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N-(t-Butylthio)piperidin | 3060-70-6

中文名称
——
中文别名
——
英文名称
N-(t-Butylthio)piperidin
英文别名
N-tert.-Butylthio-piperidin;1-tert-butylsulfanyl-piperidine;1-(2-methyl-propane-2-sulfenyl)-piperidine;1-(2-Methyl-propan-2-sulfenyl)-piperidin;1-Tert-butylsulfanylpiperidine;1-tert-butylsulfanylpiperidine
N-(t-Butylthio)piperidin化学式
CAS
3060-70-6
化学式
C9H19NS
mdl
——
分子量
173.323
InChiKey
XTKKASUSYNBHAN-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):
    2.5
  • 重原子数:
    11
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    28.5
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    描述:
    N-(t-Butylthio)piperidin4-碘苯甲醚 、 ammonium acetate 、 四丁基醋酸铵 、 tert-butylammonium hexafluorophosphate(V) 作用下, 以 甲醇 为溶剂, 以65%的产率得到1-(S-tert-butylsulfonimidoyl)piperidine
    参考文献:
    名称:
    通过阳极生成的高价碘中间体电化学氧化合成 NH-Sulfoximines、NH-Sulfonimidamides 和 Dibenzothiazines
    摘要:
    在此,我们报告了一种通过直接电化学氧化催化合成 NH-亚砜亚胺和 NH-磺酰亚胺酰胺的通用方法,该催化涉及碘芳烃 (I)/碘芳烃 (III) 氧化还原对。此外,二苯并噻嗪可以在标准条件下由 [1,1'-联芳基]-2-硫化物合成。值得注意的是,原位生成活性高价碘催化剂只需要催化量的碘芳烃,这避免了相对于常规方法需要过量的高价碘试剂。此外,该协议具有广泛的底物范围和广泛的官能团耐受性,即使在超过 10 g 的规模下,也能以良好到卓越的收率交付目标化合物。
    DOI:
    10.1002/cssc.202101002
  • 作为产物:
    参考文献:
    名称:
    Peyron; Laplaine, Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences, 1948, vol. 227, p. 132
    摘要:
    DOI:
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文献信息

  • Endovascular Treatment of a Lenticulostriate Artery Aneurysm with N-butyl Cyanoacrylate
    作者:Ramiro Larrazabal、David Pelz、J. Max Findlay
    DOI:10.1017/s0317167100001426
    日期:2001.8
    Background:

    Aneurysms arising from lenticulostriate artery branches in moyamoya-type disease are challenging lesions to treat, due to their fragility and deep location. Surgery is difficult and endovascular options may be limited.

    Methods:

    A 57-year-old woman presented with a right ganglionic parenchymal hemorrhage due to a ruptured lenticulostriate artery aneurysm associated with ipsilateral middle cerebral artery occlusion. The aneurysm and parent feeding artery were occluded using endovascular injection of N-butyl cyanoacrylate.

    Results:

    The aneurysm was successfully obliterated and although some glue did enter the more distal middle cerebral artery, there was no change in the patient's neurologic status.

    Conclusion:

    In highly selected cases where lenticulostriate aneurysms cannot be directly accessed for surgery or endovascular coiling, obliteration with liquid acrylic glue may be considered as a therapeutic option.

    背景:在莫亚莫亚型疾病中,由皮孔状动脉分支产生的动脉瘤因其脆性和深部位置,治疗起来具有挑战性。方法:一名 57 岁的女性因枕叶动脉动脉瘤破裂导致右侧神经节实质出血,并伴有同侧大脑中动脉闭塞。结果:动脉瘤被成功堵塞,虽然一些胶水进入了较远端大脑中动脉,但患者的神经状况没有发生变化。结论:在无法直接进入皮孔状动脉瘤进行手术或血管内卷曲的高选择性病例中,可以考虑使用液态丙烯酸胶水堵塞动脉瘤作为一种治疗选择。
  • Alkyl thiosulfenamides and process of producing them
    申请人:PHILLIPS PETROLEUM CO
    公开号:US02807615A1
    公开(公告)日:1957-09-24
  • Production of sulfenamides
    申请人:PHILLIPS PETROLEUM CO
    公开号:US02520400A1
    公开(公告)日:1950-08-29
  • [EN] OLIGONUCLEOTIDE COMPOSITIONS AND METHODS THEREOF<br/>[FR] COMPOSITIONS D'OLIGONUCLÉOTIDES ET MÉTHODES ASSOCIÉES
    申请人:WAVE LIFE SCIENCES LTD
    公开号:WO2018067973A1
    公开(公告)日:2018-04-12
    Among other things, the present disclosure relates to designed oligonucleotides, compositions, and methods thereof. In some embodiments, provided oligonucleotide compositions provide altered splicing of a transcript. In some embodiments, provided oligonucleotide compositions have low toxicity. In some embodiments, provided oligonucleotide compositions provide improved protein binding profiles. In some embodiments, provided oligonucleotide compositions have improved delivery. In some embodiments, provided oligonucleotide compositions have improved uptake. In some embodiments, the present disclosure provides methods for treatment of diseases using provided oligonucleotide compositions.
  • Electrochemical Oxidative Syntheses of NH‐Sulfoximines, NH‐Sulfonimidamides and Dibenzothiazines via Anodically Generated Hypervalent Iodine Intermediates
    作者:Xianqiang Kong、Long Lin、Xiaohui Chen、Yiyi Chen、Wei Wang、Bo Xu
    DOI:10.1002/cssc.202101002
    日期:2021.8.23
    through direct electrochemical oxidative catalysis involving an iodoarene(I)/iodoarene(III) redox couple. In addition, dibenzothiazines can be synthesized from [1,1′-biaryl]-2-sulfides under standard conditions. Notably, only a catalytic amount of iodoarene is required for the generation in situ of an active hypervalent iodine catalyst, which avoids the need for an excess of a hypervalent iodine reagent
    在此,我们报告了一种通过直接电化学氧化催化合成 NH-亚砜亚胺和 NH-磺酰亚胺酰胺的通用方法,该催化涉及碘芳烃 (I)/碘芳烃 (III) 氧化还原对。此外,二苯并噻嗪可以在标准条件下由 [1,1'-联芳基]-2-硫化物合成。值得注意的是,原位生成活性高价碘催化剂只需要催化量的碘芳烃,这避免了相对于常规方法需要过量的高价碘试剂。此外,该协议具有广泛的底物范围和广泛的官能团耐受性,即使在超过 10 g 的规模下,也能以良好到卓越的收率交付目标化合物。
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