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3-(2-羟基乙基)苯基硼酸 | 647853-32-5

中文名称
3-(2-羟基乙基)苯基硼酸
中文别名
3-(2-羟基乙基)苯硼酸
英文名称
[3-(2-hydroxyethyl)phenyl]boronic acid
英文别名
(3-(2-Hydroxyethyl)phenyl)boronic acid
3-(2-羟基乙基)苯基硼酸化学式
CAS
647853-32-5
化学式
C8H11BO3
mdl
MFCD03095123
分子量
165.985
InChiKey
GCSYFWQBJAJDGY-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

计算性质

  • 辛醇/水分配系数(LogP):
    1.06
  • 重原子数:
    12
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.25
  • 拓扑面积:
    60.7
  • 氢给体数:
    3
  • 氢受体数:
    3

安全信息

  • 危险品标志:
    Xi
  • 危险性防范说明:
    P261,P305+P351+P338
  • 危险性描述:
    H315,H319,H335

SDS

SDS:3b1b39293caf8d802fd990391335752d
查看
Material Safety Data Sheet

Section 1. Identification of the substance
3-(2-Hydroxyethyl)phenylboronic acid
Product Name:
Synonyms:

Section 2. Hazards identification
Harmful by inhalation, in contact with skin, and if swallowed.
H315: Causes skin irritation
H319: Causes serious eye irritation
H335: May cause respiratory irritation
P261: Avoid breathing dust/fume/gas/mist/vapours/spray
Wear protective gloves/protective clothing/eye protection/face protection
P280:
P305+P351+P338: IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses if present
and easy to do – continue rinsing
P304+P340: IF INHALED: Remove victim to fresh air and keep at rest in a position comfortable for breathing
P405: Store locked up

Section 3. Composition/information on ingredients.
3-(2-Hydroxyethyl)phenylboronic acid
Ingredient name:
CAS number: 647853-32-5

Section 4. First aid measures
Immediately wash skin with copious amounts of water for at least 15 minutes while removing
Skin contact:
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.
Wash out mouth with copious amounts of water for at least 15 minutes. Seek medical attention.
Ingestion:

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.
Storage: Store in closed vessels, refrigerated.

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
Not specified
Appearance:
Boiling point: No data
Melting point: No data
Flash point: No data
Density: No data
Molecular formula: C8H11BO3
Molecular weight: 166.0

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-(2-羟基乙基)苯基硼酸 在 Chiralcel OD 作用下, 以 甲醇乙醇正庚烷二氯甲烷N,N-二甲基甲酰胺甲苯乙腈 为溶剂, 反应 3.5h, 生成 (R)-5-(1-amino-isoquinolin-6-ylamino)-19-cyclopropanesulfonyl-3-methyl-13-oxa-3,15-diaza-tricyclo[14.3.1.16,10]henicosa-1(19),6(21),7,9,16(20),17-hexaene-4,14-dione trifluoroacetic acid salt
    参考文献:
    名称:
    新型Meta-linked苯甘氨酸大环FVIIa抑制剂的设计与合成
    摘要:
    已经设计了两种新颖的基于间联苯基苯甘氨酸的大环FVIIa抑制剂系列,以改善啮齿动物的代谢稳定性和前体对联苯基苯甘氨酸大环化合物所观察到的PK。通过基于迭代结构的设计和优化,TF / FVIIa K i被提高到亚纳摩尔水平,具有良好的凝结活性,代谢稳定性和通透性。
    DOI:
    10.1021/acsmedchemlett.6b00375
  • 作为产物:
    描述:
    3-溴苯乙醇咪唑正丁基锂 作用下, 以 四氢呋喃二氯甲烷 为溶剂, 反应 5.17h, 生成 3-(2-羟基乙基)苯基硼酸
    参考文献:
    名称:
    新型Meta-linked苯甘氨酸大环FVIIa抑制剂的设计与合成
    摘要:
    已经设计了两种新颖的基于间联苯基苯甘氨酸的大环FVIIa抑制剂系列,以改善啮齿动物的代谢稳定性和前体对联苯基苯甘氨酸大环化合物所观察到的PK。通过基于迭代结构的设计和优化,TF / FVIIa K i被提高到亚纳摩尔水平,具有良好的凝结活性,代谢稳定性和通透性。
    DOI:
    10.1021/acsmedchemlett.6b00375
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文献信息

  • [EN] 2-METHYL-QUINAZOLINES<br/>[FR] 2-MÉTHYL-QUINAZOLINES
    申请人:BAYER PHARMA AG
    公开号:WO2018172250A1
    公开(公告)日:2018-09-27
    The present invention describes 2-methyl-quinazoline compounds of general formula (I), 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. The 2-methyl substituted quinazoline compounds of general formula(I) effectively and selectively inhibit the Ras-Sos interaction without significantly targeting the EGFR receptor. They are therefore useful for the treatment or prophylaxis of diseases, in particular of hyperproliferative disorders, such as cancer as a sole agent or in combination with other active ingredients.
    本发明描述了一般式(I)的2-甲基喹唑啉化合物,制备该化合物的方法,用于制备该化合物的中间体化合物,包含该化合物的药物组合物和组合物,以及用于制造药物组合物的该化合物的用途。一般式(I)的2-甲基取代喹唑啉化合物有效且选择性地抑制Ras-Sos相互作用,而不显著靶向EGFR受体。因此,它们对于治疗或预防疾病特别是高增殖性疾病,如癌症作为单一药剂或与其他活性成分组合使用是有用的。
  • [EN] PHENOXYPYRIDINYLAMIDE DERIVATIVES AND THEIR USE IN THE TREATMENT OF PDE4 MEDIATED DISEASE STATES<br/>[FR] DÉRIVÉS DE PHÉNOXYPYRIDINYLAMIDE ET LEUR UTILISATION DANS LE TRAITEMENT D'ÉTATS PATHOLOGIQUES INDUITS PAR LA PHOSPHODIÉSTERASE 4 (PDE4)
    申请人:ASTRAZENECA AB
    公开号:WO2009144494A1
    公开(公告)日:2009-12-03
    The present invention provides a compound of a formula (I), wherein the variables are defined herein; to a process for preparing such a compound; and to the use of such a compound in the treatment of a PDE4 mediated disease state.
    本发明提供了一种化合物的公式(I),其中变量在此定义;以及制备这种化合物的方法;以及在治疗PDE4介导的疾病状态中使用这种化合物。
  • [EN] ARYL AND ARYLALKYL SUBSTITUTED PYRAZOLYL AND PYRIMIDINYL TRICYCLIC ENONES AS ANTIOXIDANT INFLAMMATION MODULATORS<br/>[FR] PYRAZOLYLE SUBSTITUÉ PAR UN ARYLE ET ARYLALKYLE ET PYRIMIDINYL ÉNONES TRICYCLIQUES COMME MODULATEURS ANTIOXYDANTS DE L'INFLAMMATION
    申请人:ABBVIE INC
    公开号:WO2015112792A1
    公开(公告)日:2015-07-30
    The present application relates to: (a) compounds of Formula (I): and salts thereof, wherein R1, R2, R3, R4, R5, R6, m, n, X and Y are as defined in the specification; (b) compositions comprising such compounds and salts; and (c) methods of use of such compounds, salts, and compositions, particularly use for the treatment and prevention of diseases such as those associated with oxidative stress and inflammation.
    本申请涉及:(a) 公式(I)的化合物及其盐,其中R1、R2、R3、R4、R5、R6、m、n、X和Y如规范中所定义;(b) 包含这些化合物和盐的组合物;以及(c) 使用这些化合物、盐和组合物的方法,特别是用于治疗和预防与氧化应激和炎症相关的疾病。
  • N-myristoyl transferase inhibitors
    申请人:Brand Stephen
    公开号:US09156811B2
    公开(公告)日:2015-10-13
    The present invention relates to N-heterocyclic sulphonamide compounds, in particular pyrazole sulphonamide compounds, and their use as N-myristoyl transferase inhibitors.
    本发明涉及N-杂环磺胺化合物,特别是吡唑磺胺化合物,以及它们作为N-肟酰基转移酶抑制剂的用途。
  • [EN] CHROMENONE INHIBITORS OF MONOCARBOXYLATE TRANSPORTERS<br/>[FR] INHIBITEURS CHROMÉNONE DE TRANSPORTEURS DE MONOCARBOXYLATE
    申请人:SCRIPPS RESEARCH INST
    公开号:WO2016118822A1
    公开(公告)日:2016-07-28
    The invention provides compounds effective as inhibitors of monocarboxylate transporters such as MCT1 and MCT4, which can be used for treatment of medical conditions wherein treatment of the condition with a compound having an inhibitor effect on MCT1, MCT4, or both is medically indicated. Compounds of the invention can have antitumor, antidiabetes, anti-inflammatory, or immunosuppressive pharmacological effects, and can be effective for treatment of cancer and of type II diabetes.
    该发明提供了作为单羧酸转运体抑制剂有效的化合物,如MCT1和MCT4,可用于治疗需要使用对MCT1、MCT4或两者都具有抑制剂作用的化合物进行治疗的医疗状况。该发明的化合物可以具有抗肿瘤、抗糖尿病、抗炎症或免疫抑制药理作用,并可有效用于治疗癌症和2型糖尿病。
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