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1-甲基-1H-吲唑-5-羧醛 | 872607-89-1

中文名称
1-甲基-1H-吲唑-5-羧醛
中文别名
1-甲基-1H-吲唑-5-甲醛;1 -甲基- 1H-吲唑- 5 -甲醛
英文名称
1-methyl-1H-indazole-5-carbaldehyde
英文别名
1-methylindazole-5-carbaldehyde
1-甲基-1H-吲唑-5-羧醛化学式
CAS
872607-89-1
化学式
C9H8N2O
mdl
MFCD11109365
分子量
160.175
InChiKey
AKVDMQHGNSYFAG-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:
    311.8±15.0 °C(Predicted)
  • 密度:
    1.21±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    1
  • 重原子数:
    12
  • 可旋转键数:
    1
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.111
  • 拓扑面积:
    34.9
  • 氢给体数:
    0
  • 氢受体数:
    2

安全信息

  • 海关编码:
    2933990090
  • 危险性防范说明:
    P280,P305+P351+P338
  • 危险性描述:
    H302

SDS

SDS:42f5e4f289312185735cfbff1be59388
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Material Safety Data Sheet

Section 1. Identification of the substance
Product Name: 1-Methyl-1h-indazole-5-carbaldehyde
Synonyms:

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

Section 3. Composition/information on ingredients.
Ingredient name: 1-Methyl-1h-indazole-5-carbaldehyde
CAS number: 872607-89-1

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: C9H8N2O
Molecular weight: 160.2

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

反应信息

  • 作为反应物:
    描述:
    参考文献:
    名称:
    Potent and Selective Inhibitors of CDPK1 from T. gondii and C. parvum Based on a 5-Aminopyrazole-4-carboxamide Scaffold
    摘要:
    5-Aminopyrazole-4-carboxamide was used as an alternative scaffold to substitute for the pyrazolopyrimidine of a known "bumped kinase inhibitor" to create selective inhibitors of calcium-dependent protein kinase-1 from both Toxoplasma gondii and Cryptosporidium parvum. Compounds with low nanomolar inhibitory potencies against the target enzymes were obtained. The most selective inhibitors also exhibited submicromolar activities in T. gondii cell proliferation assays and were shown to be non-toxic to mammalian cells.
    DOI:
    10.1021/ml400315s
  • 作为产物:
    描述:
    5-溴-2-氟苯甲醛正丁基锂乙基溴化镁 、 sodium hydride 、 potassium carbonate一水合肼 作用下, 以 四氢呋喃N,N-二甲基甲酰胺甲苯 为溶剂, 反应 7.0h, 生成 1-甲基-1H-吲唑-5-羧醛
    参考文献:
    名称:
    [EN] HETEROCYCLIC OXIME COMPOUNDS
    [FR] COMPOSÉS D'OXIMES HÉTÉROCYCLIQUES
    摘要:
    该发明涉及公式(I)的化合物及其盐,其中取代基如规范中所定义;公式(I)的化合物用于治疗人体或动物体,特别是针对c-Met酪氨酸激酶介导的疾病或症状;公式(I)的化合物用于制造治疗此类疾病的药物;包含公式(I)的化合物的药物组合物,可选地与组合伙伴一起,并且用于制备公式(I)的化合物的方法。
    公开号:
    WO2011020861A1
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文献信息

  • Synthesis and identification of heteroaromatic<i>N</i>-benzyl sulfonamides as potential anticancer agents
    作者:Megan D. Hopkins、Felagot A. Abebe、Kristina A. Scott、Garett L. Ozmer、Alec A. Sheir、Lucas J. Schroeder、Robert J. Sheaff、Angus A. Lamar
    DOI:10.1039/c9ob01694e
    日期:——
    assay. The cell viability investigation identifies a subset of N-benzylic sulfonamides derived from the indole scaffold to be targeted for further development into novel molecules with potential therapeutic value. The most cytotoxic of the compounds prepared, AAL-030, exhibited higher potency than other well-known anticancer agents Indisulam and ABT-751.
    磺酰胺类是在许多药物中普遍存在的关键性生物等排体,但是,直接由杂芳基醛试剂生产的可用方法仍然令人惊讶地受到限制。已经开发了一种新的方法,用于将磺酰胺单元区域选择性地掺入杂芳烃支架中,并在其中报道。结果,通过原位还原中间体N,通过两步(一锅)形成,制备了多种伯苄基N-烷基磺酰胺。-磺酰亚胺在温和的实际条件下。使用细胞滴度蓝测定法已经针对多种细胞系针对细胞毒性作用筛选了该化合物。细胞活力研究确定了衍生自吲哚支架的N-苄基磺酰胺的子集,可将其进一步开发成具有潜在治疗价值的新型分子。所制备化合物中最具细胞毒性的化合物AAL-030比其他知名的抗癌药Indisulam和ABT-751表现出更高的效力。
  • QUINAZOLINONES AS PARP14 INHIBITORS
    申请人:Ribon Therapeutics Inc.
    公开号:US20190194174A1
    公开(公告)日:2019-06-27
    The present invention relates to quinazolinones and related compounds which are inhibitors of PARP14 and are useful, for example, in the treatment of cancer and inflammatory diseases.
    本发明涉及喹唑啉酮和相关化合物,它们是PARP14的抑制剂,例如在癌症和炎症性疾病的治疗中是有用的。
  • [EN] COMPOUNDS AND COMPOSITIONS FOR THE TREATMENT OF TUMORS<br/>[FR] COMPOSÉS ET COMPOSITIONS POUR LE TRAITEMENT DE TUMEURS
    申请人:FONDAZIONE ST ITALIANO TECNOLOGIA
    公开号:WO2021116999A1
    公开(公告)日:2021-06-17
    The present invention relates to compounds of Formula (Ia) or pharmaceutically acceptable salts, hydrates, solvates, clathrates, polymorphs, stereoisomers thereof. It further discloses a pharmaceutical composition comprising compounds of Formula (Ia) and the use of compounds of Formula (Ib), in particular for the use in the treatment of diseases or disorders wherein disrupting Rad51-BRCA2 interaction is beneficial.
    本发明涉及式(Ia)的化合物或药学上可接受的盐、合物、溶剂合物、包合物、多晶型、立体异构体,还揭示了包含式(Ia)的化合物的药物组合物以及利用式(Ib)的化合物,特别是用于治疗破坏Rad51-BRCA2相互作用有益的疾病或紊乱的用途。
  • [EN] IMIDAZO [1,2-B] PYRIDAZINE DERIVATIVES FOR THE TREATMENT OF C-MET TYROSINE KINASE MEDIATED DISEASE<br/>[FR] DÉRIVÉS D'IMIDAZO[1,2-B]PYRIDAZINE POUR LE TRAITEMENT DE MALADIES MÉDIÉES PAR LA TYROSINE KINASE C-MET
    申请人:NOVARTIS AG
    公开号:WO2009106577A1
    公开(公告)日:2009-09-03
    The invention relates to compounds of formula (I) and salts thereof, formula (I) wherein the substituents are as defined in the specification, the application of a compound of formula (I) in a process for the treatment of the human or animal body, in particular with regard to C-Met tyrosine kinase mediated disease; the use of a compound of formula (I) for manufacturing a medicament for the treatment of such diseases; pharamaceutical compositions comprising a compound of the formula (I), optionally in the presence of a combination partner; processes for the preparation of a compound of formula (I).
    该发明涉及式(I)化合物及其盐,式(I)中取代基如规范中所定义,式(I)化合物在用于治疗人体或动物体内的过程中的应用,特别是涉及C-Met酪氨酸激酶介导的疾病;式(I)化合物用于制造治疗此类疾病的药物;包含式(I)化合物的药物组合物,可选地与组合伙伴一起;式(I)化合物的制备方法。
  • [EN] HETEROCYCLIC HYDRAZONE COMPOUNDS AND THEIR USES TO TREAT CANCER AND INFLAMMATION<br/>[FR] COMPOSÉS HYDRAZONE HÉTÉROCYCLIQUES ET LEURS UTILISATIONS POUR TRAITER LE CANCER ET L'INFLAMMATION
    申请人:NOVARTIS AG
    公开号:WO2011018454A1
    公开(公告)日:2011-02-17
    The invention relates to compounds of formula (I) and salts thereof: wherein the substituents are as defined in the specification; a compound of formula (I) for use in the treatment of the human or animal body, in particular with regard to c-Met tyrosine kinase mediated diseases or conditions; the use of a compound of formula (I) for manufacturing a medicament for the treatment of such diseases; pharmaceutical compositions comprising a compound of the formula (I), optionally in the presence of a combination partner, and processes for the preparation of a compound of formula (I).
    该发明涉及公式(I)的化合物及其盐:其中取代基如规范中所定义;公式(I)的化合物用于治疗人体或动物体,特别是针对c-Met酪氨酸激酶介导的疾病或症状;公式(I)的化合物用于制造治疗此类疾病的药物;包含公式(I)的化合物的药物组合物,可选地与组合伙伴一起,并且公式(I)的化合物的制备方法。
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