3-异丁氨基羰基苯硼酸 | 723282-09-5

• 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-异丁氨基羰基苯硼酸
• 中文别名: 3-(异丁基氨甲酰基)苯硼酸
• 英文名称: [3-(ISOBUTYLAMINOCARBONYL)PHENYL]BORONIC ACID
• 英文别名: 3-(Isobutylaminocarbonyl)phenylboronic acid；[3-(2-methylpropylcarbamoyl)phenyl]boronic acid
• CAS: 723282-09-5
• 化学式: C₁₁H₁₆BNO₃
• mdl: MFCD04115692
• 分子量: 221.064
• InChiKey: VRCFUCPIPJUGKG-UHFFFAOYSA-N

物化性质

• 熔点：
  224-230
• 密度：
  1.13±0.1 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  1.75
• 重原子数：
  16
• 可旋转键数：
  4
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.363
• 拓扑面积：
  69.6
• 氢给体数：
  3
• 氢受体数：
  3

安全信息

• 危险品标志：
  Xi
• 海关编码：
  2931900090

SDS

Material Safety Data Sheet

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

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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

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Section 3. Composition/information on ingredients.
3-(Isobutylaminocarbonyl)phenylboronic acid
Ingredient name:
CAS number: 723282-09-5

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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:

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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.
Storage: Store in closed vessels.

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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
Not specified
Appearance:
Boiling point: No data
Melting point: No data
Flash point: No data
Density: No data
Molecular formula: C11H16BNO3
Molecular weight: 221.1

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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.

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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：

  1,2,3-三碘苯 、 3-异丁氨基羰基苯硼酸 在 四(三苯基膦)钯 、 potassium carbonate 作用下， 以 乙醇 、 甲苯 为溶剂， 反应 12.0h， 以54%的产率得到2',3'-diiodo-N-isobutyl-[1,1'-biphenyl]-3-carboxamide
  参考文献：
  名称：

  通过 5-取代 1,2,3-三碘苯的区域选择性 Suzuki-Miyaura 交叉偶联反应合成二碘联苯和碘化间三联苯

  摘要：

  通过 5-取代的 1,2,3-三碘苯的区域选择性 Suzuki-Miyaura 交叉偶联反应合成了多种 2,3-二碘化联苯和碘化间三联苯衍生物。通过使用 1 当量。Suzuki-Miyaura 反应生成了具有优异区域选择性的 2,3-二碘化联苯衍生物。偶联反应主要发生在 5-取代的 1,2,3-三碘苯的末端位置，这是空间位阻较小且电子缺陷较多的位点。2当量。芳基硼酸，一锅反应以良好的产率提供碘化的间三联苯。这种简便高效的一步法在范围和可扩展性方面也非常通用。

  DOI：

  10.1002/ejoc.201500263

文献信息

• Synthesis of Diiodinated Biphenyls and Iodinated<i>meta</i>-Terphenyls by Regioselective Suzuki-Miyaura Cross-Coupling Reactions of 5-Substituted 1,2,3-Triiodobenzenes
  作者：Raed M. Al-Zoubi、Walid K. Al-Jammal、Mohammad Y. El-Khateeb、Robert McDonald

  DOI：10.1002/ejoc.201500263

  日期：2015.5

  were synthesized by a regioselective Suzuki–Miyaura cross-coupling reaction of 5-substituted 1,2,3-triiodobenzenes. By using 1 equiv. of arylboronic acid, the Suzuki–Miyaura reaction yielded 2,3-diiodinated biphenyl derivatives with excellent regioselectivity. The coupling reaction predominantly occurred at the terminal position of the 5-substituted 1,2,3-triiodobenzene, which is the less sterically

  通过 5-取代的 1,2,3-三碘苯的区域选择性 Suzuki-Miyaura 交叉偶联反应合成了多种 2,3-二碘化联苯和碘化间三联苯衍生物。通过使用 1 当量。Suzuki-Miyaura 反应生成了具有优异区域选择性的 2,3-二碘化联苯衍生物。偶联反应主要发生在 5-取代的 1,2,3-三碘苯的末端位置，这是空间位阻较小且电子缺陷较多的位点。2当量。芳基硼酸，一锅反应以良好的产率提供碘化的间三联苯。这种简便高效的一步法在范围和可扩展性方面也非常通用。