(乙氧基羰基甲基)三苯基氯化膦 | 17577-28-5

• 物质功能分类: 化学试剂 - 有机试剂 - 卤化磷
• 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: (乙氧基羰基甲基)三苯基氯化膦
• 中文别名: (羰基乙氧基甲基)三苯基氯化膦水合物
• 英文名称: (ethoxycarbonylmethyl)triphenylphosphonium chloride
• 英文别名: (carbethoxymethyl)triphenylphosphonium chloride；triphenyl carbethoxymethyl phosphonium chloride；(2-ethoxy-2-oxoethyl)triphenylphosphonium chloride；(2-ethoxy-2-oxoethyl)-triphenylphosphanium;chloride
• CAS: 17577-28-5
• 化学式: C₂₂H₂₂O₂P*Cl
• 分子量: 384.842
• InChiKey: DJGHVEPNEJKZBF-UHFFFAOYSA-M

物化性质

• 熔点：
  120-123 °C (dec.) 120-123 °C (lit.)
• 稳定性/保质期：
  常温常压下稳定，应避免接触氧化物。

计算性质

• 辛醇/水分配系数(LogP)：
  0.55
• 重原子数：
  26
• 可旋转键数：
  7
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.14
• 拓扑面积：
  26.3
• 氢给体数：
  0
• 氢受体数：
  3

安全信息

• TSCA：
  Yes
• 危险品标志：
  Xi
• 安全说明：
  S26,S36
• 危险类别码：
  R36/37/38
• WGK Germany：
  3
• 海关编码：
  2931900090
• 危险品运输编号：
  NONH for all modes of transport
• 危险标志：
  GHS07
• 危险性描述：
  H315,H319,H335
• 危险性防范说明：
  P261,P305 + P351 + P338
• 储存条件：
  常温下应密闭避光保存，并置于通风干燥处。

SDS

Name:	(Carboethoxymethyl)Triphenylphosphonium Chloride Hydrate 97% Material Safety Data Sheet
Synonym:	(4-Ethoxycarbonyl)Triphenylphosphonium Chloride
CAS:	17577-28-5

Section 1 - Chemical Product MSDS Name:(Carboethoxymethyl)Triphenylphosphonium Chloride Hydrate 97% Material Safety Data Sheet
Synonym:(4-Ethoxycarbonyl)Triphenylphosphonium Chloride

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Section 2 - COMPOSITION, INFORMATION ON INGREDIENTS

CAS#	Chemical Name	content	EINECS#
17577-28-5	(Carboethoxymethyl)Triphenylphosphoniu	97%	241-548-2

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.Hygroscopic (absorbs moisture from the air).
Potential Health Effects
Eye:
Causes eye irritation. May cause chemical conjunctivitis.
Skin:
Causes skin irritation.
Ingestion:
May cause gastrointestinal irritation with nausea, vomiting and diarrhea. 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. Can produce delayed pulmonary edema.
Chronic:
Effects may be delayed.

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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. Do NOT use mouth-to-mouth resuscitation.
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 tightly closed container. Keep refrigerated. (Store below 4C/39F.) Store protected from moisture. Store under nitrogen.

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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# 17577-28-5: 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: Solid
Color: white
Odor: Not available.
pH: Not available.
Vapor Pressure: Not available.
Viscosity: Not available.
Boiling Point: Not available.
Freezing/Melting Point: 121 deg C (Dec)
Autoignition Temperature: Not available.
Flash Point: Not available.
Explosion Limits, lower: Not available.
Explosion Limits, upper: Not available.
Decomposition Temperature: 121 deg C
Solubility in water:
Specific Gravity/Density:
Molecular Formula: C22H22ClO2P.xH2O
Molecular Weight: 384.58

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Section 10 - STABILITY AND REACTIVITY
Chemical Stability:
Stable at room temperature in closed containers under normal storage and handling conditions. Hygroscopic: absorbs moisture or water from the air.
Conditions to Avoid:
Incompatible materials, dust generation, exposure to air, excess heat, exposure to moist air or water.
Incompatibilities with Other Materials:
Moisture, oxidizing agents.
Hazardous Decomposition Products:
Hydrogen chloride, carbon monoxide, carbon dioxide, thermal decomposition may produce toxic fumes of phosphorous oxides and/or phosphine.
Hazardous Polymerization: Has not been reported

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Section 11 - TOXICOLOGICAL INFORMATION
RTECS#:
CAS# 17577-28-5 unlisted.
LD50/LC50:
Not available.
Carcinogenicity:
(Carboethoxymethyl)Triphenylphosphonium Chloride Hydrate - 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
Not regulated as a hazardous material.
IMO
Not regulated as a hazardous material.
RID/ADR
Not regulated as a hazardous material.

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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# 17577-28-5: No information available.
Canada
CAS# 17577-28-5 is listed on Canada's NDSL List.
CAS# 17577-28-5 is not listed on Canada's Ingredient Disclosure List.
US FEDERAL
TSCA
CAS# 17577-28-5 is listed on the TSCA inventory.

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SECTION 16 - ADDITIONAL INFORMATION
N/A

反应信息

• 作为反应物：
  描述：

  (乙氧基羰基甲基)三苯基氯化膦 在 RuCl2(1,3-dimesityl-imidazolidin-2-yl)(PCy3)(=CHPh) 、 potassium carbonate 、 potassium iodide 、 potassium hydroxide 作用下， 以 乙醇 、 二氯甲烷 、 乙二醇 、 丙酮 为溶剂， 反应 36.5h， 生成 蛇床子提取物
  参考文献：
  名称：

  Synthesis and anthelmintic activity of osthol analogs against Dactylogyrus intermedius in goldfish

  摘要：

  In an attempt to develop novel anthelmintic agents, our previously isolated osthol was used as lead structures for further optimization. In our research, a series of coumarin analogs, prepared from 7-hydroxy coumarin or 7-hydroxy-4-methyl coumarin, have been evaluated for their anthelmintic activities. In all of the compounds, 6 and 7 were first synthesized, and their structures were identified based on NMR and MS values. Among the candidates, 8-allyl-7-allyloxycoumarin showed better anthelmintic activity than other compounds against Dactylogyrus infestation with EC50 value of 1.81 mg/L The quantitative structure-activity relationship (QSAR) of 16 osthol analogs with anthelmintic activity expressed as pEC(50) and toxicity to goldfish expressed pLC(50), such results can offer useful theoretical references for future experimental works. (C) 2012 Elsevier Masson SAS. All rights reserved.

  DOI：

  10.1016/j.ejmech.2012.06.009
• 作为产物：
  描述：

  氯乙酸乙酯 、 三苯基膦 以81.9%的产率得到(乙氧基羰基甲基)三苯基氯化膦
  参考文献：
  名称：

  磷内鎓盐乙氧基碳乙氧基亚甲基三苯基磷烷的卤化汞（II）配合物的合成和结构表征

  摘要：

  已研究了叶立德乙氧基甲氧基亚甲基三苯基磷烷（EPPY）Ph 3 PCHCOOEt与卤化汞（II）的反应。所得的二聚汞（II）-内酯复合物为同构结构，形式为[（EPPY）（HgX 2）] 2，其中X为溴（1），氯（2）或碘（3）。这些配合物已通过光谱技术和X射线衍射进行了表征。业已表明，叶立德配体与汞（II）原子C配位。

  DOI：

  10.1016/j.jorganchem.2006.11.002
• 作为试剂：
  描述：

  青蒿素 在 Amberlyst A-21 、 (乙氧基羰基甲基)三苯基氯化膦 作用下， 以 四氢呋喃 为溶剂， 反应 0.03h， 以42%的产率得到artemisinin G
  参考文献：
  名称：

  Kalita, Biswajit; Barua, Nabin C.; Bez, Ghanashyam, Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry, 2003, vol. 42, # 10, p. 2622 - 2624

  摘要：

  DOI：

文献信息

• Substituted Disulfonamide Compounds
  申请人：REICH Melanie

  公开号：US20100152158A1

  公开（公告）日：2010-06-17

  Substituted disulfonamide compounds corresponding to formula I: In which R 1 , R 2 , R 3 , R 4a , R 4b , R 5a , R 5b , R 8 , R 9a , R 9b , R 10 , R 11 , a, b, s, t and A have defined meanings, pharmaceutical compositions containing one or more such compounds, processes for preparing such compounds, and a method of using such compounds for the treatment or inhibition of pain and/or other conditions mediated by the bradykinin receptor 1 (BR1).

  将对应于公式I的取代二磺酰胺化合物： 其中R 1 ，R 2 ，R 3 ，R 4a ，R 4b ，R 5a ，R 5b ，R 8 ，R 9a ，R 9b ，R 10 ，R 11 ，a，b，s，t和A具有定义的含义，包含一种或多种此类化合物的药物组合物，制备这种化合物的方法，以及使用这种化合物治疗或抑制由激肽酶受体1（BR1）介导的疼痛和/或其他病症的方法。
• One-Pot Synthesis of α,β-Unsaturated Esters, Ketones, and Nitriles from Alcohols and Phosphonium Salts
  作者：Xiaochun Yu、Shun Wang、Weijie Ding、Juan Hu、Huile Jin

  DOI：10.1055/s-0036-1590904

  日期：2018.1

  reacted not only with benzylic and heteroaromatic alcohols, but also with aliphatic alcohols, forming the corresponding α,β-unsaturated esters, ketones, and nitriles in moderate to excellent yields. A general method for the synthesis of α,β-unsaturated esters, ketones, and nitriles is successfully achieved by a one-pot copper-catalyzed oxidation with O2 in air as oxidant. The solvent mixture of acetonitrile

  摘要 通过在空气中以O 2为氧化剂的一锅铜催化氧化成功地实现了合成α，β-不饱和酯，酮和腈的通用方法。乙腈和甲酰胺（1：1）的溶剂混合物经过优化，可确保在一锅中有效地进行醇类的氧化，de盐的去质子化和Wittig反应。已针对该方法探索了广泛的底物，包括三个吸电子基团（CO 2 Et，COPh，CN）官能化的salts盐。它们不仅与苄基和杂芳族醇反应，而且与脂族醇反应，以中等至极好的收率形成相应的α，β-不饱和酯，酮和腈。 通过在空气中以O 2为氧化剂的一锅铜催化氧化成功地实现了合成α，β-不饱和酯，酮和腈的通用方法。乙腈和甲酰胺（1：1）的溶剂混合物经过优化，可确保在一锅中有效地进行醇类的氧化，de盐的去质子化和Wittig反应。已针对该方法探索了广泛的底物，包括三个吸电子基团（CO 2 Et，COPh，CN）官能化的salts盐。它们不仅与苄基和杂芳族醇反应，而且与脂族醇反应，以中等至极
• One-pot synthesis of 2,4,5-trisubstituted oxazoles from N-acyl amino acids by a combination of cyclodehydration with N,N′-diisopropylcarbodiimide and Wittig olefination
  作者：Wenhua Huang、Guangping Dong、Zumureti Mijiti

  DOI：10.1016/j.tet.2011.12.004

  日期：2012.1

  By a combination of cyclodehydration of N-acyl amino acids with N,N′-diisopropylcarbodiimide (DIC) and non-classical Wittig olefination of the resultant 5(4H)-oxazolones with Ph3PCHCN and Ph3PCHCOOEt, 5-oxazoleacetonitriles and 5-oxazoleacetates were synthesized in one-pot in 41–85% and 57–70% yields, respectively.

  通过环化脱水的的组合ñ -酰基氨基酸与Ñ，Ñ '-diisopropylcarbodiimide（DIC）和所得到的5（4的非经典Wittig烯ħ）-oxazolones的Ph 3 P CHCN且Ph 3 P CHCOOEt，5-一锅合成恶唑乙腈和5-恶唑乙酸盐，产率分别为41-85％和57-70％。
• Direct Wittig Olefination of Alcohols
  作者：Qiang-Qiang Li、Zaher Shah、Jian-Ping Qu、Yan-Biao Kang

  DOI：10.1021/acs.joc.7b02720

  日期：2018.1.5

  A base-promoted transition metal-free approach to substituted alkenes using alcohols under aerobic conditions using air as the inexpensive and clean oxidant is described. Aldehydes are relatively difficult to handle compared to corresponding alcohols due to their volatility and penchant to polymerize and autoxidize. Wittig ylides are easily oxidized to aldehydes and consequently form homo-olefination

  描述了在有氧条件下使用醇作为廉价且清洁的氧化剂，使用醇在碱性条件下使用无醇过渡醇取代烯烃的方法。与相应的醇相比，由于醛的挥发性和聚合和自氧化倾向，因此醛相对较难处理。维蒂希酸根易于氧化成醛，因此形成均烯烃化产物。首次通过同时原位生成乙叉和乙叉的策略，无需预先制备醛或乙叉醇就将醇直接转移到烯烃中。因此，实现了二醇的二/单可控烯烃化。这种合成实用的方法已用于克级合成的药物，如DMU-212和白藜芦醇。
• Aryltriolborates as Air- and Water-Stable Bases for Wittig Olefination
  作者：Wenhua Huang、Shuang-Hong Zhao、Ning Xu

  DOI：10.1055/s-0034-1378919

  日期：——

  1-tris(hydroxymethyl)ethane, and aqueous tetrabutylammonium hydroxide. The aryltriolborates can be used as bases in Wittig reactions of aromatic aldehydes with all three types of phosphorus ylides: stabilized and semistabilized ylides can be generated at room temperature, and nonstabilized ylides at 120 °C (bath temperature). Tetrabutylammonium aryltriolborates have been synthesized in 37–66% yield by a one-pot

  摘要 通过一锅法从芳基硼酸，1,1,1-三（羟甲基）乙烷和四丁基氢氧化铵水溶液一锅法合成了芳基三硼酸四丁基铵硼酸酯。三芳基硼酸酯可以用作芳族醛与所有三种类型的磷酰化物的Wittig反应的碱：可以在室温下生成稳定和半稳定的化物，并在120°C（浴温）下生成不稳定的化物。 通过一锅法从芳基硼酸，1,1,1-三（羟甲基）乙烷和四丁基氢氧化铵水溶液一锅法合成了芳基三硼酸四丁基铵硼酸酯。三芳基硼酸酯可以用作芳族醛与所有三种类型的磷酰化物的Wittig反应的碱：可以在室温下生成稳定和半稳定的化物，并在120°C（浴温）下生成不稳定的化物。