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6-羟基-2-甲基-2H-吲唑 | 52470-67-4

中文名称
6-羟基-2-甲基-2H-吲唑
中文别名
——
英文名称
2-methyl-6-hydroxyindazole
英文别名
6-hydroxy-2-methylindazole;2-methyl-2H-indazol-6-ol;6-Hydroxy-2-methylindazol;2-methylindazol-6-ol
6-羟基-2-甲基-2H-吲唑化学式
CAS
52470-67-4
化学式
C8H8N2O
mdl
MFCD00456127
分子量
148.164
InChiKey
VREJRTXKMYMPEV-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:
    344.0±15.0 °C(Predicted)
  • 密度:
    1.27±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    1.6
  • 重原子数:
    11
  • 可旋转键数:
    0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.125
  • 拓扑面积:
    38
  • 氢给体数:
    1
  • 氢受体数:
    2

安全信息

  • 海关编码:
    2933990090
  • 危险性防范说明:
    P261,P264,P270,P271,P280,P301+P312+P330,P302+P352+P312,P304+P340+P312,P305+P351+P338,P332+P313,P337+P313,P362,P363,P403+P233,P405,P501
  • 危险性描述:
    H302+H312+H332,H315,H319,H335

反应信息

  • 作为反应物:
    描述:
    6-羟基-2-甲基-2H-吲唑盐酸 、 sodium nitrite 作用下, 以 为溶剂, 以85%的产率得到2-methyl-6-hydroxy-7-nitrosoindazole
    参考文献:
    名称:
    Synthesis of 5-hydroxy-4-nitrosobenzotriazoles and 6-hydroxy-7-nitrosoindazoles and their splitting into ?-triazolyl- and ?-pyrazolylacrylic acids
    摘要:
    DOI:
    10.1007/bf00478859
  • 作为产物:
    描述:
    alkaline earth salt of/the/ methylsulfuric acid 在 硫酸 作用下, 生成 6-羟基-2-甲基-2H-吲唑
    参考文献:
    名称:
    v. Auwers; Demuth, Justus Liebigs Annalen der Chemie, 1927, vol. 451, p. 285,302
    摘要:
    DOI:
点击查看最新优质反应信息

文献信息

  • [EN] 2-(INDAZOL-5-YL)-6-(PIPERIDIN-4-YL)-1,7-NAPHTHYRIDINE DERIVATIVES AND RELATED COMPOUNDS AS MODULATORS FOR SPLICING NUCLEIC ACIDS AND FOR THE TREATMENT OF PROLIFERATIVE DISEASES<br/>[FR] DÉRIVÉS DE 2-(INDAZOL-5-YL)-6-(PIPERIDIN-4-YL)-1,7-NAPHTHYRIDINE ET COMPOSÉS Y RELATIFS EN TANT QUE MODULATEURS POUR L'ÉPISSAGE D'ACIDES NUCLÉIQUES ET POUR LE TRAITEMENT DE MALADIES PROLIFÉRANTES
    申请人:REMIX THERAPEUTICS INC
    公开号:WO2022006550A1
    公开(公告)日:2022-01-06
    The present disclosure features compounds of formula (l-a) and of formula (II) and pharmaceutical compositions thereof. The present disclosure further discloses the compounds of formula (I- a) and (II) and their compositions for use in methods of modulating nucleic acid splicing, e.g., splicing of a pre-mRNA, as well as said compounds for use in methods of treating e.g.: • proliferative diseases, such as e.g. cancer, benign neoplasms or angiogenesis, • neurological diseases or disorders, such as e.g. Huntington's disease, • autoimmune diseases or disorders, immunodeficiency diseases or disorders, lysosomal storage disease or disorder, cardiovascular diseases or disorders, metabolic diseases or disorders, respiratory diseases or disorders, renal diseases or disorders, or infectious diseases. Exemplary compounds are e.g. 2-(indazol-5-yl)-6-(piperidin-4-yl)-l,7- naphthyridine derivatives and similar compounds.
    本公开涉及公式(l-a)和公式(II)的化合物及其药物组合物。本公开还揭示了公式(I-a)和(II)的化合物及其组合物,用于调节核酸剪接的方法,例如,剪接预mRNA,以及用于治疗方法的化合物,例如: •增殖性疾病,如癌症、良性肿瘤或血管生成等, •神经系统疾病或障碍,如亨廷顿病等, •自身免疫性疾病或障碍、免疫缺陷性疾病或障碍、溶酶体贮积病或障碍、心血管疾病或障碍、代谢性疾病或障碍、呼吸系统疾病或障碍、肾脏疾病或障碍或传染性疾病。示例化合物包括2-(吲哚-5-基)-6-(哌啶-4-基)-1,7-萘啶生物和类似化合物。
  • [EN] ANTIVIRAL AGENTS AND USES THEREOF<br/>[FR] AGENTS ANTIVIRAUX ET LEURS UTILISATIONS
    申请人:UNIV GRIFFITH
    公开号:WO2021016670A1
    公开(公告)日:2021-02-04
    The present invention relates to a compound of formula (I), or a pharmaceutically acceptable salt thereof: Formula (I) In which R3 is selected from the group consisting of optionally substituted N-linked naphthotriazole, optionally substituted N-linked indazole, and certain N-linked triazoles. The present invention also relates to uses of the compounds in treating a disease, disorder or condition caused by viral infection, and pharmaceutical compositions comprising the compounds.
    本发明涉及一种化合物,其化学式为(I),或其药学上可接受的盐:化学式(I) 其中R3选自可选择的取代N-连接的三唑、可选择的取代N-连接的吲唑和某些N-连接的三唑组成的群。本发明还涉及将该化合物用于治疗由病毒感染引起的疾病、疾病或病况的用途,以及包含该化合物的药物组合物。
  • [EN] HER2 MUTATION INHIBITORS<br/>[FR] INHIBITEURS DE MUTATION HER2
    申请人:ARRAY BIOPHARMA INC
    公开号:WO2022269531A1
    公开(公告)日:2022-12-29
    This invention relates to compounds of Formula (I): (I), and enantiomers thereof, and to pharmaceutically acceptable salts of Formula (I) and said enantiomers, wherein A, L2, R1, R2, R3, R4, and n are as defined herein. The invention further relates to pharmaceutical compositions comprising such compounds and salts, and to methods and uses of such compounds, salts, and compositions for the treatment of abnormal cell growth, including cancer, in a subject in need thereof.
    本发明涉及公式(I)化合物:(I)及其对映体,以及公式(I)及其对映体的药学上可接受的盐,其中A,L2,R1,R2,R3,R4和n如本文所定义。本发明还涉及包含此类化合物和盐的制药组合物,以及使用此类化合物、盐和组合物治疗需要的主体中的异常细胞生长,包括癌症的方法和用途。
  • Sequeria, S.; Seshadri, S., Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry, 1987, vol. 26, # 1-12, p. 436 - 439
    作者:Sequeria, S.、Seshadri, S.
    DOI:——
    日期:——
  • SEQUERIA, S.;SESHADRI, S., INDIAN J. CHEM., 26,(1987) N 5, 436-439
    作者:SEQUERIA, S.、SESHADRI, S.
    DOI:——
    日期:——
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