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1H-吲唑-5-甲酸乙酯 | 192944-51-7

中文名称
1H-吲唑-5-甲酸乙酯
中文别名
1H-吲唑-5-羧酸乙酯;5-吲唑羧酸乙酯
英文名称
1H-indazole-5-carboxylic acid ethyl ester
英文别名
ethyl 1H-indazole-5-carboxylate;ethyl indazole-5-carboxylate;5-Ethoxycarbonylindazole
1H-吲唑-5-甲酸乙酯化学式
CAS
192944-51-7
化学式
C10H10N2O2
mdl
——
分子量
190.202
InChiKey
SKABXDPLIJIWLR-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

  • 熔点:
    122-124℃
  • 沸点:
    353.9±15.0 °C(Predicted)
  • 密度:
    1.272±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.4
  • 重原子数:
    14
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.2
  • 拓扑面积:
    55
  • 氢给体数:
    1
  • 氢受体数:
    3

安全信息

  • 安全说明:
    S26,S36/37/39
  • 危险类别码:
    R36/37/38
  • 危险性防范说明:
    P261,P305+P351+P338
  • 危险性描述:
    H302,H315,H319,H335

SDS

SDS:5b0e7b7b6eaf425f4f52b1c0733438bf
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Material Safety Data Sheet

Section 1. Identification of the substance
Product Name: Ethyl 1h-indazole-5-carboxylate
Synonyms:

Section 2. Hazards identification
Harmful by inhalation, in contact with skin, and if swallowed.

Section 3. Composition/information on ingredients.
Ingredient name: Ethyl 1h-indazole-5-carboxylate
CAS number: 192944-51-7

Section 4. First aid measures
Skin contact: Immediately wash skin with copious amounts of water for at least 15 minutes while removing
contaminated clothing and shoes. If irritation persists, seek medical attention.
Eye contact: Immediately wash skin with copious amounts of water for at least 15 minutes. Assure adequate
flushing of the eyes by separating the eyelids with fingers. If irritation persists, seek medical
attention.
Inhalation: Remove to fresh air. In severe cases or if symptoms persist, seek medical attention.
Ingestion: Wash out mouth with copious amounts of water for at least 15 minutes. Seek medical attention.

Section 5. Fire fighting measures
In the event of a fire involving this material, alone or in combination with other materials, use dry
powder or carbon dioxide extinguishers. Protective clothing and self-contained breathing apparatus
should be worn.

Section 6. Accidental release measures
Personal precautions: Wear suitable personal protective equipment which performs satisfactorily and meets local/state/national
standards.
Respiratory precaution: Wear approved mask/respirator
Hand precaution: Wear suitable gloves/gauntlets
Skin protection: Wear suitable protective clothing
Eye protection: Wear suitable eye protection
Methods for cleaning up: Mix with sand or similar inert absorbent material, sweep up and keep in a tightly closed container
for disposal. See section 12.
Environmental precautions: Do not allow material to enter drains or water courses.

Section 7. Handling and storage
Handling: This product should be handled only by, or under the close supervision of, those properly qualified
in the handling and use of potentially hazardous chemicals, who should take into account the fire,
health and chemical hazard data given on this sheet.
Store in closed vessels.
Storage:

Section 8. Exposure Controls / Personal protection
Engineering Controls: Use only in a chemical fume hood.
Personal protective equipment: Wear laboratory clothing, chemical-resistant gloves and safety goggles.
General hydiene measures: Wash thoroughly after handling. Wash contaminated clothing before reuse.

Section 9. Physical and chemical properties
Appearance: Not specified
Boiling point: No data
No data
Melting point:
Flash point: No data
Density: No data
Molecular formula: C10H10N2O2
Molecular weight: 190.2

Section 10. Stability and reactivity
Conditions to avoid: Heat, flames and sparks.
Materials to avoid: Oxidizing agents.
Possible hazardous combustion products: Carbon monoxide, nitrogen oxides.

Section 11. Toxicological information
No data.

Section 12. Ecological information
No data.

Section 13. Disposal consideration
Arrange disposal as special waste, by licensed disposal company, in consultation with local waste
disposal authority, in accordance with national and regional regulations.

Section 14. Transportation information
Non-harzardous for air and ground transportation.

Section 15. Regulatory information
No chemicals in this material are subject to the reporting requirements of SARA Title III, Section
302, or have known CAS numbers that exceed the threshold reporting levels established by SARA
Title III, Section 313.


SECTION 16 - ADDITIONAL INFORMATION
N/A

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量
    • 1
    • 2

反应信息

  • 作为反应物:
    描述:
    1H-吲唑-5-甲酸乙酯1,1'-双(二苯基膦)二茂铁1,1'-双(二苯膦基)二茂铁二氯化钯(II)二氯甲烷复合物三乙胺 、 potassium hydroxide 作用下, 以 N,N-二甲基甲酰胺甲苯 为溶剂, 20.0~70.0 ℃ 、100.0 kPa 条件下, 反应 2.5h, 生成 5-ethyl 3-methyl 1H-Indazole-3,5-dicarboxylate
    参考文献:
    名称:
    通过钯催化3-碘吲唑羰基化反应合成3-吲唑羧酸酯和酰胺
    摘要:
    开发了一种简单有效的制备1 H-吲哚-3-羧酸酯和酰胺的方法。在甲醇或胺的存在下,对一系列官能化的3-碘吲唑进行Pd催化的羰基化反应,以中等至良好的收率得到标题化合物。对于大多数实例,反应在温和条件下干净地进行,该条件易于被允许进一步合成转化的多种官能团所耐受。 羰基化-酯-酰胺-烷氧基羰基化-氨基羰基化-碘吲唑-钯催化
    DOI:
    10.1055/s-0030-1260199
  • 作为产物:
    描述:
    4-氨基-3-甲基苯甲酸乙酯盐酸potassium acetate 作用下, 以 乙醇氯仿 为溶剂, 反应 37.0h, 生成 1H-吲唑-5-甲酸乙酯
    参考文献:
    名称:
    HETEROCYCLIC COMPOUND AND p27Kip1 DEGRADATION INHIBITOR
    摘要:
    提供了一种新型杂环化合物或其盐,用于选择性地抑制p27Kip1的降解。该化合物或其盐由以下式(1)表示:其中A代表烷基、环烷基、芳基或杂环基,基团A可能有取代基;环B代表5至8成员的单环杂环环或包含该单环杂环环的缩合环,环B可能有取代基;环C代表芳香环,环C可能有取代基;L代表包含3至5个原子的主链的连接物,所述原子选自碳原子、氮原子、氧原子和硫原子组成的群,其中主链中的至少一个原子是选自氮原子、氧原子和硫原子组成的杂原子,连接物L可能有取代基;n为0或1。
    公开号:
    US20130079306A1
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文献信息

  • [EN] SMALL MOLECULE ACTIVATORS OF NICOTINAMIDE PHOSPHORIBOSYLTRANSFERASE (NAMPT) AND USES THEREOF<br/>[FR] ACTIVATEURS À PETITES MOLÉCULES DE NICOTINAMIDE PHOSPHORIBOSYLTRANSFÉRASE (NAMPT) ET LEURS UTILISATIONS
    申请人:SANFORD BURNHAM PREBYS MEDICAL DISCOVERY INST
    公开号:WO2018132372A1
    公开(公告)日:2018-07-19
    Provided herein are small molecule activators of Nicotinamide Phosphoribosyltransferase (NAMPT), compositions comprising the compounds, and methods of using the compounds and compositions.
    本文提供了尼古丁酰胺磷酸核糖转移酶(NAMPT)的小分子激活剂,包括这些化合物的组合物,以及使用这些化合物和组合物的方法。
  • [EN] PGD2 RECEPTOR ANTAGONISTS FOR THE TREATMENT OF INFLAMMATORY DISEASES<br/>[FR] ANTAGONISTES DE RECEPTEUR DE LA PROSTAGLANDINE D2 POUR LE TRAITEMENT DE MALADIES INFLAMMATOIRES
    申请人:MILLENNIUM PHARM INC
    公开号:WO2005100321A1
    公开(公告)日:2005-10-27
    Disclosed herein are compounds represented by Structural Formula: (I) and (I-A). Also disclosed is the use of such compounds for inhibiting the G-protein coupled receptor referred to as chemoattractant receptor-homologous molecule expressed on Th2, or simply 'CRTH2' for the treatment of inflammatory disorders. The variables in Structural Formula (I) and (I-A) are defined herein.
    本文披露了由结构式(I)和(I-A)表示的化合物。还披露了利用这些化合物抑制称为趋化剂受体同源分子表达在Th2上的G蛋白偶联受体,简称为'CRTH2',用于治疗炎症性疾病。结构式(I)和(I-A)中的变量在此处被定义。
  • [EN] N-(1H-IMIDAZOL-2-YL)BENZAMIDE COMPOUND AND PHARMACEUTICAL COMPOSITION COMPRISING THE SAME AS ACTIVE INGREDIENT<br/>[FR] COMPOSÉ DE N-(1H-IMIDAZOL-2-YL)BENZAMIDE ET COMPOSITION PHARMACEUTIQUE LE COMPRENANT EN TANT QUE PRINCIPE ACTIF
    申请人:KAINOS MEDICINE INC
    公开号:WO2021066559A1
    公开(公告)日:2021-04-08
    N-(1H-imidazol-2-yl)benzamide compound of formula (I), or a pharmaceutically acceptable salt, a prodrug, a solvate, or a stereoisomer thereof which is a novel compound exhibiting excellent inhibitory activity against IRAK-4, can be used without side effects for efficient prevention and treatment of diseases mediated by IRAK-4 receptors, particularly autoimmune diseases or lymphomas.
    N-(1H-咪唑-2-基)苯甲酰胺化合物的化学式(I),或其药学上可接受的盐、前药、溶剂合物或立体异构体,是一种新型化合物,表现出对IRAK-4的优异抑制活性,可用于高效预防和治疗由IRAK-4受体介导的疾病,特别是自身免疫疾病或淋巴瘤,且无副作用。
  • [EN] AMIDE COMPOUNDS FOR TREATMENT OF IMMUNE AND INFLAMMATORY DISORDERS<br/>[FR] COMPOSÉS AMIDE POUR LE TRAITEMENT DE TROUBLES IMMUNITAIRES ET INFLAMMATOIRES
    申请人:ACHILLION PHARMACEUTICALS INC
    公开号:WO2017035401A1
    公开(公告)日:2017-03-02
    Compounds, methods of use, and processes for making inhibitors of complement Factor D are provided comprising Formula I, I" and I"' or a pharmaceutically acceptable salt or composition thereof. The inhibitors described herein target Factor D and inhibit or regulate the complement cascade. The inhibitors of Factor D described herein reduces the excessive activation of complement.
    提供包含公式I、I"和I"'或其药用可接受盐或组合物的补体因子D抑制剂的化合物、使用方法和制备过程。本文所述的抑制剂针对因子D并抑制或调节补体级联反应。本文所述的因子D抑制剂减少了补体的过度激活。
  • DI-AZETIDINYL DIAMIDE AS MONOACYLGLYCEROL LIPASE INHIBITORS
    申请人:Connolly Peter J.
    公开号:US20120058986A1
    公开(公告)日:2012-03-08
    Disclosed are compounds, compositions and methods for treating various diseases, syndromes, conditions and disorders, including pain. Such compounds are represented by Formula (I) as follows: wherein Q and Z are defined herein.
    揭示了用于治疗各种疾病、综合症、症状和障碍的化合物、组合物和方法,包括疼痛。这些化合物由以下式(I)表示: 其中Q和Z在此处定义。
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