2-溴-N-甲基苯胺盐酸盐 | 957120-69-3

• 分子结构分类: 有机化合物 - 有机氮化合物
• 中文名称: 2-溴-N-甲基苯胺盐酸盐
• 英文名称: N-methyl-2-bromoaniline hydrochloride
• 英文别名: 2-Bromo-N-methylaniline hydrochloride；2-bromo-N-methylaniline;hydrochloride
• CAS: 957120-69-3
• 化学式: C₇H₈BrN*ClH
• 分子量: 222.512
• InChiKey: BXUFFBPLMGZFJO-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.91
• 重原子数：
  10
• 可旋转键数：
  1
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.14
• 拓扑面积：
  12
• 氢给体数：
  2
• 氢受体数：
  1

安全信息

• 海关编码：
  2921420090

SDS

Material Safety Data Sheet

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Section 1. Identification of the substance
Product Name: 2-Bromo-N-methylaniline, HCl
Synonyms: N-Methyl 2-bromoaniline, HCl

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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-N-methylaniline, HCl
CAS number: 957120-69-3

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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: C7H9BrClN
Molecular weight: 222.5

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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 chloride, 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：

  2,6-二甲基-2,5-环己二烯-1,4-二酮 、 2-溴-N-甲基苯胺盐酸盐 在 三乙胺 作用下， 以 异丙醇 为溶剂， 反应 2.0h， 以40%的产率得到2-(((2-bromophenyl)(methyl)amino)methyl)-6-methylbenzene-1,4-diol
  参考文献：
  名称：

  利用烷基醌互变异构：胺苯甲酰化

  摘要：

  据报道，通过烷基醌的侧链胺化合成苄基胺的一般方案。通过将烷基醌互变异构化为相应的醌甲基化物来引发反应，随后将其甲基化地被胺亲核试剂捕获。在温和条件下，质子溶剂中的叔胺促进了该过程，并且与许多官能团相容。1,2-和1,4-苯醌，以及萘醌，使用各种各样的伯胺和仲胺/苯胺参与该反应。还探讨了这种转化的综合效用。

  DOI：

  10.1021/acs.orglett.6b01629