3-氟-联苯-2-羧酸 | 2094-03-3

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 中文名称: 3-氟-联苯-2-羧酸
• 中文别名: 3'-氟-[1,1'-联苯]-2-羧酸
• 英文名称: 3'-fluoro-[1,1'-biphenyl]-2-carboxylic acid
• 英文别名: 2-(3-fluoro)phenylbenzoic acid；3'-fluoro-biphenyl-2-carboxylic acid；3'-Fluor-2-biphenylcarbonsaeure；2-(3-fluorophenyl)benzoic Acid
• CAS: 2094-03-3
• 化学式: C₁₃H₉FO₂
• 分子量: 216.212
• InChiKey: GEZNPQHOTCPFEL-UHFFFAOYSA-N

物化性质

• 沸点：
  344.7±17.0 °C(Predicted)
• 密度：
  1.261±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  3
• 重原子数：
  16
• 可旋转键数：
  2
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  37.3
• 氢给体数：
  1
• 氢受体数：
  3

安全信息

• 危险品标志：
  Xi
• 海关编码：
  2916399090

SDS

Material Safety Data Sheet

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

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

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Section 3. Composition/information on ingredients.
Ingredient name: 2-(3-Fluorophenyl)benzoic acid
CAS number: 2094-03-3

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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.

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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.

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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.

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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:

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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.

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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: C13H9FO2
Molecular weight: 216.2

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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.

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Section 11. Toxicological information
No data.

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Section 12. Ecological information
No data.

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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.

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Section 14. Transportation information
Non-harzardous for air and ground transportation.

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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.

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SECTION 16 - ADDITIONAL INFORMATION
N/A

反应信息

• 作为反应物：
  描述：

  3-氟-联苯-2-羧酸 在 dipotassium peroxodisulfate 、 氧气 作用下， 以 水 、 乙腈 为溶剂， 以81%的产率得到2-fluoro-6H-benzo[c]chromen-6-one
  参考文献：
  名称：

  芳烃的通用和实用的羧基定向远程 C?H 氧化反应

  摘要：

  已经开发了两种用于远程芳族 C  H 氧化反应的方法。方法 1，即 Cu 催化的氧化反应，对于将电子中性和富电子的联芳基羧酸环化为 3,4-苯香豆素非常有效。方法 2，K 2 S 2 O 8介导的氧化反应，对于具有给电子和吸电子基团的底物的环化更为通用和实用（见方案）。

  DOI：

  10.1002/chem.201303511
• 作为产物：
  描述：

  3-氟苯基硼酸 在 trans-bis(triphenylphosphine)palladium dichloride 、 sodium carbonate 、 sodium hydroxide 作用下， 以 四氢呋喃 、 甲醇 、 水 为溶剂， 反应 6.0h， 生成 3-氟-联苯-2-羧酸
  参考文献：
  名称：

  Pd催化的C–H漆基化方便地合成联芳基内酯和总合成大麻酚

  摘要：

  已开发出一种实用的Pd（II）/ Pd（IV）催化的羧基定向C–H活化/ C–O环化反应来构建联芳基内酯。该新反应的合成效用在天然经济的大麻素从市售原料中进行了原子经济且操作方便的全合成中得到了证明，其中新开发的方法用于两个关键步骤。

  DOI：

  10.1021/ol400877q

文献信息

• [EN] DISUBSTITUTED OCTAHY-DROPYRROLO [3,4-C] PYRROLES AS OREXIN RECEPTOR MODULATORS<br/>[FR] OCTAHYDROPYRROLO [3,4-C] PYRROLES DISUBSTITUÉS UTILISÉS COMME MODULATEURS DU RÉCEPTEUR DE L'OREXINE
  申请人：JANSSEN PHARMACEUTICA NV

  公开号：WO2012145581A1

  公开（公告）日：2012-10-26

  Disubstituted octahydropyrrolo[3,4-c]pyrrole compounds are described, which are useful as orexin receptor modulators. Such compounds may be useful in pharmaceutical compositions and methods for the treatment of diseased states, disorders, and conditions mediated by orexin activity, such as insomnia.

  描述了二取代的八氢吡咯[3,4-c]吡咯化合物，这些化合物可用作促进睡眠素受体的调节剂。这些化合物可能在药物组合物和治疗由促进睡眠素活性介导的疾病状态、紊乱和病况的方法中有用，比如失眠。
• Cerium photocatalyzed dehydrogenative lactonization of 2-arylbenzoic acids
  作者：Ketan Wadekar、Suraj Aswale、Veera Reddy Yatham

  DOI：10.1039/c9ob02676b

  日期：——

  The first cerium photocatalyzed dehydrogenative lactonization of 2-arylbenzoic acids has been developed. This operationally simple protocol allows rapid access to synthetically useful coumarins on gram scale by employing CeCl3 as a photocatalyst and O2 as a terminal oxidant. Overall, this delivers an economical and environmentally amiable entry to diversely substituted coumarins, important structural

  已经开发出第一铈对2-芳基苯甲酸的光催化的脱氢内酯化。通过使用CeCl3作为光催化剂和O2作为末端氧化剂，这种操作简单的方案可以以克为单位快速获得合成有用的香豆素。总体而言，这为各种取代的香豆素提供了经济和环境友好的入口，香豆素是生物活性分子中的重要结构图案。
• Scalable Electrochemical Dehydrogenative Lactonization of C(sp²/sp³)–H Bonds
  作者：Sheng Zhang、Lijun Li、Huiqiao Wang、Qian Li、Wenmin Liu、Kun Xu、Chengchu Zeng

  DOI：10.1021/acs.orglett.7b03617

  日期：2018.1.5

  A practical, electrochemical method is developed for the direct dehydrogenative lactonization of C(sp2/sp3)–H bonds under external oxidant- and metal-free conditions, delivering diverse lactones, including coumarin derivatives with excellent regioselectivity. The scalable nature of this newly developed electrochemical process was demonstrated on a 40 g scale following an operationally simple protocol

  开发了一种实用的电化学方法，用于在无外部氧化剂和无金属的条件下对C（sp 2 / sp 3）–H键进行直接脱氢内酯化，从而提供多种内酯，包括具有优异区域选择性的香豆素衍生物。遵循操作简单的协议，以40 g规模展示了这种新开发的电化学过程的可扩展性。C（sp 3）-H键的远程内酯化将构成朝着电化学C-O键形成的重要合成进展。
• Organocatalytic Electrochemical C–H Lactonization of Aromatic Carboxylic Acids
  作者：Sanzhong Luo、Longji Li、Qi Yang、Zongbin Jia

  DOI：10.1055/s-0036-1591558

  日期：2018.8

  Radical Methods and their Strategic Applications in Synthesis Abstract An electrochemical strategy has been developed for radical arene carbon–oxygen bond formation. This reaction utilizes DDQ as a redox mediator, with inexpensive glassy carbon electrodes to facilitate an intramolecular lactonization of biphenyl-2-carboxylic acid derivatives via aromatic carboxyl radical substitution to give 6H-be

  §这些作者同等贡献。 作为特别主题“现代自由基方法及其在合成中的战略应用”的一部分发布 抽象的 已经开发出一种用于自由基芳烃碳-氧键形成的电化学策略。该反应利用DDQ作为氧化还原介体，并具有廉价的玻璃碳电极，以通过芳族羧基自由基取代促进联苯-2-羧酸衍生物的分子内内酯化，得到6 H-苯并[ c ] chromen-6-one。 已经开发出一种用于自由基芳烃碳-氧键形成的电化学策略。该反应利用DDQ作为氧化还原介体，并具有廉价的玻璃碳电极，以通过芳族羧基自由基取代促进联苯-2-羧酸衍生物的分子内内酯化，得到6 H-苯并[ c ] chromen-6-one。
• [EN] DISUBSTITUTED OCTAHY - DROPYRROLO [3,4-C] PYRROLES AS OREXIN RECEPTOR MODULATORS<br/>[FR] OCTAHYDROPYRROLO[3,4-C]PYRROLES DISUBSTITUÉS EN TANT QUE MODULATEURS DE RÉCEPTEUR D'OREXINE
  申请人：JANSSEN PHARMACEUTICA NV

  公开号：WO2011050198A1

  公开（公告）日：2011-04-28

  Disubstituted octahydropyrrolo[3,4-c]pyrrole compounds are described, which are useful as orexin receptor modulators. Such compounds may be useful in pharmaceutical compositions and methods for the treatment of diseased states, disorders, and conditions mediated by orexin activity, such as insomnia.

  描述了二取代的八氢吡咯并[3,4-c]吡咯化合物，这些化合物可用作促进睡眠素受体的调节剂。这些化合物可能在药物组合物和治疗由促进睡眠素活性介导的疾病状态、紊乱和症状的方法中有用，比如失眠。