2-溴-4-碘苯胺 | 29632-73-3

• 物质功能分类: 有机原料 - 氨基化合物
• 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-4-碘苯胺
• 英文名称: 2-Bromo-4-iodoaniline
• CAS: 29632-73-3
• 化学式: C₆H₅BrIN
• mdl: MFCD07780668
• 分子量: 297.921
• InChiKey: HHWOYRKNRZSNQE-UHFFFAOYSA-N

物化性质

• 熔点：
  75-76 °C
• 沸点：
  307.6±32.0 °C(Predicted)
• 密度：
  2.292

计算性质

• 辛醇/水分配系数(LogP)：
  2.6
• 重原子数：
  9
• 可旋转键数：
  0
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  26
• 氢给体数：
  1
• 氢受体数：
  1

安全信息

• 海关编码：
  2921420090
• 危险性防范说明：
  P261,P305+P351+P338
• 危险性描述：
  H302,H315,H319,H335

SDS

Material Safety Data Sheet

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Section 1. Identification of the substance
Product Name: 2-Bromo-4-iodoaniline
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-Bromo-4-iodoaniline
CAS number: 29632-73-3

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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, refrigerated.
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: C6H5BrIN
Molecular weight: 297.9

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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, hydrogen Iodide.

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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-4-碘苯胺 在 亚硝酸特丁酯 、 三氟化硼乙醚 、 sodium iodide 作用下， 以 乙腈 为溶剂， 以68%的产率得到2-溴-1,4-二碘苯
  参考文献：
  名称：

  Synthesis of a single-molecule nanotruck

  摘要：

  We report the synthesis of a new nanovehicle, a porphyrin-based nanotruck. The porphyrin inner core was designed for possible transportation of metals and small molecules across a surface. (c) 2007 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tetlet.2007.06.081
• 作为产物：
  描述：

  N-(4-碘苯基)乙酰胺 在 盐酸 、 乙醇 、 水 、 氢溴酸 、 硝酸 作用下， 生成 2-溴-4-碘苯胺
  参考文献：
  名称：

  Heisig, Journal of the American Chemical Society, 1928, vol. 50, p. 143

  摘要：

  DOI：

文献信息

• Lewis Acid-Promoted Synthesis of Unsymmetrical and Highly Functionalized Carbazoles and Dibenzofurans from Biaryl Triazenes: Application for the Total Synthesis of Clausine C, Clausine R, and Clauraila A
  作者：Weijun Yang、Jun Zhou、Binjie Wang、Hongjun Ren

  DOI：10.1002/chem.201102802

  日期：2011.12.2

  A natural approach: A Lewis acid‐promoted nucleophilic aromatic substitution approach to the regioselective synthesis of highly substituted carbazoles and dibenzofurans has been developed. The annulation process is applied to the total synthesis of carbazole alkaloids clausine C, clausine R, and clauraila A (see scheme).

  一种自然方法：已开发出一种路易斯酸促进的亲核芳族取代方法，用于高度取代的咔唑和二苯并呋喃的区域选择性合成。环化工艺应用于咔唑生物碱克劳斯汀C，克劳斯汀R和克劳拉艾拉A的全合成（请参阅方案）。
• Iodination of anilines and phenols with 18-crown-6 supported ICl2−
  作者：Hannah W. Mbatia、Olbelina A. Ulloa、Daniel P. Kennedy、Christopher D. Incarvito、Shawn C. Burdette

  DOI：10.1039/c0ob00926a

  日期：——

  A highly crystalline iodinating reagent, [K·18-C-6]ICl2}n, was synthesized in high yield (93%). The trihalide is supported by an 18-crown-6 macrocycle and forms a coordination polymer in the solid state. This reagent iodinates anilines and phenols efficiently under mild conditions. Controlled mono-iodination with anilines was easily achieved while poly-iodination was observed with phenols.

  高结晶性的碘化试剂[K·18-C-6]ICl2}n以高产率（93%）合成。该三卤化物由18-冠-6大环支撑，并在固态下形成配位聚合物。该试剂在温和条件下高效碘化苯胺和酚。通过苯胺实现了可控的单碘化，而酚则观察到多碘化作用。
• Regioselective iodination of aryl amines using 1,4-dibenzyl-1,4-diazoniabicyclo [2.2.2] octane dichloroiodate in solution and under solvent-free conditions
  作者：M. Alikarami、S. Nazarzadeh、M. Soleiman-Beigi

  DOI：10.4314/bcse.v29i1.15

  日期：——

  1,4-Dibenzyl-1,4-diazoniabicyclo[2.2.2]octane dichloroiodate is an efficient and regioselective reagent for iodination of aryl amines. A wide variety of aryl amines in reaction with this reagent afforded regioselectively iodinated products. The iodination reaction can be carried out in solution or under solvent-free condition at room temperature.

  1,4-二苄基-1,4-二氮鎓二环[2.2.2]辛烷二氯碘酸盐是一种高效的区域选择性碘化试剂，适用于芳香胺的碘化反应。多种芳香胺与该试剂反应，均能区域选择性地生成碘化产物。该碘化反应可以在室温下于溶液中或无溶剂条件下进行。
• Mild and regioselective oxidative bromination of anilines using potassium bromide and sodium perborate
  作者：Didier Roche、Kapa Prasad、Oljan Repic、Thomas J Blacklock

  DOI：10.1016/s0040-4039(00)00119-2

  日期：2000.3

  The selective monobromination of various deactivated anilines using potassium bromide and sodium perborate as oxidant has been achieved. The use of ammonium molybdate as catalyst accelerates the rate of reaction but is not essential to obtain good yields and high selectivities.

  已经实现了使用溴化钾和过硼酸钠作为氧化剂对各种失活的苯胺的选择性单溴化。使用钼酸铵作为催化剂可以加快反应速度，但对于获得良好的收率和高选择性并不是必不可少的。
• Inhibitors of factor Xa
  申请人：Cor Therapeutics, Inc.

  公开号：US06399627B1

  公开（公告）日：2002-06-04

  Novel compounds, their salts and compositions related thereto having activity against mammalian factor Xa are disclosed. The compounds are useful in vitro or in vivo for preventing or treating coagulation disorders.

  披露了新型化合物、它们的盐和与它们相关的组合物，这些化合物对哺乳动物因子Xa具有活性。这些化合物在体外或体内用于预防或治疗凝血障碍。