3-溴-4-硝基苯甲醚 | 98447-30-4

• 物质功能分类: 有机原料 - 醚类化合物及其衍生物
• 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: 3-溴-4-硝基苯甲醚
• 英文名称: 2-bromo-4-methoxy-1-nitrobenzene
• 英文别名: 3-bromo-4-nitroanisole
• CAS: 98447-30-4
• 化学式: C₇H₆BrNO₃
• mdl: MFCD06797977
• 分子量: 232.034
• InChiKey: RYKPDLZQIABTMY-UHFFFAOYSA-N

物化性质

• 熔点：
  69℃

计算性质

• 辛醇/水分配系数(LogP)：
  2.5
• 重原子数：
  12
• 可旋转键数：
  1
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.142
• 拓扑面积：
  55
• 氢给体数：
  0
• 氢受体数：
  3

安全信息

• 海关编码：
  2909309090
• 危险性防范说明：
  P280,P305+P351+P338
• 危险性描述：
  H302
• 储存条件：
  室温且干燥

SDS

Material Safety Data Sheet

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Section 1. Identification of the substance
Product Name: 2-Bromo-4-methoxy-1-nitrobenzene
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-methoxy-1-nitrobenzene
CAS number: 98447-30-4

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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: C7H6BrNO3
Molecular weight: 232.0

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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.

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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：

  3-溴-4-硝基苯甲醚 在 偶氮二异丁腈 吡啶 、 盐酸 、 三正丁基氢锡 、 铁粉 、 sodium hydride 作用下， 以 四氢呋喃 、 乙醚 、 乙醇 、 甲苯 为溶剂， 反应 0.5h， 生成 1,3-二甲基-5-甲氧基吲哚啉-2-酮
  参考文献：
  名称：

  正式的合成染料木素

  摘要：

  近来已用于生物碱黄雀碱的全合成中的关键羟吲哚中间体（2）是通过利用自由基环化的短而有效的途径制备的。

  DOI：

  10.1016/s0040-4039(01)91381-4
• 作为产物：
  描述：

  5-甲氧基-2-硝基苯甲酸 在 氧气 、 silver carbonate 、 potassium hydroxide 、 copper(ll) bromide 作用下， 以 二甲基亚砜 、 N,N-二甲基甲酰胺 为溶剂， 以25%的产率得到3-溴-4-硝基苯甲醚
  参考文献：
  名称：

  银催化的羧酸脱羧卤化

  摘要：

  报道了由碳酸银催化的羧酸的脱羧卤化。在130-140°C下，邻硝基硝基苯甲酸与氯化铜（II）或溴化物在DMF / DMSO中反应，以中等至良好的产率生成相应的芳基卤化物。

  DOI：

  10.1016/j.tetlet.2010.10.054

文献信息

• Substituted dibenzo[ c,h ]cinnolines: topoisomerase I-targeting anticancer agents
  作者：Younong Yu、Sudhir K Singh、Angela Liu、Tsai-Kun Li、Leroy F Liu、Edmond J LaVoie

  DOI：10.1016/s0968-0896(02)00604-1

  日期：2003.4

  9-methylenedioxybenzo[i]phenanthridine is one of the more potent benzo[i]phenanthridine derivatives in regard to topoisomerase I-targeting activity and cytotoxicity. The structure-activity relationship observed with these substituted dibenzo[c,h]cinnolines parallels that observed for benzo[i]phenanthridine derivatives. Compared to similarly substituted benzo[i]phenanthridines, the dibenzo[c,h]cinnoline analogues

  合成了几种取代的二苯并[c，h]肉桂啉，并评估了其靶向拓扑异构酶I的潜力以及相对的细胞毒性活性。选择的苯并[i]菲啶能够稳定由拓扑异构酶I和DNA形成的可裂解复合物。开始这项研究以检查本质上是苯并[i]菲啶的氮杂类似物的二苯并[c，h] cinnolines是否具有相似的药理特性。就靶向拓扑异构酶I的活性和细胞毒性而言，2，3-二甲氧基-8，9-亚甲基二氧基苯并[i]菲啶是更有效的苯并[i]菲啶衍生物之一。用这些取代的二苯并[c，h] cinnolines观察到的结构活性关系与苯并[i]菲啶衍生物观察到的相似。与类似取代的苯并[i]菲啶相比，二苯并[c，h] cinnoline类似物表现出更强的拓扑异构酶I靶向活性和细胞毒性。在评估2,3-二甲氧基-8,9-亚甲基二氧基二苯并[c，h] cinnoline和2,3-二甲氧基-8,9-亚甲基二氧基苯并[i]菲啶在人淋巴母细胞瘤中的细胞毒性时获
• Sparing the ortho-position in nucleophilic aromatic substitution-specific displacement of the 4-SePh group in 2,4-bis(phenylseleno)nitrobenzene
  作者：Nicolai Stuhr-Hansen、Thorstein Finn Götze、Lars Henriksen、Theis Ivan Sølling、Annette Langkilde、Henning Osholm Sørensen

  DOI：10.1002/hc.20519

  日期：——

  Upon treatment of o- and p-(phenylseleno)nitrobenzenes with sodium methoxide quantitative exchange reactions took place, affording the corresponding methoxynitrobenzenes. Upon reaction between 2,4-bis(phenylseleno)nitrobenzene 2 and sodium methoxide, an unusual regiopure formation of 4-methoxy-2-(phenylseleno)nitrobenzene 3 was observed. This product remained unreactive toward an excess of sodium methoxide

  用甲醇钠处理邻和对（苯基硒基）硝基苯后发生定量交换反应，得到相应的甲氧基硝基苯。在 2,4-双（苯基硒基）硝基苯 2 和甲醇钠反应后，观察到 4-甲氧基-2-（苯基硒基）硝基苯 3 的异常区域纯形成。该产品对过量的甲醇钠保持不反应，从而阻止了 2,4-二甲氧基硝基苯 6 的形成。通过合成研究、X 射线晶体学和 DFT 计算检查了反应物和中间体 Meisenheimer 配合物的性质。我们发现观察到的选择性可以根据传统的共振考虑来理解。© 2009 Wiley Periodicals, Inc. 杂原子化学 20:101–108, 2009; 在线发表于 Wiley InterScience (www. interscience.wiley.com）。DOI 10.1002/hc.20519
• [EN] BICYCLIC HETEROARYL SUBSTITUTED COMPOUNDS<br/>[FR] COMPOSÉS BICYCLIQUES SUBSTITUÉS PAR HÉTÉROARYLE
  申请人：BRISTOL MYERS SQUIBB CO

  公开号：WO2018013774A1

  公开（公告）日：2018-01-18

  Disclosed are compounds of Formula (I) to (VIII): (I) (II) (III) (IV) (V) (VI) (VII) (VIII); or a stereoisomer, tautomer, pharmaceutically acceptable salt, solvate or prodrug thereof, wherein R3 is a bicyclic heteroaryl group substituted with zero to 3 R3a; and R1, R2, R3a, R4, and n are defined herein. Also disclosed are methods of using such compounds as PAR4 inhibitors, and pharmaceutical compositions comprising such compounds. These compounds are useful in inhibiting or preventing platelet aggregation, and are useful for the treatment of a thromboembolic disorder or the primary prophylaxis of a thromboembolic disorder.

  公开了公式(I)至(VIII)的化合物：(I) (II) (III) (IV) (V) (VI) (VII) (VIII)；或其立体异构体、互变异构体、药物可接受的盐、溶剂化物或前药，其中R3是与0至3个R3a取代的双环杂芳基团；且R1、R2、R3a、R4和n在此定义。还公开了使用这些化合物作为PAR4抑制剂的方法，以及包含这些化合物的药物组合物。这些化合物用于抑制或预防血小板聚集，用于治疗血栓栓塞障碍或作为血栓栓塞障碍的初级预防。
• [EN] IMIDAZO [4, 5 -C] PYRIDINE DERIVATIVES USEFUL FOR THE TREATMENT OF DEGENERATIVE AND INFLAMMATORY DISEASES<br/>[FR] DÉRIVÉS D'IMIDAZO[4, 5-C]PYRIDINES UTILES POUR LE TRAITEMENT DE MALADIES DÉGÉNÉRATIVES ET INFLAMMATOIRES
  申请人：GALAPAGOS NV

  公开号：WO2013117645A1

  公开（公告）日：2013-08-15

  Wherein R1, L1, R3, R4, Cy, L2 and R5 are as defined herein. Novel imidazolopyridines according to Formula I, able to inhibit JAK are disclosed, these compounds may be prepared as a pharmaceutical composition, and may be used for the prevention and treatment of a variety of conditions in mammals including humans, including by way of non-limiting example, allergic or inflammatory conditions, autoimmune diseases, proliferative diseases, transplantation rejection, diseases involving impairment of cartilage turnover, congenital cartilage malformations, and/or diseases associated with hypersecretion of IL6 or interferons.

  在此，R1、L1、R3、R4、Cy、L2和R5的定义如下。根据公式I披露了新型咪唑吡啶类化合物，能够抑制JAK，这些化合物可以制备为药物组合物，并可用于预防和治疗包括人类在内的哺乳动物的各种疾病，例如过敏性或炎症性疾病、自身免疫疾病、增生性疾病、移植排斥、涉及软骨周转障碍的疾病、先天软骨畸形以及与IL6或干扰素过度分泌相关的疾病。
• Nitration of deactivated aromatic compounds via mechanochemical reaction
  作者：Jian-Wei Wu、Pu Zhang、Zhi-Xin Guo

  DOI：10.1016/j.tetlet.2021.153087

  日期：2021.5

  A variety of deactivated arenes were nitrated to their corresponding nitro derivatives in excellent yields under high-speed ball milling condition using Fe(NO3)3·9H2O/P2O5 as nitrating reagent. A radical involved mechanism was proposed for this facial, eco-friendly, safe, and effective nitration reaction.

  使用Fe（NO 3）3 ·9H 2 O / P 2 O 5作为硝化剂，在高速球磨条件下，各种失活的芳烃都以极高的收率被硝化为相应的硝基衍生物。针对这种面部，生态友好，安全和有效的硝化反应，提出了一种涉及自由基的机制。