2-溴-5-甲氧基苯甲酸叔丁酯 | 957063-12-6

• 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: 2-溴-5-甲氧基苯甲酸叔丁酯
• 英文名称: 2-bromo-5-methoxybenzoic acid tert-butyl ester
• 英文别名: tert-Butyl 2-bromo-5-methoxybenzoate
• CAS: 957063-12-6
• 化学式: C₁₂H₁₅BrO₃
• 分子量: 287.153
• InChiKey: JNNMFVKQTXPGQD-UHFFFAOYSA-N

物化性质

• 沸点：
  325.8±22.0 °C(Predicted)
• 密度：
  1.322±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  3.4
• 重原子数：
  16
• 可旋转键数：
  4
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.42
• 拓扑面积：
  35.5
• 氢给体数：
  0
• 氢受体数：
  3

安全信息

• 危险品标志：
  Xi
• 海关编码：
  2918990090

SDS

Material Safety Data Sheet

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Section 1. Identification of the substance
Product Name: tert-Butyl 2-bromo-5-methoxybenzoate
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: tert-Butyl 2-bromo-5-methoxybenzoate
CAS number: 957063-12-6

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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: C12H15BrO3
Molecular weight: 287.2

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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 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：

  2-溴-5-甲氧基苯甲酸叔丁酯 在 palladium on activated charcoal 、 palladium diacetate 、 N,N-二甲基甲酰胺 三乙基硅烷 、 草酰氯 、 potassium tert-butylate 、 氢气 、 三乙胺 、 三(邻甲基苯基)磷 、 三氟乙酸 作用下， 以 四氢呋喃 、 1,4-二氧六环 、 乙醇 、 二氯甲烷 、 甲苯 为溶剂， 反应 56.0h， 生成 3-(2-{(S)-2-[4-(4-Cyclohexyl-butylcarbamoyl)-oxazol-2-yl]-pyrrolidine-1-carbonyl}-4-methoxy-phenyl)-propionic acid ethyl ester
  参考文献：
  名称：

  FATTY ACID AMIDE HYDROLASE INHIHIBITORS FOR TREATING PAIN

  摘要：

  本文描述了化学式1的化合物。这些化合物可用于治疗患有疼痛或其他由FAAH介导的疾病的患者。

  公开号：

  US20120270915A1
• 作为产物：
  描述：

  2-溴-5-甲氧基苯甲酸 在 N,N-二甲基甲酰胺 草酰氯 作用下， 以 四氢呋喃 、 甲苯 为溶剂， 反应 17.0h， 生成 2-溴-5-甲氧基苯甲酸叔丁酯
  参考文献：
  名称：

  FATTY ACID AMIDE HYDROLASE INHIHIBITORS FOR TREATING PAIN

  摘要：

  本文描述了化学式1的化合物。这些化合物可用于治疗患有疼痛或其他由FAAH介导的疾病的患者。

  公开号：

  US20120270915A1

文献信息

• A unified synthesis of cyclic ethers or lactones via Pd-catalyzed intramolecular O -functionalization of sp 3 C H bonds
  作者：Haifeng Wang、Youhong Niu、Guoying Zhang、Xin-Shan Ye

  DOI：10.1016/j.tetlet.2016.08.086

  日期：2016.10

  via Pd-catalyzed C(sp3)H activation and intramolecular CO functionalization starting from carboxylic acids or alcohols using the bidentate directing group has been developed. Substrates with both primary and secondary hydroxyl groups can undergo this reaction to produce the corresponding cyclic ethers. Furthermore, isobenzofuran-1(3H)-ones with either electron-rich or electron-deficient groups as well

  已经开发了通过使用二齿指导基团从羧酸或醇开始的Pd催化的C（sp 3）H活化和分子内C O官能化来合成内酯或环状醚的一般方法。具有伯羟基和仲羟基的底物都可以进行此反应，以产生相应的环状醚。此外，通过使用该反应，可以制备具有富电子基团或缺乏电子基团的异苯并呋喃-1（3 H）-酮以及脂肪族内酯。
• Closing the Cycle as It Begins: Synthesis of <i>ortho</i> ‐Iodobiaryls via Catellani Reaction
  作者：Vinayak Botla、Marco Fontana、Aleksandr Voronov、Raimondo Maggi、Elena Motti、Giovanni Maestri、Nicola Della Ca'

  DOI：10.1002/anie.202218928

  日期：——

  A new strategy based on the Catellani reactions has enabled the one-pot synthesis of ortho-iodobiaryls starting from aryl iodides and bromides. Beyond the synthetic utility of this transformation (32 examples and 6 subsequent derivatizations), a DFT study provides insights on the mechanism of the reductive elimination step, which is driven by an original transmetallation between palladium(II)-halide

  一种基于Catellani 反应的新策略使得能够从芳基碘化物和芳基溴化物开始一锅法合成邻碘二芳基化合物。除了这种转化的综合效用（32 个例子和 6 个后续衍生化）之外，DFT 研究还提供了对还原消除步骤机制的见解，该步骤由钯 (II)-卤化物络合物之间的原始金属转移作用驱动。
• FATTY ACID AMIDE HYDROLASE INHIBITORS FOR TREATING PAIN
  申请人：Allergan, Inc.

  公开号：EP2699565A1

  公开（公告）日：2014-02-26
• [EN] FATTY ACID AMIDE HYDROLASE INHIBITORS FOR TREATING<br/>[FR] INHIBITEURS DE L'HYDROLASE D'AMIDE D'ACIDE GRAS (FAAH) POUR ADMINISTRER UN TRAITEMENT
  申请人：ALLERGAN INC

  公开号：WO2012145737A1

  公开（公告）日：2012-10-26

  Compounds of Formula 1 are described herein. These compounds may be administered to a patient for treatment of suffering from pain or other FAAH mediated conditions.