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methyl 4-(3-oxo-3-phenyl-1-propenyl)benzoate | 98258-72-1

中文名称
——
中文别名
——
英文名称
methyl 4-(3-oxo-3-phenyl-1-propenyl)benzoate
英文别名
Methyl-4-(3-oxo-3-phenylpropenyl)-benzoate;methyl 4-(3-oxo-3-phenylprop-1-enyl)benzoate
methyl 4-(3-oxo-3-phenyl-1-propenyl)benzoate化学式
CAS
98258-72-1
化学式
C17H14O3
mdl
——
分子量
266.296
InChiKey
CADDVOXTZYEXKQ-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

物化性质

  • 熔点:
    119-120 °C
  • 沸点:
    369.5°C (rough estimate)
  • 密度:
    1.1601 (rough estimate)
  • 稳定性/保质期:
    遵照规定使用和储存,则不会分解。

计算性质

  • 辛醇/水分配系数(LogP):
    2.9
  • 重原子数:
    20
  • 可旋转键数:
    5
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.06
  • 拓扑面积:
    43.4
  • 氢给体数:
    0
  • 氢受体数:
    3

安全信息

  • 危险品标志:
    Xi
  • 危险类别码:
    R36/37/38
  • 海关编码:
    2918300090
  • 安全说明:
    S26,S37/39
  • 储存条件:
    存储在阴凉干燥的地方。

SDS

SDS:948474f4c444e88f51115815d379ec4f
查看
Name: Methyl 4-(3-Oxo-3-Phenyl-1-Propenyl) Benzoate 98+% (NMR) Material Safety Data Sheet
Synonym: None Known
CAS: 98258-72-1
Section 1 - Chemical Product MSDS Name:Methyl 4-(3-Oxo-3-Phenyl-1-Propenyl) Benzoate 98+% (NMR) Material Safety Data Sheet
Synonym:None Known

Section 2 - COMPOSITION, INFORMATION ON INGREDIENTS
CAS# Chemical Name content EINECS#
98258-72-1 Methyl 4-(3-Oxo-3-Phenyl-1-Propenyl) B 98+% unlisted
Hazard Symbols: XI
Risk Phrases: 36/37/38

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 gastrointestinal irritation with nausea, vomiting and diarrhea.
Inhalation:
Causes respiratory tract irritation. Can produce delayed pulmonary edema.
Chronic:
Effects may be delayed.

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.
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.

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. Runoff from fire control or dilution water may cause pollution.
Extinguishing Media:
Use agent most appropriate to extinguish fire. Use water spray, dry chemical, carbon dioxide, or appropriate foam.

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.

Section 7 - HANDLING and STORAGE
Handling:
Wash thoroughly after handling. Remove contaminated clothing and wash before reuse. Minimize dust generation and accumulation. Avoid contact with eyes, skin, and clothing. Keep container tightly closed.
Avoid ingestion and inhalation. Use with adequate ventilation.
Storage:
Keep container closed when not in use. Store in a tightly closed container. Store in a cool, dry, well-ventilated area away from incompatible substances.

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 process enclosure, local exhaust ventilation, or other engineering controls to control airborne levels.
Exposure Limits CAS# 98258-72-1: 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:
A respiratory protection program that meets OSHA's 29 CFR 1910.134 and ANSI Z88.2 requirements or European Standard EN 149 must be followed whenever workplace conditions warrant respirator use.

Section 9 - PHYSICAL AND CHEMICAL PROPERTIES

Physical State: Solid
Color: yellow
Odor: Not available.
pH: Not available.
Vapor Pressure: Not available.
Viscosity: Not available.
Boiling Point: Not available.
Freezing/Melting Point: 119.00 - 120.00 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: negligible
Specific Gravity/Density:
Molecular Formula: C17H14O3
Molecular Weight: 266.29

Section 10 - STABILITY AND REACTIVITY
Chemical Stability:
Stable at room temperature in closed containers under normal storage and handling conditions.
Conditions to Avoid:
Incompatible materials, dust generation, excess heat, strong oxidants.
Incompatibilities with Other Materials:
Oxidizing agents.
Hazardous Decomposition Products:
Carbon monoxide, irritating and toxic fumes and gases, carbon dioxide.
Hazardous Polymerization: Has not been reported

Section 11 - TOXICOLOGICAL INFORMATION
RTECS#:
CAS# 98258-72-1 unlisted.
LD50/LC50:
Not available.
Carcinogenicity:
Methyl 4-(3-Oxo-3-Phenyl-1-Propenyl) Benzoate - Not listed by ACGIH, IARC, or NTP.

Section 12 - ECOLOGICAL INFORMATION


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

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:

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# 98258-72-1: No information available.
Canada
None of the chemicals in this product are listed on the DSL/NDSL list.
CAS# 98258-72-1 is not listed on Canada's Ingredient Disclosure List.
US FEDERAL
TSCA
CAS# 98258-72-1 is not listed on the TSCA inventory.
It is for research and development use only.


SECTION 16 - ADDITIONAL INFORMATION
N/A

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    methyl 4-(3-oxo-3-phenyl-1-propenyl)benzoate 在 hydrido(phosphonite)cobalt(I) 、 频那醇硼烷 作用下, 以 为溶剂, 反应 16.0h, 以84%的产率得到4-(3-氧代-3-苯基丙基)苯甲酸甲酯
    参考文献:
    名称:
    光控钴催化 α,β-不饱和酮的选择性硼氢化
    摘要:
    摘要亲核试剂与 α,β-不饱和羰基化合物的 1,2 和 1,4 加成之间的选择性通常通过向底物或试剂中添加化学计量添加剂来改变,以增加其“硬”或“软”特性。在这里,我们展示了一种概念上不同的方法,该方法依赖于用可见光控制催化剂的配位范围。通过这种方式,我们使反应偏向两条不同的途径,从而在 α,β-不饱和酮的催化硼氢化中产生对比产物。这包括通过 1,4-选择性硼氢化反应直接获得以前难以捉摸的环状烯醇硼酸盐,为一锅法获得稀有的顺醇醛产品提供了一种直接且立体选择性的途径。DFT 计算和机械实验证实了两种不同的机制是有效的,支撑着这种不寻常的光控选择性开关。
    DOI:
    10.1002/ange.202009893
  • 作为产物:
    描述:
    苯乙酮对甲酰基苯甲酸甲酯 在 sodium hydroxide 作用下, 以 乙醇 为溶剂, 反应 0.17h, 生成 methyl 4-(3-oxo-3-phenyl-1-propenyl)benzoate
    参考文献:
    名称:
    Rh(II)催化的硝基转移[5 +1]芳基取代的乙烯基环丙烷的环加成
    摘要:
    据报道,在芳基取代的乙烯基环丙烷和亚硝烯前体之间存在正式的[5 +1]环加成反应。该方法采用Rh 2(esp)2作为催化剂,导致取代的四氢吡啶的高度区域选择性的形成。初步的机理研究支持逐步的极性机制,这是由先前观察到的Rh-类肾上腺素的路易斯酸度引起的。总的来说,这项工作将六元环的形成扩展了氮杂环转移环加成反应的应用,后者是一种相对未开发的杂环合成方法。
    DOI:
    10.1021/acs.orglett.9b00594
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文献信息

  • Synthesis of dihydroquinolinones <i>via</i> iridium-catalyzed cascade C–H amidation and intramolecular aza-Michael addition
    作者:Changduo Pan、Zhenkun Yang、Hao Xiong、Jiangang Teng、Yun Wang、Jin-Tao Yu
    DOI:10.1039/c8cc09751h
    日期:——
    An iridium-catalyzed annulation of chalcones with sulfonyl azides via cascade C–H amidation and intramolecular aza-Michael addition was developed, affording a variety of 2-aryl-2,3-dihydro-4-quinolones in moderate to good yields. This reaction features easy operation, readily available starting materials, and the cascade formation of two C–N bonds in one pot.
    通过级联的C–H酰胺化和分子内的氮杂-Michael加成反应,开发了铱催化的磺酰叠氮化物对查尔酮的环化反应,提供了中等至良好收率的各种2-芳基-2,3-二氢-4-喹诺酮类化合物。该反应具有易于操作,易于获得的原料以及在一个反应​​釜中级联形成两个C–N键的特点。
  • 2,3-二氢喹啉-4-酮类化合物的制备方法
    申请人:江苏理工学院
    公开号:CN109535076B
    公开(公告)日:2021-09-28
    本发明属于医药化工技术领域,具体涉及一种2,3‑二氢喹啉‑4‑酮类化合物的制备方法,该方法以查尔酮类化合物及对甲苯磺酰叠氮为原料,经催化剂催化合成2,3‑二氢喹啉‑4‑酮类化合物。与以往的合成手段相比,该反应具有操作简便、原料易得、适用范围广等优点。
  • Inhibitors of histone deacetylase
    申请人:MethylGene, Inc.
    公开号:US06541661B1
    公开(公告)日:2003-04-01
    The invention relates to the inhibition of histone deacetylase. The invention provides compounds and methods for inhibiting histone deacetylase enzymatic activity. The invention also provides compositions and methods for treating cell proliferative diseases and conditions.
    这项发明涉及抑制组蛋白去乙酰化酶。该发明提供了抑制组蛋白去乙酰化酶酶活性的化合物和方法。该发明还提供了治疗细胞增殖性疾病和病况的组合物和方法。
  • Pd-Catalyzed Carbonylative Conjugate Addition of Dialkylzinc Reagents to Unsaturated Carbonyls
    作者:Daniel W. Custar、Hai Le、James P. Morken
    DOI:10.1021/ol1013476
    日期:2010.9.3
    The Pd-catalyzed addition of organozinc reagents to unsaturated carbonyls in the presence of carbon monoxide provides 1,4-diketones in good yield. The reaction was studied with a number of substituted cyclic and acyclic ketones as well as α,β-unsaturated aldehydes.
    在存在一氧化碳的情况下,Pd 催化的有机锌试剂与不饱和羰基化合物的加成以良好的产率提供了 1,4-二酮。用许多取代的环状和无环酮以及 α,β-不饱和醛研究了该反应。
  • Nickel-catalysed cyclopropanation of electron-deficient alkenes with diiodomethane and diethylzinc
    作者:Jin Xu、Nazurah Binte Samsuri、Hung A. Duong
    DOI:10.1039/c5cc10296k
    日期:——
    An inexpensive nickel catalyst enables cyclopropanation of electron-deficient olefins under modified Furukawa's procedure in moderate to good yields.
    廉价的镍催化剂可在改良的Furukawa程序下以中等至良好的收率对缺电子烯烃进行环丙烷化反应。
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