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Chlormethyl-isopropyl-sulfid | 18267-19-1

中文名称
——
中文别名
——
英文名称
Chlormethyl-isopropyl-sulfid
英文别名
2-Chloromethylsulfanyl-propane;2-(chloromethylsulfanyl)propane
Chlormethyl-isopropyl-sulfid化学式
CAS
18267-19-1
化学式
C4H9ClS
mdl
——
分子量
124.634
InChiKey
GTGKNQUHLOGQGH-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):
    2.4
  • 重原子数:
    6
  • 可旋转键数:
    2
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    25.3
  • 氢给体数:
    0
  • 氢受体数:
    1

SDS

SDS:db5f317aa871c79caf57f21319dda61b
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反应信息

  • 作为反应物:
    参考文献:
    名称:
    Sigma-Halo sulfones. XI. Ramberg-Backlund rearrangement of trichloromethyl sulfones
    摘要:
    DOI:
    10.1021/ja01026a040
  • 作为产物:
    参考文献:
    名称:
    BROWN, JONATHAN M.;CHRISTODOULOU, CHRIS;JONES, SIMON S.;MODAK, ANIL S.;RE+, J. CHEM. SOC. PERKIN TRANS. PT 1,(1989) N0, C. 1735-1750
    摘要:
    DOI:
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文献信息

  • [EN] INHIBITORS OF SHORT-CHAIN DEHYDROGENASE ACTIVITY FOR TREATING FIBROSIS<br/>[FR] INHIBITEURS DE L'ACTIVITÉ DE LA DÉSHYDROGÉNASE À CHAÎNE COURTE POUR LE TRAITEMENT DE LA FIBROSE
    申请人:UNIV CASE WESTERN RESERVE
    公开号:WO2016144958A1
    公开(公告)日:2016-09-15
    A method of treating or preventing a fibrotic disease, disorder or condition includes administering to a subject in need of treatment a 15-PGDH inhibitor.
    治疗或预防纤维化疾病、紊乱或状况的方法包括向需要治疗的对象施用15-PGDH抑制剂。
  • [EN] INHIBITORS OF SHORT-CHAIN DEHYDROGENASE ACTIVITY FOR PROMOTING NEUROGENESIS AND INHIBITING NERVE CELL DEATH<br/>[FR] INHIBITEURS DE L'ACTIVITÉ DÉSHYDROGÉNASE À CHAÎNE COURTE POUR FAVORISER LA NEUROGENÈSE ET INHIBER LA MORT DES CELLULES NERVEUSES
    申请人:UNIV CASE WESTERN RESERVE
    公开号:WO2018017582A1
    公开(公告)日:2018-01-25
    A method of promoting neuroprotection in a subject from axonal degeneration, neuronal cell death, and/or glia cell damage after injury, augmenting neuronal signaling underlying learning and memory, stimulating neuronal regeneration after injury, and/or treating a disease, disorder, and/or condition of the nervous system in a subject in need thereof includes administering to the subject a therapeutically effective amount of a 15-PGDH inhibitor.
    在需要的受试者中,促进神经保护的方法包括向受试者施用治疗有效量的15-PGDH抑制剂,以防止轴突退化、神经细胞死亡和/或胶质细胞损伤,增强学习和记忆的神经信号传导,刺激受伤后的神经再生,以及/或治疗神经系统的疾病、紊乱和/或状况。
  • Selective caspase inhibitors and uses thereof
    申请人:Genesis Technologies Limited
    公开号:US09562069B2
    公开(公告)日:2017-02-07
    The present invention relates to compounds of Formula I, IA, II, HA, III, or IHA and their pharmaceutical uses. Particular aspects of the invention relate to the use of those compounds for the selective inhibition of one or more caspases. Also described are methods where the compounds of Formula I, IA, II, IIA, III, or IIIA are used in the prevention and/or treatment of various diseases and conditions in subjects, including caspase-mediated diseases such as sepsis, myocardial infarction, ischemic stroke, spinal cord injury (SCI), traumatic brain injury (TBI) and neurodegenerative disease (e.g. multiple sclerosis (MS) and Alzheimer's, Parkinson's, and Huntington's diseases).
    本发明涉及式I、IA、II、HA、III或IHA的化合物及其药用用途。该发明的特定方面涉及利用这些化合物对一个或多个半胱氨酸蛋白酶进行选择性抑制。还描述了一些方法,其中式I、IA、II、IIA、III或IIIA的化合物用于预防和/或治疗受试者中的各种疾病和病况,包括半胱氨酸蛋白酶介导的疾病,如败血症、心肌梗死、缺血性中风、脊髓损伤(SCI)、创伤性脑损伤(TBI)和神经退行性疾病(如多发性硬化症(MS)以及阿尔茨海默病、帕金森病和亨廷顿病)。
  • The Generation of the Ethenethiolate Anion and Its Reaction with Several Chloromethyl Alkyl Ethers and Sulfides
    作者:Shigeo Tanimoto、Hideyuki Ikehira、Tatsuo Oida、Toshio Kokubo
    DOI:10.1246/bcsj.56.1261
    日期:1983.4
    3-oxathiolane was deprotonated at the 4-position, followed by the cycloelimination of the resultant anion, leading to ethyl formate and the ethenethiolate anion. The anion was trapped by several chloromethyl alkyl ethers and sulfides to afford alkoxy(vinylthio)methanes and alkylthio(vinylthio)methanes respectively.
    2-Ethoxy-1,3-oxathiolane 在 4-位被去质子化,随后生成的阴离子环消,生成甲酸乙酯和乙烯硫醇阴离子。阴离子被几种氯甲基烷基醚和硫化物捕获,分别得到烷氧基(乙烯基硫代)甲烷和烷硫基(乙烯基硫代)甲烷。
  • Chlorination of unsymmetrical sulfides
    作者:David L. Tuleen、Thomas Stephens
    DOI:10.1021/jo00838a009
    日期:1969.1
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