2-溴-5-甲基磺酰硝基苯 | 94832-06-1

• 物质功能分类: 化学试剂 - 有机试剂
• 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-甲基磺酰硝基苯
• 中文别名: 2-溴-5-甲基磺酰基硝基苯
• 英文名称: 1-bromo-4-(methylsulfonyl)-2-nitrobenzene
• 英文别名: 2-Bromo-5-methylsulfonylnitrobenzene；1-bromo-4-methylsulfonyl-2-nitrobenzene
• CAS: 94832-06-1
• 化学式: C₇H₆BrNO₄S
• 分子量: 280.099
• InChiKey: ZRANEAXTVRBKGK-UHFFFAOYSA-N

物化性质

• 熔点：
  114-117

计算性质

• 辛醇/水分配系数(LogP)：
  1.7
• 重原子数：
  14
• 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：
  88.3
• 氢给体数：
  0
• 氢受体数：
  4

安全信息

• 危险品标志：
  Xi
• 包装等级：
  III
• 危险类别：
  6.1
• 危险性防范说明：
  P261,P264,P270,P271,P280,P302+P352,P304+P340,P310,P330,P361,P403+P233,P405,P501
• 危险品运输编号：
  2811
• 危险性描述：
  H301,H311,H331

SDS

Material Safety Data Sheet

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Section 1. Identification of the substance
Product Name: 2-Bromo-5-methylsulfonylnitrobenzene
Synonyms: 1-Bromo-4-methylsulfonyl-2-nitrobenzene

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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-5-methylsulfonylnitrobenzene
CAS number: 94832-06-1

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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: C7H6BrNO4S
Molecular weight: 280.1

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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, hydrogen bromide, sulfur 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：

  2-溴-5-甲基磺酰硝基苯 在 1,1'-双(二苯基膦)二茂铁 、 potassium phosphate 、 palladium diacetate 、 tin(ll) chloride 作用下， 以 四氢呋喃 、 N,N-二甲基乙酰胺 、 水 为溶剂， 生成 3-methyl-6-(methylsulfonyl)-1H-indol-1-ol
  参考文献：
  名称：

  通过 N-烯氧基吲哚的 [3,3]-Sigmatropic 重排简明合成呋喃 [2,3-b] 吲哚啉

  摘要：

  利用 N-链烯氧基吲哚中间体的反应性，开发了一种简洁的呋喃 [2,3-b] 吲哚啉合成路线。这些化合物自发地经历 [3,3]-σ 重排，然后环化形成作为单一非对映异构体的半缩氨酸。锡促进的 N-羟基吲哚形成，然后与活化炔烃的共轭加成提供了对各种 N-烯氧基吲哚及其相应呋喃 [2,3-b] 吲哚啉的简单和模块化的访问。微型高通量实验用于促进对这种转化的范围和耐受性的研究，并且还评估了对 N-羟基吲哚与卤代芳烃的亲核芳香取代和重排的相关研究。

  DOI：

  10.1055/s-0040-1707250
• 作为产物：
  描述：

  4-溴苯甲砜 在 硫酸 、 硝酸 作用下， 反应 0.5h， 以90.5%的产率得到2-溴-5-甲基磺酰硝基苯
  参考文献：
  名称：

  一种甲基磺草酮中间体的制备方法

  摘要：

  本发明涉及一种甲基磺草酮中间体的制备方法，对甲磺酰基溴苯作为起始原料，首先和硝酸发生硝化反应，将反应后体系用乙酸乙酯与饱和碳酸氢钠水溶液进行萃取处理，出去有机相得到产物；然后以DMF作为溶剂与氰化亚铜在高温下发生氰化反应，除去体系中溶剂，通过柱层析分离产物；将产物进行水解酸化得到最终产物甲基磺草酮中间体2‑硝基‑4‑（甲基磺酰基）苯甲酸。将该方法相比于传统的合成方法，减少了强氧化剂的使用，反应条件较为温和，增加了操作安全性，同时各步反应处理容易，有利于反应的进行，具有较高的产率。

  公开号：

  CN109134321A

文献信息

• [EN] PHENOXY ACETIC ACID DERIVATIVES<br/>[FR] DÉRIVÉS D'ACIDE PHÉNOXYACÉTIQUE
  申请人：MERCK SERONO SA

  公开号：WO2010092043A1

  公开（公告）日：2010-08-19

  The present invention provides phenoxyacetic acid derivatives of Formula (I) for the treatment of CRTH2 related disorders and disease selected from asthma, atopic dermatitis and inflammatory dermatoses.

  本发明提供了用于治疗与CRTH2相关的疾病和疾病（包括哮喘、特应性皮炎和炎症性皮肤病）的Formula（I）的苯氧乙酸衍生物。
• BROMODOMAIN INHIBITORS
  申请人：Quanticel Pharmaceuticals

  公开号：US20150111885A1

  公开（公告）日：2015-04-23

  The present invention relates to substituted heterocyclic derivative compounds, compositions comprising said compounds, and the use of said compounds and compositions for epigenetic regulation by inhibition of bromodomain-mediated recognition of acetyl lysine regions of proteins, such as histones. Said compositions and methods are useful for the treatment of cancer and neoplastic disease.

  本发明涉及替代杂环衍生物化合物，包括所述化合物的组合物，以及通过抑制溴结构域介导的蛋白质乙酰赖氨酸区域的识别来进行表观遗传调控的所述化合物和组合物的用途。所述组合物和方法对于癌症和肿瘤性疾病的治疗是有用的。
• Organocatalytic Enantioselective Direct Additions of Aldehydes to 4-Vinylpyridines and Electron-Deficient Vinylarenes and Their Synthetic Applications
  作者：Sinan Wang、Xiangmin Li、Hongwei Liu、Li Xu、Jinchen Zhuang、Jian Li、Hao Li、Wei Wang

  DOI：10.1021/ja511143b

  日期：2015.2.18

  We describe a synergistic catalysis strategy for the asymmetric direct addition of simple aldehydes to 4-vinylpyridines. By means of independent activation of weakly electrophilic 4-vinylpyridines by the Brønsted acid CF3SO3H (TfOH) and aldehydes by chiral diphenylprolinol tert-butyldimethylsilyl (TBDMS) ether-catalyzed formation of nucleophilic enamines in a cooperative manner, the previously unattainable

  我们描述了一种将简单醛不对称直接加成到 4-乙烯基吡啶的协同催化策略。通过 Brønsted 酸 CF3SO3H (TfOH) 独立激活弱亲电 4-乙烯基吡啶和手性二苯基脯氨醇叔丁基二甲基甲硅烷基 (TBDMS) 醚催化形成亲核烯胺，以协同方式形成以前无法实现的高度对映选择性加成过程第一次实现。值得注意的是，加成过程的强大之处在于其在生产具有合成价值的手性吡啶方面的高效率。(1) 该过程的 H NMR 研究表明，由手性胺催化剂和醛原位形成的亲核烯胺作为由 4-乙烯基吡啶生成的高活性亲电子试剂直接加到三聚 4-乙烯基吡啶鎓衍生物种中。 TfOH 的存在。此外，受吡啶和硝基苯类似电子性质的启发，我们实现了前所未有的手性二苯基脯氨醇 TBDMS 醚促进的、高度对映选择性的醛直接加成到 2-硝基苯乙烯，而无需使用 TfOH 作为助催化剂。在这种方法中，在 2-硝基苯乙烯上引入强吸电子基团，如 NO2、CF3、SO2Me
• Homogenous suspension of immunopotentiating compounds and uses thereof
  申请人：Skibinski David

  公开号：US09408907B2

  公开（公告）日：2016-08-09

  The present invention generally relates to homogeneous suspensions of small molecule immune potentiators (SMIPs) that are capable of stimulating or modulating an immune response in a subject in need thereof. The homogeneous suspensions may be used in combinations with various antigens or adjuvants for vaccine therapies.

  本发明通常涉及能够刺激或调节受需要者免疫反应的小分子免疫增强剂（SMIPs）的均匀悬浮液。这些均匀悬浮液可以与各种抗原或佐剂结合在一起用于疫苗治疗。
• [EN] COMPOUNDS AND COMPOSITIONS AS TLR ACTIVITY MODULATORS<br/>[FR] COMPOSÉS ET COMPOSITIONS SERVANT DE MODULATEURS DE L'ACTIVITÉ DES TLR
  申请人：IRM LLC

  公开号：WO2009111337A1

  公开（公告）日：2009-09-11

  The invention provides a novel class of compounds, pharmaceutical compositions comprising such compounds and methods of using such compounds to treat or prevent diseases or disorders associated with Toll-Like Receptors, including TLR7 and TLR8. In one aspect, the compounds are useful as adjuvants for enhancing the effectiveness of a vaccine (formula I) wherein: X3 is N; X4 is N Or CR3; X5 is -CR4=CR5.

  该发明提供了一类新型化合物，包括这些化合物的药物组合物以及使用这些化合物来治疗或预防与Toll样受体相关的疾病或紊乱的方法，包括TLR7和TLR8。在一个方面，这些化合物可用作辅助剂，以增强疫苗的效果（公式I），其中：X3为N；X4为N或CR3；X5为-CR4=CR5。