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3-羟基-4-甲基苯硼酸 | 216019-35-1

中文名称
3-羟基-4-甲基苯硼酸
中文别名
(3-羟基-4-甲基)苯硼酸
英文名称
(3-hydroxy-4-methylphenyl)boronic acid
英文别名
3-hydroxy-4-methylbenzeneboronic acid;3-Hydroxy-4-methylphenylboronic acid
3-羟基-4-甲基苯硼酸化学式
CAS
216019-35-1
化学式
C7H9BO3
mdl
MFCD01074652
分子量
151.958
InChiKey
BVFGFBGCIAWVMF-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:
    357.3±52.0 °C(Predicted)
  • 密度:
    1.26±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    1.82
  • 重原子数:
    11
  • 可旋转键数:
    1
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.142
  • 拓扑面积:
    60.7
  • 氢给体数:
    3
  • 氢受体数:
    3

安全信息

  • 危险性防范说明:
    P261,P264,P270,P271,P280,P301+P312,P302+P352,P304+P340,P330,P363,P501
  • 危险性描述:
    H302,H312,H332

SDS

SDS:e793229143613c988055f5e01213dad4
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Material Safety Data Sheet

Section 1. Identification of the substance
Product Name: 3-Hydroxy-4-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: 3-Hydroxy-4-methylphenylboronic acid
CAS number: 216019-35-1

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, under −20◦C.
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: C7H9BO3
Molecular weight: 152.0

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

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:
    3-羟基-4-甲基苯硼酸四(三苯基膦)钯 、 lithium hydroxide monohydrate 、 sodium carbonate 作用下, 以 四氢呋喃甲醇甲苯 为溶剂, 生成 5-(3-hydroxy-4-methylphenyl)hex-5-enoic acid
    参考文献:
    名称:
    芳基官能化烯酸的对映选择性溴化
    摘要:
    使芳基取代的1,1-二取代的链烯基羧酸经受对映选择性的有机催化方案,以区域选择性的方式产生相应的δ-溴内酯。以高至高收率分离产物,对映体过量为18-88%。
    DOI:
    10.1016/j.tetlet.2020.151756
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文献信息

  • [EN] DIHYDROOXADIAZINONES<br/>[FR] DIHYDROOXADIAZINONES
    申请人:BAYER AG
    公开号:WO2019025562A1
    公开(公告)日:2019-02-07
    The present invention provides dihydrooxydiazinone compounds of general formula (I) : in which R1, R2, R3, and R4, are as defined herein, methods of preparing said compounds, intermediate compounds useful for preparing said compounds, pharmaceutical compositions and combinations comprising said compounds and the use of said compounds for manufacturing pharmaceutical compositions for the treatment or prophylaxis of diseases, in particular of hyperproliferative diseases, as a sole agent or in combination with other active ingredients.
    本发明提供了一般式(I)的二氢氧二氮酮化合物:其中R1、R2、R3和R4如本文所定义,制备所述化合物的方法,用于制备所述化合物的中间体化合物,包含所述化合物的药物组合物和组合物,以及利用所述化合物制造用于治疗或预防疾病的药物组合物,特别是治疗或预防过度增殖性疾病,作为唯一药剂或与其他活性成分组合使用。
  • [EN] HETEROCYCLIC COMPOUNDS AND METHODS OF USE<br/>[FR] COMPOSÉS HÉTÉROCYCLIQUES ET PROCÉDÉS D'UTILISATION
    申请人:MEDIVATION TECHNOLOGIES INC
    公开号:WO2015058084A1
    公开(公告)日:2015-04-23
    The present application discloses compounds that are inhibitors of Btk, compounds that are inhibitors of ΡΒΚδ, and compounds that are dual inhibitors of both Btk and PI3Kδ. Also described are methods for synthesizing such inhibitors and methods for using such inhibitors for the treatment of diseases wherein inhibition of Btk and PI3Kδ provides a therapeutic benefit to a patient having the disease.
    本申请公开了抑制Btk的化合物、抑制ΡΒΚδ的化合物,以及既是Btk又是PI3Kδ的双重抑制剂的化合物。还描述了合成这些抑制剂的方法,以及利用这些抑制剂治疗疾病的方法,其中抑制Btk和PI3Kδ对患有该疾病的患者提供治疗益处。
  • [EN] PYRAZOLOPYRIMIDINE MACROCYCLES AS INHIBITORS OF HUMAN IMMUNODEFICIENCY VIRUS REPLICATION<br/>[FR] MACROCYCLES DE PYRAZOLOPYRIMIDINE UTILISÉS EN TANT QU'INHIBITEURS DE LA RÉPLICATION DU VIRUS DE L'IMMUNODÉFICIENCE HUMAINE
    申请人:BRISTOL MYERS SQUIBB CO
    公开号:WO2015126743A1
    公开(公告)日:2015-08-27
    The disclosure generally relates to compounds of formula I, including compositions and methods for treating human immunodeficiency virus (HIV) infection. The disclosure provides novel inhibitors of HIV integrase, pharmaceutical compositions containing such compounds, and methods for using these compounds in the treatment of HIV infection.
    本公开通常涉及公式I的化合物,包括用于治疗人类免疫缺陷病毒(HIV)感染的组合物和方法。本公开提供了新的HIV整合酶抑制剂,包含此类化合物的药物组合物,以及使用这些化合物治疗HIV感染的方法。
  • [EN] FATTY ACID SYNTHASE INHIBITORS<br/>[FR] INHIBITEURS DE L'ACIDE GRAS SYNTHASE
    申请人:GLAXOSMITHKLINE LLC
    公开号:WO2012037298A1
    公开(公告)日:2012-03-22
    This invention relates to the use of imidazole, triazole, and tetrazole derivatives for the modulation, notably the inhibition of the activity or function of fatty acid synthase (FAS). Suitably, the present invention relates to the use of imidazoles, triazoles, and tetrazoles in the treatment of cancer.
    这项发明涉及使用咪唑、三唑和四唑衍生物来调节,尤其是抑制脂肪酸合酶(FAS)的活性或功能。适当地,本发明涉及在癌症治疗中使用咪唑、三唑和四唑。
  • Substituted Benzo-Imidazo-Pyrido-Diazepine Compounds
    申请人:Ashwell Mark A.
    公开号:US20120108574A1
    公开(公告)日:2012-05-03
    The present invention relates to substituted benzo-imidazo-pyrido-diazepine compounds and methods of synthesizing these compounds. The present invention also relates to pharmaceutical compositions containing substituted benzo-imidazo-pyrido-diazepine compounds and methods of treating cell proliferative disorders, such as cancer, by administering these compounds and pharmaceutical compositions to subjects in need thereof.
    本发明涉及取代的苯并咪唑吡啶二氮杂化合物及其合成方法。本发明还涉及含有取代的苯并咪唑吡啶二氮杂化合物的药物组合物,以及通过向需要的主体施用这些化合物和药物组合物来治疗细胞增殖性障碍,如癌症的方法。
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