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2-叔丁基-1,3-噻唑 | 13623-12-6

中文名称
2-叔丁基-1,3-噻唑
中文别名
——
英文名称
2-(tert-butyl)thiazole
英文别名
2-tert-Butyl-1,3-thiazole
2-叔丁基-1,3-噻唑化学式
CAS
13623-12-6
化学式
C7H11NS
mdl
——
分子量
141.237
InChiKey
DQAIZGWCKXJRSP-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:
    174.1±9.0 °C(Predicted)
  • 密度:
    1.017±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.7
  • 重原子数:
    9
  • 可旋转键数:
    1
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.57
  • 拓扑面积:
    41.1
  • 氢给体数:
    0
  • 氢受体数:
    2

安全信息

  • 海关编码:
    2934100090

SDS

SDS:27d37783da70592ceb244a3f137b19c3
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反应信息

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文献信息

  • PYRIMIDINE-FUSED CYCLIC COMPOUND, PREPARATION METHOD THEREFOR AND APPLICATION THEREOF
    申请人:SHANGHAI BLUERAY BIOPHARMA CO., LTD.
    公开号:US20210053989A1
    公开(公告)日:2021-02-25
    Disclosed in the present disclosure are a pyrimidine-fused cyclic compound or a pharmaceutically acceptable salt, hydrate, prodrug, stereoisomer, solvate or isotope labeled compound thereof. Also provided in the present disclosure are a preparation method for the compound, a composition comprising the compound and a use of the compound for the preparation of a medicament for the prevention and/or treatment of a disease or condition associated with abnormal SHP2 activity.
    本公开涉及一种嘧啶融合的环状化合物或其药用可接受的盐、合物、前药、立体异构体、溶剂合物或同位素标记化合物。本公开还提供了该化合物的制备方法、包含该化合物的组合物以及该化合物用于制备与异常SHP2活性相关的疾病或病况的药物的用途。
  • SUBSTITUTED HETEROCYCLES AS ANTIVIRAL AGENTS
    申请人:Enanta Pharmaceuticals, Inc.
    公开号:US20190224188A1
    公开(公告)日:2019-07-25
    The present invention discloses compounds of Formula (I), and pharmaceutically acceptable salts thereof: which inhibit the protein(s) encoded by hepatitis B virus (HBV) or interfere with the function of the HBV life cycle of the hepatitis B virus and are also useful as antiviral agents. The present invention further relates to pharmaceutical compositions comprising the aforementioned compounds for administration to a subject suffering from HBV infection. The invention also relates to methods of treating an HBV infection in a subject by administering a pharmaceutical composition comprising the compounds of the present invention.
    本发明公开了式(I)的化合物及其药学上可接受的盐: 这些化合物抑制由乙型肝炎病毒(HBV)编码的蛋白质或干扰乙型肝炎病毒的生命周期功能,并且还可用作抗病毒剂。本发明还涉及包括上述化合物的药物组合物,用于治疗患有HBV感染的受试者。该发明还涉及通过给予包含本发明化合物的药物组合物来治疗受试者的HBV感染的方法。
  • Modulators of Cystic Fibrosis Transmembrane Conductance Regulator
    申请人:VERTEX PHARMACEUTICALS INCORPORATED
    公开号:US20160095858A1
    公开(公告)日:2016-04-07
    The present invention features a compound of formula I: or a pharmaceutically acceptable salt thereof, where R 1 , R 2 , R 3 , W, X, Y, Z, n, o, p, and q are defined herein, for the treatment of CFTR mediated diseases, such as cystic fibrosis. The present invention also features pharmaceutical compositions, method of treating, and kits thereof.
    本发明涉及一种具有以下化学式I的化合物: 或其药用可接受的盐,其中R 1 ,R 2 ,R 3 ,W,X,Y,Z,n,o,p和q在此处定义,用于治疗CFTR介导的疾病,如囊性纤维化。本发明还涉及药物组合物、治疗方法和相关工具包。
  • BICYCLIC HETEROARYL COMPOUNDS AND USES THEREOF
    申请人:Revolution Medicines, Inc.
    公开号:US20210139517A1
    公开(公告)日:2021-05-13
    The present disclosure is directed to modulators of SOS1 and their use in the treatment of disease. Also disclosed are pharmaceutical compositions comprising the same.
    本公开涉及SOS1的调节剂及其在治疗疾病中的应用。还公开了包含相同成分的药物组合物。
  • CYCLOALKYLIDENE AND HETEROCYCLOALKYLIDENE INHIBITOR COMPOUNDS
    申请人:Melvin, JR. Lawrence S.
    公开号:US20100022543A1
    公开(公告)日:2010-01-28
    The present invention provides a compound of general Formula (I) having histone deacetylase (HDAC) inhibitory activity, a pharmaceutical composition comprising the compound, and a method useful to treat diseases using the compound.
    本发明提供了一种具有组蛋白去乙酰化酶(HDAC)抑制活性的一般式(I)化合物,包括该化合物的药物组合物,以及使用该化合物治疗疾病的方法。
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