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2-溴-6-氟苯甲醇 | 261723-33-5

中文名称
2-溴-6-氟苯甲醇
中文别名
2-氟-6-溴苯甲醇;2-氟-6-溴苄醇
英文名称
(2-bromo-6-fluorophenyl)methanol
英文别名
——
2-溴-6-氟苯甲醇化学式
CAS
261723-33-5
化学式
C7H6BrFO
mdl
——
分子量
205.026
InChiKey
HHGJENWYHVFPSA-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:
    256.7±25.0 °C(Predicted)
  • 密度:
    1.658±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    1.7
  • 重原子数:
    10
  • 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:
    20.2
  • 氢给体数:
    1
  • 氢受体数:
    2

安全信息

  • 海关编码:
    2906299090
  • 危险性防范说明:
    P261,P305+P351+P338
  • 危险性描述:
    H302,H315,H319,H335
  • 储存条件:
    室温且干燥环境下使用。

SDS

SDS:a3e860bb76a1cf45694dd63b4aef2a71
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Material Safety Data Sheet

Section 1. Identification of the substance
Product Name: 2-Bromo-6-fluorobenzyl alcohol
Synonyms: (2-Bromo-6-fluorophenyl)methanol

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

Section 3. Composition/information on ingredients.
Ingredient name: 2-Bromo-6-fluorobenzyl alcohol
CAS number: 261723-33-5

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: C7H6BrFO
Molecular weight: 205.0

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, hydrogen bromide.

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

制备方法与用途

2-溴-6-氟苯甲醇是一种重要的医药中间体,广泛用于制药领域。

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:
    2-溴-6-氟苯甲醇吡啶三溴化磷 作用下, 以 氯仿 为溶剂, 以83%的产率得到2-氟-6-溴溴苄
    参考文献:
    名称:
    MINERALOCORTICOID RECEPTOR ANTAGONISTS AND METHODS OF USE
    摘要:
    本发明提供了一种式(I)化合物: 或其药学上可接受的盐;包含式(I)化合物与适宜载体、稀释剂或赋形剂的药物组合物;以及治疗生理障碍,特别是充血性心力衰竭、高血压、糖尿病肾病或慢性肾病的方法,包括给予式(I)化合物或其药学上可接受的盐。
    公开号:
    US20090163472A1
  • 作为产物:
    描述:
    2-溴-6-氟苯甲醛甲醇 、 sodium tetrahydroborate 作用下, 生成 2-溴-6-氟苯甲醇
    参考文献:
    名称:
    中断束缚双烯酮的科里-柴可夫斯基反应以获得 2,3-环氧-六氢芴-9-酮
    摘要:
    Corey-Chaykovsky 反应通常用于从活化烯烃合成环丙烷。我们截取了这一转化过程中盛行的中间体,并改变了创建复杂分子基序的过程。我们描述了通过“中断的科里-柴可夫斯基反应”将束缚双烯酮转化为 2,3-环氧-六氢芴-9-酮的不寻常的骨架重塑。该策略合理地将硫叶立德的亲核特性与电子偏压烯烃相结合,以实现几种新型氢芴酮的区域和立体选择性合成。我们已经证明了该产品在获得几种高度功能化分子方面的合成效用。
    DOI:
    10.1021/acs.orglett.4c01550
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文献信息

  • POLYSUBSTITUTED DERIVATIVES OF 2-HETEROARYL-6-PHENYLIMIDAZO[1,2-a]PYRIDINES, AND PREPARATION AND THERAPEUTIC USE THEREOF
    申请人:DE PERETTI Danielle
    公开号:US20110065727A1
    公开(公告)日:2011-03-17
    Compounds of formula (I): wherein R, R 1 , R 2 , R 3 , R 4 and X are as defined in the disclosure, or an acid addition salt thereof, and the therapeutic use and process of synthesis thereof.
    式(I)的化合物: 其中R、R1、R2、R3、R4和X如披露中所定义,或其酸盐,以及其治疗用途和合成过程。
  • [EN] TETRAZOLINONE COMPOUNDS AND ITS USE AS PESTICIDES<br/>[FR] COMPOSÉS DE TÉTRAZOLINONE ET LEUR UTILISATION EN TANT QUE PESTICIDES
    申请人:SUMITOMO CHEMICAL CO
    公开号:WO2013162072A1
    公开(公告)日:2013-10-31
    The present invention provides a compound having an excellent efficacy for controlling pests. A tetrazolinone compound of a formula (1): [wherein R1 represents an C6-C16 aryl group, an C1-C12 alkyl group, or a C3-C12 cycloalkyl group, etc., which each optionally be substituted; R2, R3, R4 and R5 represent independently of each other a hydrogen atom, a halogen atom or an C1-C3 alkyl group, etc.; R6 represents an C1-C6 alkyl group, a C3-C6 cycloalkyl group, a halogen atom, a C1-C6 haloalkyl group, an C2-C6 alkenyl group, an C1-C6 alkoxy group, or a C1-C6 haloalkoxy group, etc.; R7, R8 and R9 represent independently of each other a hydrogen atom, a halogen atom, or an C1-C4 alkyl group, etc.; X represents an oxygen atom or a sulfur atom; and R10 represents an C1-C6 alkyl group, etc.] shows an excellent controlling efficacy on pests.
    本发明提供了一种具有优异杀虫效果的化合物。公式(1)的四唑酮化合物:[其中R1代表C6-C16芳基、C1-C12烷基或C3-C12环烷基等,每个都可以选择性地被取代;R2、R3、R4和R5分别独立地代表氢原子、卤素原子或C1-C3烷基等;R6代表C1-C6烷基、C3-C6环烷基、卤素原子、C1-C6卤代烷基、C2-C6烯基、C1-C6烷氧基或C1-C6卤代烷氧基等;R7、R8和R9分别独立地代表氢原子、卤素原子或C1-C4烷基等;X代表氧原子或原子;R10代表C1-C6烷基等]在杀虫方面表现出优异的控制效果。
  • POLYSUBSTITUTED DERIVATIVES OF 2-ARYL-6-PHENYL-IMIDAZO[1,2-a]PYRIDINES, AND PREPARATION AND THERAPEUTIC USE THEREOF
    申请人:DE PERETTI Danielle
    公开号:US20110065699A1
    公开(公告)日:2011-03-17
    Compounds of formula (I): wherein R 1 , R 2 , R 3 , R 4 and X are as defined in the disclosure, or an acid addition salt thereof, and the therapeutic use and process of synthesis thereof.
    式(I)的化合物: 其中R1、R2、R3、R4和X如披露中所定义,或其酸盐加合物,以及其治疗用途和合成过程。
  • BENZENESULFONAMIDE COMPOUNDS AND THEIR USE AS THERAPEUTIC AGENTS
    申请人:Xenon Pharmaceuticals Inc.
    公开号:US20180162868A1
    公开(公告)日:2018-06-14
    This invention is directed to benzenesulfonamide compounds, as stereoisomers, enantiomers, tautomers thereof or mixtures thereof; or pharmaceutically acceptable salts, solvates or prodrugs thereof, for the treatment of diseases or conditions associated with voltage-gated sodium channels, such as epilepsy and/or epileptic seizure disorders.
    这项发明涉及苯磺酰胺化合物,作为其立体异构体、对映异构体、互变异构体或它们的混合物;或其药学上可接受的盐、溶剂合物或前药,用于治疗与电压门控通道相关的疾病或症状,如癫痫和/或癫痫发作障碍。
  • [EN] COMPOUNDS AND COMPOSITIONS FOR INHIBITING THE ACTIVITY OF HIF2-ALPHA AND THEIR METHODS OF USE<br/>[FR] COMPOSÉS ET COMPOSITIONS PERMETTANT D'INHIBER L'ACTIVITÉ DE HIF2-ALPHA ET LEURS PROCÉDÉS D'UTILISATION
    申请人:NOVARTIS AG
    公开号:WO2021220170A1
    公开(公告)日:2021-11-04
    The present invention relates to compounds of formula (I) or a pharmaceutically acceptable salt form thereof, wherein the substituents are as defined in the specification; to intermediates in the preparation of the compounds, to pharmaceutical compositions comprising the compounds and to the use of the compounds in the treatment of disease. The compounds are inhibitors or modulators of HIF2alpha.
    本发明涉及公式(I)的化合物或其药用可接受的盐形式,其中取代基如规范中所定义;制备该化合物的中间体;包含该化合物的药物组合物;以及利用该化合物治疗疾病。这些化合物是HIF2alpha的抑制剂或调节剂。
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