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2-羟基乙基戊基硫化物 | 22812-91-5

中文名称
2-羟基乙基戊基硫化物
中文别名
——
英文名称
(2-Hydroxyethyl)-pentylsulfid
英文别名
Amyl-β-hydroxy-aethylsulfid;2-Pentylthioethanol;2-pentylsulfanyl-ethanol;Amyl 2-hydroxyethyl sulfide;2-pentylsulfanylethanol
2-羟基乙基戊基硫化物化学式
CAS
22812-91-5
化学式
C7H16OS
mdl
MFCD00014043
分子量
148.269
InChiKey
GMCYCIFSAJJFSY-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
  • 重原子数:
    9
  • 可旋转键数:
    6
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    45.5
  • 氢给体数:
    1
  • 氢受体数:
    2

安全信息

  • 海关编码:
    2930909090

SDS

SDS:d47b15fc89e39a044982a04a8fd7fbad
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反应信息

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文献信息

  • POLY(PHOSPHOESTERS) FOR DELIVERY OF NUCLEIC ACIDS
    申请人:TRANSLATE BIO, INC.
    公开号:US20200277446A1
    公开(公告)日:2020-09-03
    Disclosed are polymers comprising the moiety A, which is a moiety of formula I: and pharmaceutically acceptable salts thereof, wherein R, R 1 , R 2 , L, n1 and n2 are as defined herein. These polymers are useful for delivering nucleic acids to subject. These polymers and pharmaceutically acceptable compositions comprising such polymers and nucleic acids can be useful for treating various diseases, disorders and conditions.
    揭示了包含A基团的聚合物,该基团是化学式I的基团:及其药用可接受的盐,其中R、R1、R2、L、n1和n2如本文所定义。这些聚合物对于将核酸传递给受试者是有用的。这些聚合物和包含这些聚合物和核酸的药用可接受组合物可用于治疗各种疾病、疾病和症状。
  • [EN] HCV POLYMERASE INHIBITORS<br/>[FR] INHIBITEURS DE LA POLYMÉRASE DU VHC
    申请人:MEDIVIR AB
    公开号:WO2015056213A1
    公开(公告)日:2015-04-23
    The invention provides compounds of the formula (I) wherein B is a nucleobase selected from the groups (a) to (d): and the other variables are as defined in the claims, which are of use in the treatment or prophylaxis of hepatitis C virus infection, and related aspects.
    这项发明提供了公式(I)中的化合物,其中B是从(a)到(d)组中选择的核碱基:其他变量如索权中所定义,这些化合物可用于治疗或预防丙型肝炎病毒感染及相关方面。
  • PYRAZOLE COMPOUND AND PHARMACEUTICAL USE THEREOF
    申请人:MIURA Tomoya
    公开号:US20130085132A1
    公开(公告)日:2013-04-04
    The present invention provides a pyrazole compound of the following general Formula [Ib] having SGLT1 inhibitory activity, or a pharmaceutically acceptable salt thereof, a pharmaceutical composition comprising the same, and its pharmaceutical use: wherein each symbol is the same as defined in the description.
    本发明提供了一种具有SGLT1抑制活性的下式[Ib]所示的吡唑化合物、或其药物可接受的盐、包含该化合物的药物组合物及其医药用途: 其中每个符号如说明书中所定义。
  • [EN] NOVEL ANTIVIRAL AND ANTITUMORAL COMPOUNDS<br/>[FR] NOUVEAUX COMPOSÉS ANTIVIRAUX ET ANTITUMORAUX
    申请人:UNIV LEUVEN KATH
    公开号:WO2015158913A1
    公开(公告)日:2015-10-22
    The present invention relates to novel phosphate-modified nucleosides, such as phosphoramidate nucleosides. The invention also relates to the use of these novel phosphate-modified nucleosides to treat or prevent viral infections and proliferative diseases (such as cancer) and their use to manufacture a medicine to treat or prevent viral infections and proliferative diseases particularly infections with viruses belonging to the HCV family.
    本发明涉及新型磷酸酯修饰核苷,如磷酰胺酸酯核苷。该发明还涉及利用这些新型磷酸酯修饰核苷来治疗或预防病毒感染和增殖性疾病(如癌症),以及它们用于制造用于治疗或预防病毒感染和增殖性疾病,特别是感染HCV家族病毒的药物。
  • [EN] PROCESS FOR THE PREPARATION OF AN (HETERO)ARYLAMINE<br/>[FR] PROCEDE DE PREPARATION D'UNE (HETERO)ARYLAMINE
    申请人:DSM IP ASSETS BV
    公开号:WO2006009431A1
    公开(公告)日:2006-01-26
    The present invention relates to a process for the preparation of an (hetero)arylamine, wherein an optionally substituted (hetero)aromatic bromide compound is contacted with a nucleophilic organic nitrogen-containing compound in the presence of a base, and a catalyst comprising a copper atom or ion and at least one ligand, said ligand comprising at least one coordinating oxygen atom, and if said oxygen atom is part of an OH group, then said OH group is attached to an aliphatic spa carbon atom or to a vinylic carbon atom.
    本发明涉及一种用于制备(杂)芳胺的方法,其中选择性取代的(杂)芳基溴化合物与含有亲核有机氮基团的化合物在碱的存在下接触,并且使用包含铜原子或离子和至少一种配体的催化剂,所述配体包含至少一个配位氧原子,如果所述氧原子是羟基的一部分,则所述羟基连接到一个脂肪烷基碳原子或乙烯基碳原子。
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