(S)-3-苯基环戊酮 | 86505-50-2

• 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: (S)-3-苯基环戊酮
• 英文名称: (S)-3-phenylcyclopentanone
• 英文别名: 3-phenylcyclopentanone；3-phenylcyclopentan-1-one；(S)-3-phenylcyclopentan-1-one；(3S)-3-phenylcyclopentanone；(3S)-3-phenylcyclopentan-1-one
• CAS: 86505-50-2
• 化学式: C₁₁H₁₂O
• 分子量: 160.216
• InChiKey: MFBXYJLOYZMFIN-JTQLQIEISA-N

物化性质

• 沸点：
  155 °C / 10mmHg

计算性质

• 辛醇/水分配系数(LogP)：
  1.8
• 重原子数：
  12
• 可旋转键数：
  1
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.36
• 拓扑面积：
  17.1
• 氢给体数：
  0
• 氢受体数：
  1

安全信息

• 海关编码：
  2914399090
• 储存条件：
  室温

SDS

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Section I.Chemical Product and Company Identification
Chemical Name (S)-3-Phenylcyclopentanone
Portland OR
Cyclopentanone, 3-phenyl- (3S)- (9 CI)
Synonym
C11H12O
Chemical Formula
CAS Number 86505-50-2

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Section II. Composition and Information on Ingredients
Chemical Name CAS Number Percent (%) TLV/PEL Toxicology Data
(S)-3-Phenylcyclopentanone 86505-50-2 Min. 98.0 Not available. Not available.
(GC)

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Section III. Hazards Identification
Acute Health Effects Irritating to eyes and skin on contact. Inhalation causes irritation of the lungs and respiratory system. Inflammation of the
eye is characterized by redness, watering, and itching. Skin inflammation is characterized by itching, scaling, reddening,
or, occasionally, blistering.
Follow safe industrial hygiene practices and always wear proper protective equipment when handling this compound.
CARCINOGENIC EFFECTS : Not available.
Chronic Health Effects
MUTAGENIC EFFECTS : Not available.
TERATOGENIC EFFECTS : Not available.
DEVELOPMENTAL TOXICITY: Not available.
Repeated or prolonged exposure to this compound is not known to aggravate existing medical conditions.

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Section IV. First Aid Measures
Eye Contact Check for and remove any contact lenses. In case of contact, immediately flush eyes with plenty of water for at least 15
minutes. Get medical attention.
Skin Contact In case of contact, immediately flush skin with plenty of water. Remove contaminated clothing and shoes. Wash clothing
before reuse. Thoroughly clean shoes before reuse. Get medical attention.
If the victim is not breathing, perform mouth-to-mouth resuscitation. Loosen tight clothing such as a collar, tie, belt or
Inhalation
waistband. If breathing is difficult, oxygen can be administered. Seek medical attention if respiration problems do not
improve.
Ingestion INDUCE VOMITING by sticking finger in throat. Lower the head so that the vomit will not reenter the mouth and throat.
Loosen tight clothing such as a collar, tie, belt or waistband. If the victim is not breathing, perform mouth-to-mouth
resuscitation. Examine the lips and mouth to ascertain whether the tissues are damaged, a possible indication that the
toxic material was ingested; the absence of such signs, however, is not conclusive.

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Section V. Fire and Explosion Data
Not available.
Auto-Ignition
Flammability May be combustible at high temperature.
Flash Points Flammable Limits Not available.
Not available.
Combustion Products These products are toxic carbon oxides (CO, CO2).
Fire Hazards
Not available.
Risks of explosion of the product in presence of mechanical impact: Not available.
Explosion Hazards
Risks of explosion of the product in presence of static discharge: Not available.
Fire Fighting Media SMALL FIRE: Use DRY chemical powder.
and Instructions LARGE FIRE: Use water spray, fog or foam. DO NOT use water jet.
Consult with local fire authorities before attempting large scale fire-fighting operations.
Continued on Next Page
(S)-3-Phenylcyclopentanone

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Section VI. Accidental Release Measures
Spill Cleanup Irritating material. Hygroscopic material.
Absorb with an inert material and put the spilled material in an appropriate waste disposal. Finish cleaning the spill by
Instructions
rinsing any contaminated surfaces with copious amounts of water. Consult federal, state, and/or local authorities for
assistance on disposal.

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Section VII. Handling and Storage
Handling and Storage IRRITANT. HYGROSCOPIC. Keep away from heat. Mechanical exhaust required. When not in use, tightly seal the
container and store in a dry, cool place. Avoid excessive heat and light. Do not breathe gas/fumes/ vapor/spray.
Information
Always store away from incompatible compounds such as oxidizing agents.

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Section VIII. Exposure Controls/Personal Protection
Engineering Controls Provide exhaust ventilation or other engineering controls to keep the airborne concentrations of vapors below their
respective threshold limit value. Ensure that eyewash station and safety shower is proximal to the work-station location.
Personal Protection Splash goggles. Lab coat. Vapor respirator. Boots. Gloves. Suggested protective clothing might not be sufficient;
consult a specialist BEFORE handling this product. Be sure to use a MSHA/NIOSH approved respirator or equivalent.
Exposure Limits Not available.

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Section IX. Physical and Chemical Properties
Solubility
Physical state @ 20°C Liquid. (Clear, colorless.) Not available.
Not available.
Specific Gravity
Molecular Weight 160.21 Partition Coefficient Not available.
Boiling Point 155°C (311°F) @ 10 mmHg Vapor Pressure Not available.
Melting Point Not available. Vapor Density Not available.
Not available. Volatility Not available.
Refractive Index
Critical Temperature Not available. Odor Not available.
Viscosity Not available. Taste Not available.

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Section X. Stability and Reactivity Data
Stability

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This material is stable if stored under proper conditions. (See Section VII for instructions)
Conditions of Instability Avoid excessive heat and light.
Incompatibilities
Reactive with oxidizing agents.

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Section XI. Toxicological Information
Not available.
RTECS Number
Eye Contact. Ingestion. Inhalation.
Routes of Exposure
Toxicity Data Not available.
Chronic Toxic Effects CARCINOGENIC EFFECTS : Not available.
MUTAGENIC EFFECTS : Not available.
TERATOGENIC EFFECTS : Not available.
DEVELOPMENTAL TOXICITY: Not available.
Repeated or prolonged exposure to this compound is not known to aggravate existing medical conditions.
Acute Toxic Effects Irritating to eyes and skin on contact. Inhalation causes irritation of the lungs and respiratory system. Inflammation of the
eye is characterized by redness, watering, and itching. Skin inflammation is characterized by itching, scaling, reddening,
or, occasionally, blistering.
Follow safe industrial hygiene practices and always wear proper protective equipment when handling this compound.
Continued on Next Page
(S)-3-Phenylcyclopentanone

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Section XII. Ecological Information
Ecotoxicity Not available.
Not available.
Environmental Fate

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Section XIII. Disposal Considerations
Recycle to process, if possible. Consult your local regional authorities. You may be able to dissolve or mix material with a
Waste Disposal
combustible solvent and burn in a chemical incinerator equipped with an afterburner and scrubber system. Observe all
federal, state and local regulations when disposing of the substance.

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Section XIV. Transport Information
DOT Classification Not a DOT controlled material (United States).
Not applicable.
PIN Number
Proper Shipping Name
Not applicable.
Packing Group (PG) Not applicable.
DOT Pictograms

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Section XV. Other Regulatory Information and Pictograms
TSCA Chemical Inventory This product is NOT on the EPA Toxic Substances Control Act (TSCA) inventory. The following notices are required by 40
CFR 720.36 (C) for those products not on the inventory list:
(EPA)
(i) These products are supplied solely for use in research and development by or under the supervision of a technically
qualified individual as defined in 40 CFR 720.0 et sec.
(ii) The health risks of these products have not been fully determined. Any information that is or becomes available will be
supplied on an MSDS sheet.
WHMIS Classification Not available.
(Canada)
EINECS Number (EEC) Not available.
EEC Risk Statements R36/37/38- Irritating to eyes, respiratory system and skin.

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SECTION 16 - ADDITIONAL INFORMATION
N/A

反应信息

• 作为反应物：
  描述：

  (S)-3-苯基环戊酮 在 盐酸羟胺 、 sodium acetate 作用下， 以 乙醇 、 水 为溶剂， 反应 2.5h， 生成 (S)-3-phenyl-cyclopentanone oxime
  参考文献：
  名称：

  [EN] COMPLEMENT PATHWAY MODULATORS AND USES THEREOF
  [FR] MODULATEURS DE LA VOIE DU COMPLÉMENT ET LEURS UTILISATIONS

  摘要：

  公开号：

  WO2014002051A3
• 作为产物：
  描述：

  [(1S,2R,4S)-1,7,7-trimethyl-2-bicyclo[2.2.1]heptanyl] 3-oxo-6-phenylhexanoate 在 甲醇 、 Rh₂(R)-(PTPA)4 、 三乙胺 、 甲烷磺酰基叠氮化物 作用下， 以 乙腈 为溶剂， 反应 6.0h， 生成 (S)-3-苯基环戊酮
  参考文献：
  名称：

  α-重氮β-酮酯分子内CH插入反应的双重不对称诱导

  摘要：

  摘要 通过使用四[N-邻苯二甲酰基-(R)或(S)-苯丙氨酸二铑]作为α-重氮β分子内CH插入的同手性催化剂，在CC键形成中实现了一种新的双不对称诱导。 -同手性醇的酮酯。(+)-新薄荷酯和衍生自(R)-苯丙氨酸的催化剂的匹配组合在去除酯基后产生高达80%ee的旋光3-取代环戊酮。

  DOI：

  10.1080/00397919408010251

文献信息

• Design and Synthesis of Polymeric Chiral Bicyclo[3.3.0] Diene as Reusable Ligand for Rhodium-Catalyzed Asymmetric 1,4-Addition
  作者：Hongyu Yang、Minghua Xu

  DOI：10.1002/cjoc.201201079

  日期：2013.1

  A series of A‐B type sterically regular bicyclio[3.3.0] diene‐based polymers were designed and synthesized as immobilized chiral diene ligands for asymmetric catalysis. With polymeric diene 6b, good to excellent enantioselectivities can be achieved in Rh‐catalyzed asymmetric 1,4‐addition of arylboronic acids to α,β‐unsaturated ketones.

  设计并合成了一系列基于A‐B型空间正则双环[3.3.0]二烯的聚合物，作为固定的手性二烯配体进行不对称催化。使用聚合二烯6b，可以在Rh催化的芳基硼酸的不对称1,4-加成反应中获得出色的对映选择性，对α，β-不饱和酮。
• Readily Accessible Chiral Diene Ligands for Rh-Catalyzed Enantioselective Conjugate Additions of Boronic Acids
  作者：Barry M. Trost、Aaron C. Burns、Thomas Tautz

  DOI：10.1021/ol201754c

  日期：2011.9.2

  the broad scope of the Pd-catalyzed asymmetric alkylation of meso- and d,l-divinylethylene carbonate, several chiral diene ligands were prepared in two steps from commercial materials. Subsequently, these ligands were evaluated in the Rh-catalyzed asymmetric conjugate addition of boronic acids to enones.

  由于Pd催化的内消旋和d，1-二乙烯基碳酸亚乙酯的不对称烷基化反应的广泛范围，从商业原料中分两步制备了几种手性二烯配体。随后，在硼酸到烯酮的Rh催化的不对称共轭加成中评估了这些配体。
• Chiral N-tert-butanesulfinyl α,β-unsaturated ketimine: a simple and highly effective olefin/sulfinimide hybrid ligand for asymmetric 1,4-additions
  作者：Xiangqing Feng、Beibei Wei、Jing Yang、Haifeng Du

  DOI：10.1039/c1ob05971h

  日期：——

  One novel type of chiral olefin/sulfinimide hybrid ligands has been developed through a simple one-step condensation of α,β-unsaturated ketones with tert-butanesulfinamide and utilized successfully for rhodium-catalyzed asymmetric conjugated additions to furnish the desired adducts in high yields with excellent ee's.

  通过α，β-不饱和酮与化合物的简单一步缩合，已经开发出一种新型的手性烯烃/亚磺酰亚胺杂化配体 叔丁烷亚磺酰胺 并成功地用于铑催化的不对称共轭加成中，从而以优异的ee高收率提供所需的加合物。
• Chiral Sulfoxide-Olefin Ligands: Completely Switchable Stereoselectivity in Rhodium-Catalyzed Asymmetric Conjugate Additions
  作者：Guihua Chen、Jiangyang Gui、Liangchun Li、Jian Liao

  DOI：10.1002/anie.201102586

  日期：2011.8.8

  it both ways: A novel class of chiral sulfoxide‐olefin ligands was synthesized from a single chiral source. These ligands were evaluated in rhodium‐catalyzed 1,4‐additions of arylboronic acids to electron‐deficient olefins, and remarkable olefin‐directed reversal of stereoselectivity (up to >99 % ee, R isomer; 98 % ee, S isomer) was observed when the reversal ligand pair L1 (branched olefin) and L2

  两者兼有：从单一手性来源合成了一类新型的手性亚砜-烯烃配体。在铑催化的芳基硼酸的1,4加成反应中，对这些配体进行了评估，并观察到电子不足的烯烃，并 观察到烯烃定向的立体选择性显着逆转（高达99％ee，R 异构体； 98％ee，S异构体）。当使用反向配体对L1（支链烯烃）和L2（直链烯烃）时（参见方案）。
• Highly Practical Catalytic Asymmetric 1,4-Addition of Arylboronic Acids in Water Using New Hydrophilic Chiral Bicyclo[3.3.0] Diene Ligands
  作者：Chen-Guo Feng、Zhi-Qian Wang、Cheng Shao、Ming-Hua Xu、Guo-Qiang Lin

  DOI：10.1021/ol801665z

  日期：2008.9.18

  The first Rh-diene-catalyzed aqueous asymmetric 1,4-addition of alpha,beta-unsaturated carbonyl compounds with arylboronic acids has been realized. By using a hydrophilic bicyclo[3.3.0] diene ligand, the reactions can be performed successfully in neat water at room temperature to afford the corresponding products in good yields and with very high enantioselectivities for both cyclic and linear substrates

  已经实现了第一Rh-二烯催化的α，β-不饱和羰基化合物与芳基硼酸的不对称1，4-加成水溶液。通过使用亲水性双环[3.3.0]二烯配体，可以在室温下于纯水中成功地进行反应，从而以高收率和对环和线性底物都具有非常高的对映选择性提供相应的产物。