3-溴-n-环己基苯甲酰胺 | 59507-55-0

• 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-溴-n-环己基苯甲酰胺
• 英文名称: 3-bromo-N-cyclohexylbenzamide
• 英文别名: m-Brombenzoylcyclohexylamid
• CAS: 59507-55-0
• 化学式: C₁₃H₁₆BrNO
• mdl: MFCD00554081
• 分子量: 282.18
• InChiKey: VRUMXGVWUFXLAH-UHFFFAOYSA-N

物化性质

• 熔点：
  166-168°C
• 沸点：
  402.1±28.0 °C(Predicted)
• 密度：
  1.37±0.1 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  3.7
• 重原子数：
  16
• 可旋转键数：
  2
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.461
• 拓扑面积：
  29.1
• 氢给体数：
  1
• 氢受体数：
  1

安全信息

• 危险品标志：
  Xi
• 海关编码：
  2924299090

SDS

Material Safety Data Sheet

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Section 1. Identification of the substance
Product Name: N-Cyclohexyl 3-bromobenzamide
Synonyms: 3-Bromo-N-cyclohexylbenzamide

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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: N-Cyclohexyl 3-bromobenzamide
CAS number: 59507-55-0

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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: C13H16BrNO
Molecular weight: 282.2

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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, nitrogen oxides, hydrogen bromide.

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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：

  对碘苯甲酸乙酯 、 3-溴-n-环己基苯甲酰胺 在 palladium diacetate silver(I) acetate 、 三氟乙酸 作用下， 反应 2.0h， 生成
  参考文献：
  名称：

  Carbon−Hydrogen Bond Functionalization Approach for the Synthesis of Fluorenones and ortho-Arylated Benzonitriles

  摘要：

  A sequence consisting of palladium-catalyzed benzamide ortho-arylation/reaction with (CF3CO)(2)O was developed allowing a convenient one-pot synthesis of ortho-arylated benzonitriles and fluorenone derivatives. The outcome of this transformation is dependent on the amide N-alkyl substituent. Dehydration of ortho-arylated N-cyclohexyl-benzamides by (CF3CO)(2)O results in efficient production of benzonitriles. In contrast, o-arylated N-propylbenzamides are converted to fluorenone derivatives.

  DOI：

  10.1021/jo801300y
• 作为产物：
  描述：

  3-溴苯甲酰氯 、 环己胺 在 三乙胺 作用下， 以 二氯甲烷 为溶剂， 反应 2.0h， 以95%的产率得到3-溴-n-环己基苯甲酰胺
  参考文献：
  名称：

  AMINE DERIVATIVE COMPOUNDS FOR TREATING OPHTHALMIC DISEASES AND DISORDERS

  摘要：

  提供的是胺衍生物化合物、其药物组合物，以及使用所述化合物和组合物治疗眼科疾病和障碍的方法，例如年龄相关的黄斑变性和斯达格特病。

  公开号：

  US20160193181A1

文献信息

• Pd(ii)-catalyzed decarboxylative cross-coupling of oxamic acids with potassium phenyltrifluoroborates under mild conditions
  作者：Mingzong Li、Cong Wang、Ping Fang、Haibo Ge

  DOI：10.1039/c1cc11635e

  日期：——

  A novel Pd-catalyzed decarboxylative cross-coupling of oxamic acids with potassium phenyltrifluoroborates has been realized under mild reaction conditions. This method provides an efficient access to N-mono- or N,N-disubstituted benzamides and benzoates.

  在温和反应条件下，实现了钯催化下的草氨酸与苯基三氟硼酸钾的去羧偶联反应。该方法为制备N-单取代或N,N-双取代苯甲酰胺和苯甲酸酯提供了高效的途径。
• Amine Derivative Compounds for Treating Ophthalmic Diseases and Disorders
  申请人：Scott Ian L.

  公开号：US20090281149A1

  公开（公告）日：2009-11-12

  Provided are amine derivative compounds, pharmaceutical compositions thereof, and methods of treating ophthalmic diseases and disorders, such as age-related macular degeneration and Stargardt's Disease, using said compounds and compositions.

  本发明涉及一种胺衍生物化合物，其制备的药物组合物以及使用该化合物和组合物治疗眼科疾病和障碍的方法，例如老年性黄斑变性和Stargardt病。
• Amine derivative compounds for treating ophthalmic diseases and disorders
  申请人：Acucela, Inc.

  公开号：US08076516B2

  公开（公告）日：2011-12-13

  Provided are amine derivative compounds, pharmaceutical compositions thereof, and methods of treating ophthalmic diseases and disorders, such as age-related macular degeneration and Stargardt's Disease, using said compounds and compositions.

  提供了氨基衍生物化合物、其药物组合物，以及使用该化合物和组合物治疗眼科疾病和疾病的方法，例如与年龄相关的黄斑退化和Stargardt病。
• ACYLATION REACTION OF HYDROXYL GROUP
  申请人：Mashima Kazushi

  公开号：US20100249422A1

  公开（公告）日：2010-09-30

  Disclosed is a selective ester production process of an alcoholic hydroxyl group, which proceeds under chemically mild conditions, while having adequate environmental suitability, operability and economical efficiency. Specifically disclosed is a process for producing an ester compound, which is characterized in that an alcohol and a carboxylic acid ester compound are reacted in the presence of a compound containing zinc element, thereby selectively acylating a hydroxyl group of the alcohol.

  公开了一种选择性酯化醇羟基的生产过程，该过程在化学上温和的条件下进行，同时具有足够的环境适应性、操作性和经济效益。具体公开了一种生产酯化合物的方法，其特征在于，在含锌元素的化合物存在下，将醇和羧酸酯化合物反应，从而选择性地酰化醇的羟基。
• Radical mediated-direct conversion of aldehydes into acid bromides
  作者：Dong Ho Kang、Tae Young Joo、Warinthorn Chavasiri、Doo Ok Jang

  DOI：10.1016/j.tetlet.2006.11.013

  日期：2007.1

  A method of preparing acid bromides directly from aldehydes with Br3CCO2Et under radical conditions was developed. Aromatic aldehydes with electron-donating group were found to be more reactive than aromatic aldehydes with electron-withdrawing group and aliphatic aldehydes under reaction conditions. (c) 2006 Elsevier Ltd. All rights reserved.