2-(4-羟基苯基)苯甲醛 | 400747-55-9

• 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-(4-羟基苯基)苯甲醛
• 中文别名: 4′-羟基联苯-2-甲醛
• 英文名称: 4'-hydroxy-[1,1'-biphenyl]-2-carbaldehyde
• 英文别名: 4'-Hydroxy-biphenyl-2-carbaldehyde；2-(4-hydroxyphenyl)benzaldehyde
• CAS: 400747-55-9
• 化学式: C₁₃H₁₀O₂
• mdl: MFCD04117373
• 分子量: 198.221
• InChiKey: PGLQTCNSJOJTIV-UHFFFAOYSA-N

物化性质

• 沸点：
  379.8±25.0 °C(Predicted)
• 密度：
  1.202±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  3
• 重原子数：
  15
• 可旋转键数：
  2
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  37.3
• 氢给体数：
  1
• 氢受体数：
  2

安全信息

• 海关编码：
  2912499000

SDS

Material Safety Data Sheet

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Section 1. Identification of the substance
Product Name: 4-(2-Formylphenyl)phenol
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: 4-(2-Formylphenyl)phenol
CAS number: 400747-55-9

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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: C13H10O2
Molecular weight: 198.2

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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.

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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-(4-羟基苯基)苯甲醛 在 silver orthophosphate 、 叠氮基三甲基硅烷 、 caesium carbonate 作用下， 以 乙醇 、 水 、 二甲基亚砜 为溶剂， 反应 18.0h， 生成
  参考文献：
  名称：

  银催化联苯乙炔的C≡C键加氢叠氮/自由基加成/环化反应：6-甲基磺酰化菲啶的一锅合成

  摘要：

  在温和的条件下描述了银催化的串联碳-碳三键加氢叠氮，自由基加成和联苯乙炔的环化，导致形成高产率的6-甲基磺酰化菲啶。在这种新颖的级联反应中，大多数原子都掺入了产物中，而没有裂解C bondC键。机理研究表明，该反应应通过亚氨基自由基反应性中间体进行。

  DOI：

  10.1021/acs.orglett.7b01771
• 作为产物：
  描述：

  2-甲酰基苯硼酸 、 alkaline earth salt of/the/ methylsulfuric acid 在 四(三苯基膦)钯 、 sodium carbonate 作用下， 以 乙醇 、 水 、 甲苯 为溶剂， 反应 24.0h， 以53%的产率得到2-(4-羟基苯基)苯甲醛
  参考文献：
  名称：

  使用2-苄基系留钌（II）/ TsDPEN络合物轴承η苯乙酮衍生物的不对称转移氢化6（ - p -OR）（R = H，我PR，BN，PH）的配体

  摘要：

  描述了一系列的4'-OR（R = H，iPr，Bn，Ph）取代的钌（II）联苯TsDPEN复合物；通过操作简单且可靠的两步配体合成，然后连接至钌（II）中心，即可获得络合物。我们报告了使用FA / TEA（5：2）作为还原剂，对这些新配合物的一系列主要苯乙酮衍生物的初步不对称转移氢化（ATH）结果；结果证实，这些催化剂能够在48小时内以优异的对映选择性还原底物。

  DOI：

  10.1016/j.jorganchem.2018.08.020

文献信息

• Palladium salt and functional reduced graphene oxide complex: in situ preparation of a generally applicable catalyst for C–C coupling reactions
  作者：Sheng Wang、Donghua Hu、Wenwen Hua、Jiangjiang Gu、Qiuhong Zhang、Xudong Jia、Kai Xi

  DOI：10.1039/c5ra10585d

  日期：——

  A novel Pd catalyst was designed by affording Pd2+ salt on the surface of functional reduced graphene oxide (FRGO), providing a new cheap and stable in situ prepared palladium catalyst for C–C coupling reactions, including the Heck reaction, Suzuki reaction, C–H bond functionalization reactions of thiophenes, and terminal alkyne C–H activation and homocoupling.

  一种新颖的钯催化剂是通过得到的Pd设计2+官能还原的石墨烯氧化物（FRGO）的表面上的盐，提供了一个新的廉价和稳定在原位对C-C偶联反应，包括Heck反应制备的钯催化剂，Suzuki反应，噻吩的C–H键官能化反应以及末端炔烃C–H活化和均偶联。
• Copper‐Catalyzed Chemo‐ and Diastereoselective 1,3‐Dipolar Cycloaddition of Carbonyl Ylide and Aldehyde‐Tethered‐Cyclohexadienone to Access Polycyclic Systems
  作者：Shiyong Peng、Hong Zhang、Yuqi Zhu、Ting Zhou、Jieyin He、Nuan Chen、Ming Lang、Hongguang Li、Jian Wang

  DOI：10.1002/adsc.202100648

  日期：2021.10.5

  A copper-catalyzed tandem intermolecular ylide formation/intramolecular cycloaddition of diazo compounds and aldehyde-tethered-cyclohexadienones was reported, chemo- and diastereoselectively providing oxapolycyclic frameworks in moderate to excellent yields under mild conditions. This reaction creates two C−C bonds and one C−O bond with five stereocentres including two all-carbon quaternary centres

  据报道，铜催化的重氮化合物和醛系环己二烯的串联分子间叶立德形成/分子内环加成，化学和非对映选择性地在温和条件下以中等至优异的产率提供氧多环骨架。该反应产生两个 C−C 键和一个 C−O 键，具有五个立体中心，包括两个全碳四元中心。此外，产品的后期多样化可以通过化学选择性取代来实现。
• COMPOUNDS OF PHOSPHINANES AND AZAPHOSPHINANES, A PROCESS FOR THEIR PREPARATION AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM
  申请人：LES LABORATOIRES SERVIER

  公开号：US20180016288A1

  公开（公告）日：2018-01-18

  Compounds of formula (I) wherein: Ak 1 represents an alkyl chain, X represents —(CH 2 ) m —, —CH(R)—, —N(R)—, —CH 2 —N(R)—, —N(R)—CH 2 — or —CH 2 —N(R)—CH 2 —, m and R are as defined in the description, R 1 and R 2 each represent H when X represents —(CH 2 ) m —, —CH(R)—, —N(R)—, —CH 2 —N(R)— or —N(R)—CH 2 —, or together form a bond when X represents —CH 2 —N(R)—CH 2 —, R 3 represents NH 2 , Cy-NH 2 , Cy-Ak 3 -NH 2 or piperidin-4-yl, Cy and Ak 3 are as defined in the description, R 4 and R 5 , which may be identical or different, each represent H or F, their optical isomers, and addition salts thereof with a pharmaceutically acceptable acid. Medicinal products containing the same which are useful in treating conditions requiring a TAFIa inhibitor.

  式(I)的化合物中： Ak1代表一个烷基链， X代表—(CH2)m—，—CH(R)—，—N(R)—，—CH2—N(R)—，—N(R)—CH2—或—CH2—N(R)—CH2—， m和R如描述中所定义， R1和R2分别在X代表—(CH2)m—，—CH(R)—，—N(R)—，—CH2—N(R)—或—N(R)—CH2—时代表H， 或者当X代表—CH2—N(R)—CH2—时，它们一起形成一个键， R3代表NH2，Cy-NH2，Cy-Ak3-NH2或哌啶-4-基， Cy和Ak3如描述中所定义， R4和R5，可能相同也可能不同，每个代表H或F， 它们的光学异构体， 以及它们与药学上可接受的酸形成的盐。 包含这些化合物的药品，在治疗需要TAFIa抑制剂的情况下有用。
• USE OF DICYCLOHEXYLMETHANOL DERIVATIVES HAVING ANTIMICROBIAL PROPERTIES
  申请人：MERCK PATENT GmbH

  公开号：US20150118172A1

  公开（公告）日：2015-04-30

  The present invention relates to the use of at least one dicyclohexylmethanol derivative of the formula (I) as antimicrobial active compound or as anti-acne, antidandruff, deodorant or antiperspirant active compound, to preparations comprising these compounds, and to specific dicyclohexylmethanol derivatives and to a process for the preparation thereof.

  本发明涉及将式(I)的至少一种二环己基甲醇衍生物用作抗微生物活性化合物或用作抗痘、抗头皮屑、除臭剂或止汗剂活性化合物，以及含有这些化合物的制剂，以及特定的二环己基甲醇衍生物及其制备方法。
• N-(Phenoxyalkyl) carboxamides and their use as antiarrhythmic agents
  申请人：American Cyanamid Company

  公开号：EP0792873A1

  公开（公告）日：1997-09-03

  The present invention relates to substituted ω-[phenoxy, phenylthio, phenylsulfinyl, phenylsulfonyl] [alkyl, alkenyl or alkynyl]amine carboxamides, sulfonamides and phosphonylamides which are useful as antiarrhythmic agents.

  本发明涉及替代的ω-[苯氧基、苯硫基、苯亚硫基、苯砜基][烷基、烯基或炔基]胺羧酰胺、磺胺和磷酰胺，其作为抗心律失常药物具有用途。