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2-氟-6-甲基苯基硼酸 | 887471-69-4

中文名称
2-氟-6-甲基苯基硼酸
中文别名
——
英文名称
(2-fluoro-6-methylphenyl)boronic acid
英文别名
——
2-氟-6-甲基苯基硼酸化学式
CAS
887471-69-4
化学式
C7H8BFO2
mdl
——
分子量
153.949
InChiKey
UGGFAYXDRNOISZ-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:
    285.9±50.0 °C(Predicted)
  • 密度:
    1.20±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    -0.19
  • 重原子数:
    11
  • 可旋转键数:
    1
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.14
  • 拓扑面积:
    40.5
  • 氢给体数:
    2
  • 氢受体数:
    3

安全信息

  • 危险性防范说明:
    P261,P280,P305+P351+P338
  • 危险性描述:
    H302,H312,H315,H319,H332,H335
  • 储存条件:
    存储条件:2-8℃,干燥且密封。

SDS

SDS:bd906e8bd070416198a53ae40b20a7bb
查看
Material Safety Data Sheet

Section 1. Identification of the substance
Product Name: 2-Fluoro-6-methylphenylboronic acid
Synonyms:

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

Section 3. Composition/information on ingredients.
Ingredient name: 2-Fluoro-6-methylphenylboronic acid
CAS number: 887471-69-4

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, refrigerated.
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: C7H8BFO2
Molecular weight: 153.9

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

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

反应信息

  • 作为反应物:
    描述:
    2-氟-6-甲基苯基硼酸 生成 (7-(2-Fluoro-6-methylphenyl)-2-azaspiro[3.5]nonan-2-yl)((1s,3s)-3-hydroxy-3-methylcyclobutyl)methanone
    参考文献:
    名称:
    CYCLOBUTYL AMIDE MONOACYLGLYCEROL LIPASE MODULATORS
    摘要:
    式(I)的化合物及其药用盐、同位素、N-氧化物、溶剂合物和立体异构体,包含它们的药物组合物,制备它们的方法以及使用它们的方法,包括用于治疗与MGL调节相关的疾病状态、疾病和症状的方法,如与疼痛、精神障碍、神经障碍(包括但不限于抑郁症、重度抑郁症、治疗抵抗性抑郁症、焦虑性抑郁症、自闭症谱系障碍、阿斯伯格综合征和躁狂症)、癌症和眼部疾病相关的疾病状态、疾病和症状:其中R1、R3和L如本文所定义。
    公开号:
    US20220089538A1
  • 作为产物:
    描述:
    2-溴-3-氟甲苯硼酸三异丙酯叔丁基锂盐酸 作用下, 以 乙醚正戊烷 为溶剂, 反应 1.0h, 以43%的产率得到2-氟-6-甲基苯基硼酸
    参考文献:
    名称:
    New bicyclic compounds as crac channel modulators
    摘要:
    这项发明涉及一种新型化合物,它们是CRAC通道活性的抑制剂。该发明还涉及含有这些化合物的药物组合物,它们的制备方法以及它们在治疗中的应用。
    公开号:
    EP2738172A1
点击查看最新优质反应信息

文献信息

  • CYCLIC ETHER PYRAZOL-4-YL-HETEROCYCLYL-CARBOXAMIDE COMPOUNDS AND METHODS OF USE
    申请人:Genentech, Inc.
    公开号:US20140088117A1
    公开(公告)日:2014-03-27
    Cyclic ether pyrazol-4-yl-heterocyclyl-carboxamide compounds of Formula I, including stereoisomers, geometric isomers, tautomers, and pharmaceutically acceptable salts thereof, wherein R 2 is a cyclic ether and X is thiazolyl, pyrazinyl, pyridinyl, or pyrimidinyl, are useful for inhibiting Pim kinase, and for treating disorders such as cancer mediated by Pim kinase. Methods of using compounds of Formula I for in vitro, in situ, and in vivo diagnosis, prevention or treatment of such disorders in mammalian cells, or associated pathological conditions, are disclosed.
    公式I的环醚吡唑-4-基-杂环基-羧酰胺化合物,包括立体异构体、几何异构体、互变异构体和其药学上可接受的盐,其中R2为环醚,X为噻唑基、吡啶基、吡啶基或嘧啶基,可用于抑制Pim激酶,并用于治疗由Pim激酶介导的癌症等疾病。公开了使用公式I化合物进行体外、体内和体内诊断、预防或治疗哺乳动物细胞中的这类疾病或相关病理条件的方法。
  • [EN] INHIBITORS OF THE WNT SIGNALLING PATHWAYS<br/>[FR] INHIBITEURS DES VOIES DE SIGNALISATION WNT
    申请人:BAYER PHARMA AG
    公开号:WO2015140196A1
    公开(公告)日:2015-09-24
    The present invention relates to inhibitors of the Wnt signalling pathways of general formula (I) as described and defined herein, to methods of preparing said compounds, to intermediate compounds useful for preparing said compounds, to pharmaceutical compositions and combinations comprising said compounds and to the use of said compounds for manufacturing a pharmaceutical composition for the treatment or prophylaxis of a disease, in particular of a hyper- proliferative disorder, as a sole agent or in combination with other active ingredients.
    本发明涉及通式(I)所述和定义的Wnt信号通路抑制剂,涉及制备该类化合物的方法,有用于制备该类化合物的中间化合物,包含该类化合物的药物组合物和组合物,以及利用该类化合物制造用于治疗或预防疾病的药物组合物,特别是用作唯一药剂或与其他活性成分组合使用时,用于治疗或预防过度增殖性疾病。
  • NAPHTHYRIDINES AS INHIBITORS OF HPK1
    申请人:Genentech, Inc.
    公开号:US20180282328A1
    公开(公告)日:2018-10-04
    Naphthyridine compounds and their use as inhibitors of HPK1 are described. The compounds are useful in treating HPK1-dependent disorders and enhancing an immune response. Also described are methods of inhibiting HPK1, methods of treating HPK1-dependent disorders, methods for enhancing an immune response, and methods for preparing the naphthyridine compounds.
    萘啶化合物及其作为HPK1抑制剂的用途被描述。这些化合物在治疗HPK1依赖性疾病和增强免疫反应方面很有用。还描述了抑制HPK1的方法、治疗HPK1依赖性疾病的方法、增强免疫反应的方法以及制备萘啶化合物的方法。
  • PYRAZOLOPYRIDINE COMPOUNDS AND USES THEREOF
    申请人:Incyte Corporation
    公开号:US20180072720A1
    公开(公告)日:2018-03-15
    Disclosed are compounds of Formula (I), methods of using the compounds for inhibiting HPK1 activity and pharmaceutical compositions comprising such compounds. The compounds are useful in treating, preventing or ameliorating diseases or disorders associated with HPK1 activity such as cancer.
    揭示了化合物的公式(I),使用这些化合物抑制HPK1活性的方法以及包含这些化合物的药物组合物。这些化合物在治疗、预防或改善与HPK1活性相关的疾病或紊乱方面是有用的,如癌症。
  • 吡啶并嘧啶酮类化合物及其应用
    申请人:广州必贝特医药技术有限公司
    公开号:CN112159405A
    公开(公告)日:2021-01-01
    本发明提供了具有通式(II)所示结构的吡啶并嘧啶酮类化合物及其应用。研究证明,本发明提供的化合物可以有效抑制KRAS G12C突变。KRAS突变在肿瘤中占比很大,且目前没有获得批准药物对其进行治疗,本发明提供的化合物有潜力成为携带KRAS G12C突变的恶性肿瘤(尤其是非小细胞肺癌(NSCLC)和直结肠癌)的治疗药物,有较大的应用价值。
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