种高产,低温的一锅法,用于使用1-氯苯并三唑(BtCl)作为氧化剂由两种不同的硫醇合成不对称的二硫键。偶联的机制包括通过亲核苯并三唑(BtH)原位捕获亚磺酰氯中间体R 1 SCl形成R 1 SBt,从而保护R 1 SCl避免形成同型二聚体R 1 SSR 1。该方法适用于所有类型的硫醇(脂族,芳族,杂芳族),并为脂族-脂族偶联开发了一种变体。差异性的N-保护的半胱氨酸偶合,以高收率(90%)提供不对称的胱氨酸衍生物,该模型可作为含半胱氨酸的肽单分子间偶联形成肽二硫键异二聚体的模型。由于条件温和,因此注意到芳香族-芳香族二硫化物合成中的交换最少。
  • POLYNUCLEOTIDE CONSTRUCTS HAVING DISULFIDE GROUPS
    申请人:BRADSHAW Curt W.
    公开号:US20160257961A1
    公开(公告)日:2016-09-08
    The invention features polynucleotide constructs containing one or more components (i) containing a disulfide linkage, where each of the one or more components is attached to an internucleotide bridging group or a terminal group of the polynucleotide construct, and each of the one or more components (i) contains one or more bulky groups proximal to the disulfide group. The invention also features polynucleotide constructs containing one or more components (i) containing a disulfide linkage, where each of the one or more components (i) is attached to an internucleotide bridging group or a terminal group of the polynucleotide construct, and each of the one or more components (i) contains at least 4 atoms in a chain between the disulfide linkage and the phosphorus atom of the internucleotide bridging group or the terminal group; and where the chain does not contain a phosphate, an amide, an ester, or an alkenylene. The invention also features methods of delivering a polynucleotide to a cell using the polynucleotide constructs of the invention.
    本发明涉及一种聚核苷酸构建物,其包含一个或多个组分(i),该组分包含一个二硫键,其中每个组分中的一个或多个组分连接到聚核苷酸构建物的核苷酸桥接基团或末端基团上,并且每个组分(i)在二硫键附近包含一个或多个笨重基团。本发明还涉及一种聚核苷酸构建物,其包含一个或多个组分(i),该组分包含一个二硫键,其中每个组分中的一个或多个组分连接到聚核苷酸构建物的核苷酸桥接基团或末端基团上,并且每个组分(i)在二硫键和核苷酸桥接基团或末端基团的磷原子之间的链中至少含有4个原子;并且链中不含有磷酸盐、酰胺、酯或烯基烃。本发明还涉及使用本发明的聚核苷酸构建物向细胞传递聚核苷酸的方法。
  • Singh, Sundaram; Singh, Manorama; Singh, Krishna Nand, Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry, 1998, vol. 37, # 3-4, p. 411 - 414
    作者:Singh, Sundaram、Singh, Manorama、Singh, Krishna Nand
    DOI:——
    日期:——
  • The Regioselective Reaction of Atomic Hydrogen with Unsymmetric Disulfides and Sulfides
    作者:Dennis D. Tanner、Liying Zhang、Markandu Vigneswaran、Pramod Kandanarachchi
    DOI:10.1021/jo00119a027
    日期:1995.7
    Unsymmetric disulfides undergo solution phase reduction with atomic hydrogen regioselectively by displacement at the least hindered sulfur atom. The cleavage of the sulfur-sulfur bond forms mixtures of two thiol and two thiyl radicals. At the temperature at which the reactions are carried out, the thiyl radicals form symmetric disulfides by thiyl-thiyl radical coupling and not by thiyl radical displacement on the starting material. The reaction of atomic hydrogen with an unsymmetric sulfide is a cleavage that favors the formation of the most stable radical. The reaction of phenyl cyclohexyl sulfide produces benzene, cyclohexane, cyclohexyl thiol, and thiophenol. Benzene and cyclohexyl thiol produced from the cleavage of the phenyl-sulfur bond are proposed to arise from the ct-scission of an intermediate formed by ipso-addition of atomic hydrogen to the benzene ring.
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