2-硝基-4-(苯基甲氧基)-苯酚 | 96315-18-3

• 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-硝基-4-(苯基甲氧基)-苯酚
• 英文名称: 4-(benzyloxy)-2-nitrophenol
• 英文别名: 2-nitro-4-phenylmethoxy-phenol；2-nitro-4-phenylmethoxyphenol
• CAS: 96315-18-3
• 化学式: C₁₃H₁₁NO₄
• 分子量: 245.235
• InChiKey: VRYYLYCOPKQGPS-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.5
• 重原子数：
  18
• 可旋转键数：
  3
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.08
• 拓扑面积：
  75.3
• 氢给体数：
  1
• 氢受体数：
  4

安全信息

• 海关编码：
  2909500000

SDS

Material Safety Data Sheet

---

Section 1. Identification of the substance
Product Name: 4-(Benzyloxy)-2-nitrophenol
Synonyms:

---

Section 2. Hazards identification
Harmful by inhalation, in contact with skin, and if swallowed.

---

Section 3. Composition/information on ingredients.
Ingredient name: 4-(Benzyloxy)-2-nitrophenol
CAS number: 96315-18-3

---

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.

---

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.

---

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.

---

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:

---

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.

---

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: C13H11NO4
Molecular weight: 245.2

---

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.

---

Section 11. Toxicological information
No data.

---

Section 12. Ecological information
No data.

---

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.

---

Section 14. Transportation information
Non-harzardous for air and ground transportation.

---

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.

---

SECTION 16 - ADDITIONAL INFORMATION
N/A

制备方法与用途

4-苯氧基-2-硝基苯酚是一种可用于合成荧光离子指示剂的重要中间体。

反应信息

• 作为反应物：
  描述：

  2-硝基-4-(苯基甲氧基)-苯酚 在 溶剂黄146 、 锌 作用下， 以 乙醇 为溶剂， 反应 25.0h， 生成 5-benzyloxy-3H-benzooxazole-2-thione
  参考文献：
  名称：

  设计，合成和药理的主动脉选择性酰基辅酶A：胆固醇O酰基转移酶（ACAT / SOAT）抑制剂

  摘要：

  我们描述了我们的主动脉选择性酰基辅酶A：胆固醇O-酰基转移酶（ACAT，也缩写为SOAT）抑制剂的分子设计，其结构-活性关系（SARs）以及它们的药代动力学（PK）和药理学特征。两个弱配体-N-（2,6-二异丙基苯基）乙酰胺（50％抑制浓度[IC 50 ] = 8.6μM）和2-（甲硫基）苯并[ d ]恶唑（IC 50  = 31μM）的连接包括6支亚甲基链的连接体，得到一种高度有效分子，9-（苯并[ d ]恶唑-2-基硫基） - ñ - （2,6-二异丙基）壬酰胺（3H），其表现出高效力（IC 50 = 0.004μM）朝向主动脉ACAT。这种从头到尾的设计使将活性显着提高到2150至7750倍，并基于双重诱导的拟合机制来区分同工型选择性成为可能。在1 mg / kg和3 mg / kg的剂量下，3h显着降低了主动脉弓的脂质蓄积面积，分别降至74％和69％，而没有降低高脂和高胆固醇喂养的F

  DOI：

  10.1016/j.bmc.2018.06.024
• 作为产物：
  描述：

  4-苄氧基苯酚 在 aluminum(III) nitrate nonahydrate 、 硫酸 、 silica gel 作用下， 以 二氯甲烷 为溶剂， 反应 3.25h， 以75%的产率得到2-硝基-4-(苯基甲氧基)-苯酚
  参考文献：
  名称：

  Aluminum nitrate and silica sulfuric acid as efficient nitrating media for the mononitration of phenols under mild and heterogeneous conditions

  摘要：

  室温下，在湿二氧化硅（50% w/w）存在下，在二氯甲烷中将 Al(NO3)3-9H2O 与二氧化硅硫酸结合，成功地硝化了多种苯酚衍生物，并获得了中等至良好的产率。

  DOI：

  10.1139/v09-081

文献信息

• A Synthetic Fluorescent Mitochondria‐Targeted Sensor for Ratiometric Imaging of Calcium in Live Cells
  作者：Diana Pendin、Rosa Norante、Andrea De Nadai、Gaia Gherardi、Nicola Vajente、Emy Basso、Nina Kaludercic、Cristina Mammucari、Cristina Paradisi、Tullio Pozzan、Andrea Mattarei

  DOI：10.1002/anie.201902272

  日期：2019.7.15

  Ca2+ handling by mitochondria is crucial for cell life and the direct measure of mitochondrial Ca2+ concentration in living cells is of pivotal interest. Genetically‐encoded indicators greatly facilitated this task, however they require demanding delivery procedures. On the other hand, existing mitochondria‐targeted synthetic Ca2+ indicators are plagued by several drawbacks, for example, non‐specific

  线粒体对Ca 2+的处理对于细胞生命至关重要，直接测量活细胞中线粒体Ca 2+的浓度至关重要。基因编码的指标极大地促进了这一任务，但是它们要求苛刻的交付程序。另一方面，现有的以线粒体为靶标的合成Ca 2+指示剂受到若干缺点的困扰，例如非特异性定位，泄漏，毒性。在这里，我们报告了一种新型的荧光Ca 2+传感器mt-fura-2的合成和表征，该传感器是通过将两个三苯基phosph阳离子与Ca 2+指示剂fura-2的分子骨架偶联而获得的。Mt-fura-2结合Ca 2+用的≈1.5μ的解离常数米体外。当以乙酰氧基甲基酯的形式负载在不同的细胞类型中时，该探针显示出适当的线粒体定位并可以准确测量基质[Ca 2+ ]的变化，证明其优于现有染料。我们描述了mt-fura-2的合成，表征以及将其应用于遗传编码指示剂难以递送的细胞类型。
• Intracellular click reaction with a fluorescent chemical Ca2+ indicator to prolong its cytosolic retention
  作者：Yoshiaki Takei、Atsushi Murata、Kento Yamagishi、Satoshi Arai、Hideki Nakamura、Takafumi Inoue、Shinji Takeoka

  DOI：10.1039/c3cc42489h

  日期：——

  The powerful strategy of “intracellular click reaction” was used to retain a chemical Ca2+ indicator in the cytosol. Specifically, a novel clickable Ca2+ indicator “N3-fura-2 AM” was coupled with dibenzylcyclooctyl-modified biomacromolecules via copper-free click reaction in living cells and Ca2+ oscillation was observed for an extended period of time.

  利用“细胞内点击反应”的强大策略，将一种化学钙离子指示剂保留在细胞质中。具体而言，一种新型的可点击钙离子指示剂“N3-fura-2 AM”通过无铜点击反应与双苄基环辛基修饰的生物大分子结合于活细胞内，并观测到长时间的钙离子振荡。
• A Mild Procedure for the Preparation of o-Nitrophenols by Nitro Urea or Ammonium Nitrate in the Presence of Silica Sulfuric Acid (SiO2-OSO3H)
  作者：Arash Ghorbani-Choghamarani、Mohsen Nikoorazm、Hamid Goudarziafshar、Zahra Naserifar、Parisa Zamani

  DOI：10.1002/cjoc.201190148

  日期：2011.4

  A mixture of ammonium nitrate or nitro urea and silica sulfuric acid was found to be efficient and environmentally friendly nitrating media for the preparation of orto‐nitro phenols in dichloromethane at room temperature.

  发现硝酸铵或硝基尿素与二氧化硅硫酸的混合物是在室温下在二氯甲烷中制备邻硝基硝基苯酚的高效和环境友好型硝化介质。
• Anilide compounds and drugs containing the same
  申请人：Kowa Company, Ltd.

  公开号：US06362208B1

  公开（公告）日：2002-03-26

  The invention relates to a novel anilide compound and a pharmaceutical composition comprising the same. The invention relates to a compound represented by the following general formula: represents a divalent residue of benzene with a substituent(s), heterocycle-condensed benzene which may or may not have a substituent, pyridine which may or may not have a substituent, cyclohexane or naphthalene or Ar represents an aryl group which may or may not have a substituent; X represents —NH—, oxygen atom or sulfur atom; Y represents —NR4—, oxygen atom, sulfur atom, sulfoxide or sulfone; Z represents single bond or —NR5—; R4 represents hydrogen atom, a lower alkyl group, an aryl group or a silylated lower alkyl group which may or may not have a substituent; R5 represents hydrogen atom, a lower alkyl group, an aryl group or a silylated lower alkyl group which may or may not have a substituent; and n represents an integer of 0 to 15. The inventive compounds are useful in the form of pharmaceutical composition, specifically as acyl coenzyme A cholesterol acyltransferase (ACAT) inhibitor.

  该发明涉及一种新型苯胺类化合物和包含该化合物的药物组合物。该发明涉及一种由以下通用式表示的化合物：表示苯的一个带有取代基的二价残基，杂环并联苯可能具有或不具有取代基，吡啶可能具有或不具有取代基，环己烷或萘或Ar代表可能具有或不具有取代基的芳基；X代表—NH—、氧原子或硫原子；Y代表—NR4—、氧原子、硫原子、亚硫醚或砜；Z代表单键或—NR5—；R4代表氢原子、较低烷基、芳基或可能具有或不具有取代基的硅烷化较低烷基；R5代表氢原子、较低烷基、芳基或可能具有或不具有取代基的硅烷化较低烷基；n代表0到15之间的整数。这些创新化合物在药物组合物的形式中非常有用，特别作为酰辅酶A胆固醇酰转移酶（ACAT）抑制剂。
• Compound
  申请人：——

  公开号：US20040019016A1

  公开（公告）日：2004-01-29

  There is provided a compound of Formula I 1 wherein each T is independently selected from H, hydrocarbyl, —F—R, and a bond with one of D, E, P or Q, or together with one of P and Q forms a ring; Z is a suitable atom the valency of which is m; D, E and F are each independently of each other an optional linker group, wherein when Z is nitrogen E is other than CH 2 and C═O; P, Q and R are independently of each other a ring system; and at least Q comprises a sulphamate group.

  提供了一个式I1的化合物，其中每个T分别选自H、烃基、—F—R和与D、E、P或Q中的一个之一形成键，或者与P和Q中的一个一起形成环；Z是一个适当的原子，其价数为m；D、E和F分别独立于彼此，是可选的连接基团，其中当Z是氮时，E不是CH2和C═O；P、Q和R独立于彼此，是一个环系统；至少Q包含一个磺酰胺基团。