3-羟基-1H-PHENALEN-1-酮 | 5472-84-4

• 分子结构分类: 有机化合物 - 苯类化合物 - 非那烯类
• 中文名称: 3-羟基-1H-PHENALEN-1-酮
• 中文别名: 3-羟基-1H-非那烯-1-酮
• 英文名称: 3-hydroxy-phenalen-1-one
• 英文别名: 3-hydroxy-1H-phenalen-1-one；3-hydroxyperinaphthenone；3-hydroxyphenalen-1-one
• CAS: 5472-84-4
• 化学式: C₁₃H₈O₂
• mdl: MFCD00029247
• 分子量: 196.205
• InChiKey: DXBYIIARRIMNFJ-UHFFFAOYSA-N

物化性质

• 熔点：
  264 °C(lit.)
• 沸点：
  293.09°C (rough estimate)
• 密度：
  1.1482 (rough estimate)
• 稳定性/保质期：
  避免与不相容的材料接触。与强氧化剂反应。

计算性质

• 辛醇/水分配系数(LogP)：
  2.5
• 重原子数：
  15
• 可旋转键数：
  0
• 环数：
  3.0
• 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

• 危险品标志：
  Xi
• 安全说明：
  S26,S36
• 危险类别码：
  R36/37/38
• 海关编码：
  2914400090
• 储存条件：
  密封保存，应储存在阴凉干燥的仓库中。

SDS

Name:	3-Hydroxy-1H-phenalen-1-one 98% Material Safety Data Sheet
Synonym:	None Known
CAS:	5472-84-4

Section 1 - Chemical Product MSDS Name:3-Hydroxy-1H-phenalen-1-one 98% Material Safety Data Sheet
Synonym:None Known

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Section 2 - COMPOSITION, INFORMATION ON INGREDIENTS

CAS#	Chemical Name	content	EINECS#
5472-84-4	3-Hydroxy-1H-phenalen-1-one	98%	unlisted

Hazard Symbols: XI
Risk Phrases: 36/37/38

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Section 3 - HAZARDS IDENTIFICATION
EMERGENCY OVERVIEW
Irritating to eyes, respiratory system and skin.
Potential Health Effects
Eye:
Causes eye irritation. May cause chemical conjunctivitis.
Skin:
Causes skin irritation.
Ingestion:
May cause irritation of the digestive tract. The toxicological properties of this substance have not been fully investigated.
Inhalation:
Causes respiratory tract irritation. The toxicological properties of this substance have not been fully investigated.
Chronic:
No information found.

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Section 4 - FIRST AID MEASURES
Eyes: Immediately flush eyes with plenty of water for at least 15 minutes, occasionally lifting the upper and lower eyelids. Get medical aid.
Skin:
Get medical aid. Flush skin with plenty of water for at least 15 minutes while removing contaminated clothing and shoes. Wash clothing before reuse.
Ingestion:
Never give anything by mouth to an unconscious person. Get medical aid. Do NOT induce vomiting. If conscious and alert, rinse mouth and drink 2-4 cupfuls of milk or water. Wash mouth out with water.
Inhalation:
Remove from exposure and move to fresh air immediately. If not breathing, give artificial respiration. If breathing is difficult, give oxygen. Get medical aid.
Notes to Physician:
Treat symptomatically and supportively.

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Section 5 - FIRE FIGHTING MEASURES
General Information:
As in any fire, wear a self-contained breathing apparatus in pressure-demand, MSHA/NIOSH (approved or equivalent), and full protective gear. During a fire, irritating and highly toxic gases may be generated by thermal decomposition or combustion.
Extinguishing Media:
Use water spray, dry chemical, carbon dioxide, or chemical foam.

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Section 6 - ACCIDENTAL RELEASE MEASURES
General Information: Use proper personal protective equipment as indicated in Section 8.
Spills/Leaks:
Vacuum or sweep up material and place into a suitable disposal container. Clean up spills immediately, observing precautions in the Protective Equipment section. Avoid generating dusty conditions.
Provide ventilation.

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Section 7 - HANDLING and STORAGE
Handling:
Minimize dust generation and accumulation. Avoid breathing dust, vapor, mist, or gas. Avoid contact with eyes, skin, and clothing.
Keep container tightly closed. Avoid ingestion and inhalation. Use with adequate ventilation. Wash clothing before reuse.
Storage:
Store in a cool, dry place. Store in a tightly closed container.

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Section 8 - EXPOSURE CONTROLS, PERSONAL PROTECTION
Engineering Controls:
Facilities storing or utilizing this material should be equipped with an eyewash facility and a safety shower. Use adequate ventilation to keep airborne concentrations low.
Exposure Limits CAS# 5472-84-4: Personal Protective Equipment Eyes: Wear appropriate protective eyeglasses or chemical safety goggles as described by OSHA's eye and face protection regulations in 29 CFR 1910.133 or European Standard EN166.
Skin:
Wear appropriate protective gloves to prevent skin exposure.
Clothing:
Wear appropriate protective clothing to prevent skin exposure.
Respirators:
Follow the OSHA respirator regulations found in 29 CFR 1910.134 or European Standard EN 149. Use a NIOSH/MSHA or European Standard EN 149 approved respirator if exposure limits are exceeded or if irritation or other symptoms are experienced.

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Section 9 - PHYSICAL AND CHEMICAL PROPERTIES

Physical State: Powder
Color: yellow - green
Odor: Not available.
pH: Not available.
Vapor Pressure: Not available.
Viscosity: Not available.
Boiling Point: Not available.
Freezing/Melting Point: 261-264 deg C
Autoignition Temperature: Not available.
Flash Point: Not available.
Explosion Limits, lower: Not available.
Explosion Limits, upper: Not available.
Decomposition Temperature:
Solubility in water:
Specific Gravity/Density:
Molecular Formula: C13H8O2
Molecular Weight: 196.21

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Section 10 - STABILITY AND REACTIVITY
Chemical Stability:
Not currently available.
Conditions to Avoid:
Dust generation.
Incompatibilities with Other Materials:
Strong oxidizing agents.
Hazardous Decomposition Products:
Carbon monoxide, carbon dioxide.
Hazardous Polymerization: Has not been reported

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Section 11 - TOXICOLOGICAL INFORMATION
RTECS#:
CAS# 5472-84-4 unlisted.
LD50/LC50:
Not available.
Carcinogenicity:
3-Hydroxy-1H-phenalen-1-one - Not listed by ACGIH, IARC, or NTP.

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Section 12 - ECOLOGICAL INFORMATION

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Section 13 - DISPOSAL CONSIDERATIONS
Dispose of in a manner consistent with federal, state, and local regulations.

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Section 14 - TRANSPORT INFORMATION

IATA
Shipping Name: Not regulated.
Hazard Class:
UN Number:
Packing Group:
IMO
Shipping Name: Not regulated.
Hazard Class:
UN Number:
Packing Group:
RID/ADR
Shipping Name: Not regulated.
Hazard Class:
UN Number:
Packing group:

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Section 15 - REGULATORY INFORMATION

European/International Regulations
European Labeling in Accordance with EC Directives
Hazard Symbols: XI
Risk Phrases:
R 36/37/38 Irritating to eyes, respiratory system
and skin.
Safety Phrases:
S 26 In case of contact with eyes, rinse immediately
with plenty of water and seek medical advice.
S 37/39 Wear suitable gloves and eye/face
protection.
WGK (Water Danger/Protection)
CAS# 5472-84-4: No information available.
Canada
None of the chemicals in this product are listed on the DSL/NDSL list.
CAS# 5472-84-4 is not listed on Canada's Ingredient Disclosure List.
US FEDERAL
TSCA
CAS# 5472-84-4 is not listed on the TSCA inventory.
It is for research and development use only.

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SECTION 16 - ADDITIONAL INFORMATION
N/A

反应信息

• 作为反应物：
  描述：

  3-羟基-1H-PHENALEN-1-酮 在 溴 、 溶剂黄146 作用下， 生成 2,2-dihydroxy-phenalene-1,3-dione
  参考文献：
  名称：

  Eistert,B. et al., Chemische Berichte, 1968, vol. 101, # 6, p. 2162 - 2175

  摘要：

  DOI：
• 作为产物：
  描述：

  3-aminophenalenone 在 氢氧化钾 作用下， 生成 3-羟基-1H-PHENALEN-1-酮
  参考文献：
  名称：

  Eistert,B. et al., Chemische Berichte, 1969, vol. 102, # 6, p. 1988 - 2002

  摘要：

  DOI：

文献信息

• Copper Ferrite Nanoparticles: An Efficient and Reusable Nanocatalyst for a Green One-Pot, Three-component Synthesis of Spirooxindoles in Water
  作者：Ayoob Bazgir、Ghaffar Hosseini、Ramin Ghahremanzadeh

  DOI：10.1021/co400057h

  日期：2013.10.14

  A green reaction of isatins, active cyanomethanes, and cyclic 1,3-dicarbonyl derivatives for the efficient and simple one-pot three-component synthesis of spirooxindole fused heterocycles in refluxing water by use of magnetically recoverable and reusable catalyst is reported. The features of this procedure are, the use of magnetically recoverable and reusable catalyst, mild reaction conditions, high

  据报道，通过使用可磁回收和可重复使用的催化剂，靛红，活性氰基甲烷和环状1,3-二羰基衍生物在回流水中进行高效，简单的一锅三组分合成螺环吲哚稠合杂环的绿色反应。该方法的特点是，使用可磁回收和可重复使用的催化剂，温和的反应条件，高至优异的产品收率，操作简便和后处理程序容易。最重要的是，催化剂容易的磁分离消除了反应完成后对催化剂过滤的需要。此外，即使重复使用5次，催化剂也保持高活性。
• One-Step Synthesis of Naphthofurandione, Benzofurandione, and Phenalenofuranone Derivatives by the CAN-Mediated Cycloaddition
  作者：Kazuhiro Kobayashi、Tomokazu Uneda、Koujirou Tanaka、Masako Mori、Hideo Tanaka、Osamu Morikawa、Hisatoshi Konishi

  DOI：10.1246/bcsj.71.1691

  日期：1998.7

  The 3+2-type cycloaddition reaction of 2-hydroxy-1,4-naphthoquinones with various alkenes or phenylacetylene was mediated by ammonium cerium(IV) nitrate (CAN) to give the corresponding naphtho[2,3-b]furan-4,9-dione and naphtho[1,2-b]furan-4,5-dione derivatives. The reaction of 2-hydroxy-1,4-benzoquinones with alkenes in the presence of CAN similarly proceeded to give benzofuran-4,7-dione and benzofuran-4,5-dione derivatives. 3-Hydroxy-1H-phenalen-1-one also underwent the CAN-mediated cycloaddition with alkenes or phenylacetylene to give the corresponding 7H-phenaleno[1,2-b]furan-7-one derivatives.

  2-羟基-1,4-萘醌与各种烯烃或苯乙炔在硝酸铈铵（CAN）的催化下发生3+2型环加成反应，生成相应的萘并[2,3-b]呋喃-4,9-二酮和萘并[1,2-b]呋喃-4,5-二酮衍生物。2-羟基-1,4-苯醌与烯烃在CAN存在下同样发生反应，得到苯并呋喃-4,7-二酮和苯并呋喃-4,5-二酮衍生物。3-羟基-1H-菲兰烯-1-酮也能在CAN的催化下与烯烃或苯乙炔发生环加成反应，生成相应的7H-菲兰诺[1,2-b]呋喃-7-酮衍生物。
• Efficient synthesis of phenalenone derivatives by rhodium(II)-catalyzed reactions
  作者：Yong Rok Lee、Jung Yup Suk

  DOI：10.1016/s0040-4039(00)00716-4

  日期：2000.6

  An efficient synthesis of phenalenone derivatives is achieved by rhodium(II)-catalyzed reactions of 2-diazo-1H-1,3-phenalenedione with a variety of substrates in moderate yields. This method also provides a rapid route to biologically interesting polycycles and heterocycles.

  通过铑（II）催化2-重氮1 H -1,3-苯二烯二酮与各种底物的铑（II）反应以中等收率实现了菲拉烯酮衍生物的有效合成。该方法还提供了快速的途径，可用于生物学上有趣的多环和杂环。
• Environmentally benign, one-pot synthesis of pyrans by domino Knoevenagel/6π-electrocyclization in water and application to natural products
  作者：Ene Jin Jung、Byung Ho Park、Yong Rok Lee

  DOI：10.1039/c0gc00265h

  日期：——

  In water medium, environmentally benign, facile, and efficient synthesis of pyrans was achieved in good yields by the reactions of a variety of cyclic 1,3-dicarbonyls with several α,β-unsaturated aldehydes. The key strategy was a formal [3+3] cycloaddition by domino Knoevenagel/6π- electrocyclization. This methodology was applied to the synthesis of biologically interesting pyranocoumarin, pyranoquinolinone, and pyranonaphthoquinone derivatives along with selected natural and non-natural products.

  在水相介质中，通过多种环状1,3-二羰基化合物与若干α,β-不饱和醛的反应，以良好产率实现了吡喃的环保、简便、高效合成。关键策略是形式上的[3+3]环加成，通过多米诺Knoevenagel缩合/6π电环化反应实现。这一方法被应用于生物活性吡喃香豆素、吡喃喹啉酮和吡喃萘醌衍生物的合成，以及部分天然与合成产物的制备。
• PHENALENE-1-ONE-CONTAINING PHOTOSENSITIZER COMPOSITION, PHENALENE-1-ONE COMPOUND AND THE USE THEREOF
  申请人：TriOptoTec GmbH

  公开号：US20200087259A1

  公开（公告）日：2020-03-19

  A phenalene-1-one compound, a photosensitizer composition including the phenalene-1-one compound, an article including the phenalene-1-one compound and/or photosensitizer composition and the use thereof.

  一种苯并吲哚酮化合物，一种包括该苯并吲哚酮化合物的光敏剂组合物，一种包括该苯并吲哚酮化合物和/或光敏剂组合物的物品以及其用途。

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