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反-4-氟肉桂醛 | 51791-26-5

中文名称
反-4-氟肉桂醛
中文别名
(E)-3-(4-氟苯基)-2-丙烯醛;对氟肉桂醛
英文名称
trans-4-fluorocinnamaldehyde
英文别名
4-fluorocinnamaldehyde;(E)-3-(4-fluorophenyl)acrylaldehyde;(E)-4-fluorocinnamaldehyde;p-fluorocinnamaldehyde;trans-p-fluorocinnamaldehyde;(2E)-3-(4-fluorophenyl)prop-2-enal;(E)-3-(4-fluorophenyl)acrolein;(E)-3-(4-fluorophenyl)prop-2-enal
反-4-氟肉桂醛化学式
CAS
51791-26-5;24654-55-5
化学式
C9H7FO
mdl
——
分子量
150.152
InChiKey
YSIYEWBILJZDQH-OWOJBTEDSA-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:
    24°C
  • 沸点:
    102-104°C
  • 密度:
    1.18

计算性质

  • 辛醇/水分配系数(LogP):
    1.9
  • 重原子数:
    11
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    17.1
  • 氢给体数:
    0
  • 氢受体数:
    2

安全信息

  • WGK Germany:
    3
  • 包装等级:
    III
  • 危险类别:
    8
  • 危险性防范说明:
    P280,P305+P351+P338
  • 危险品运输编号:
    1760
  • 危险性描述:
    H302,H318
  • 储存条件:
    存储条件:2~8°C,需密封。

SDS

SDS:c6bfdf737a2b224a3bc50a60b5fab9c1
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4-Fluorocinnamaldehyde Revision number: 5
SAFETY DATA SHEET

Section 1. IDENTIFICATION
Product name: 4-Fluorocinnamaldehyde

Revision number: 5

Section 2. HAZARDS IDENTIFICATION
GHS classification
PHYSICAL HAZARDS
Category 4
Flammable liquids
HEALTH HAZARDS
Category 2
Skin corrosion/irritation
Serious eye damage/eye irritation Category 2A
Not classified
ENVIRONMENTAL HAZARDS
GHS label elements, including precautionary statements
Pictograms or hazard symbols
Signal word Warning
Hazard statements Combustible liquid
Causes skin irritation
Causes serious eye irritation
Precautionary statements:
Keep away from flames and hot surfaces.
[Prevention]
Wash hands thoroughly after handling.
Wear protective gloves and eye/face protection.
[Response] IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses,
if present and easy to do. Continue rinsing.
If eye irritation persists: Get medical advice/attention.
IF ON SKIN: Gently wash with plenty of soap and water.
If skin irritation occurs: Get medical advice/attention.
Take off contaminated clothing and wash before reuse.
[Storage] Store in a well-ventilated place. Keep cool.
[Disposal] Dispose of contents/container through a waste management company authorized by
the local government.

Section 3. COMPOSITION/INFORMATION ON INGREDIENTS
Substance/mixture: Substance
Components: 4-Fluorocinnamaldehyde
Percent: >95.0%(GC)
24654-55-5
CAS Number:
Synonyms: 3-(4-Fluorophenyl)acrylaldehyde , 3-(4-Fluorophenyl)-2-propenal
4-Fluorocinnamaldehyde

Section 3. COMPOSITION/INFORMATION ON INGREDIENTS
Chemical Formula: C9H7FO

Section 4. FIRST AID MEASURES
Inhalation: Remove victim to fresh air and keep at rest in a position comfortable for breathing.
Get medical advice/attention if you feel unwell.
Skin contact: Remove/Take off immediately all contaminated clothing. Gently wash with plenty of
soap and water. If skin irritation or rash occurs: Get medical advice/attention.
Eye contact: Rinse cautiously with water for several minutes. Remove contact lenses, if present
and easy to do. Continue rinsing. If eye irritation persists: Get medical
advice/attention.
Get medical advice/attention if you feel unwell. Rinse mouth.
Ingestion:
Protection of first-aiders: A rescuer should wear personal protective equipment, such as rubber gloves and air-
tight goggles.

Section 5. FIRE-FIGHTING MEASURES
Dry chemical, foam, water spray, carbon dioxide.
Suitable extinguishing
media:
Unsuitable extinguishing Solid streams of water
media:
Specific hazards arising Take care as it may decompose upon combustion or in high temperatures to
from the chemical: generate poisonous fume.
Precautions for firefighters: Fire-extinguishing work is done from the windward and the suitable fire-extinguishing
method according to the surrounding situation is used. Uninvolved persons should
evacuate to a safe place. In case of fire in the surroundings: Remove movable
containers if safe to do so.
Special protective When extinguishing fire, be sure to wear personal protective equipment.
equipment for firefighters:

Section 6. ACCIDENTAL RELEASE MEASURES
Personal precautions, Use personal protective equipment. Keep people away from and upwind of spill/leak.
protective equipment and Ensure adequate ventilation. Entry to non-involved personnel should be controlled
emergency procedures: around the leakage area by roping off, etc.
Environmental precautions: Prevent product from entering drains.
Methods and materials for Absorb spilled material in a suitable absorbent (e.g. rag, dry sand, earth, saw-dust).
containment and cleaning In case of large amount of spillage, contain a spill by bunding. Adhered or collected
up: material should be promptly disposed of, in accordance with appropriate laws and
regulations.
Prevention of secondary Remove all sources of ignition. Fire-extinguishing devices should be prepared in
case of a fire. Use spark-proof tools and explosion-proof equipment.
hazards:

Section 7. HANDLING AND STORAGE
Precautions for safe handling
Technical measures: Handling is performed in a well ventilated place. Wear suitable protective equipment.
Prevent generation of vapour or mist. Keep away from flames and hot surfaces. Take
measures to prevent the build up of electrostatic charge. Use explosion-proof
equipment. Wash hands and face thoroughly after handling.
Use a closed system, ventilation.
Advice on safe handling: Avoid contact with skin, eyes and clothing.
Conditions for safe storage, including any
incompatibilities
Storage conditions: Keep container tightly closed. Store in a cool, dark and well-ventilated place.
Store under inert gas.
Store away from incompatible materials such as oxidizing agents.
Air-sensitive
Packaging material: Comply with laws.
4-Fluorocinnamaldehyde

Section 8. EXPOSURE CONTROLS / PERSONAL PROTECTION
Engineering controls: Install a closed system or local exhaust as possible so that workers should not be
exposed directly. Also install safety shower and eye bath.
Personal protective equipment
Respiratory protection: Vapor respirator. Follow local and national regulations.
Hand protection: Protective gloves.
Safety glasses. A face-shield, if the situation requires.
Eye protection:
Skin and body protection: Protective clothing. Protective boots, if the situation requires.

Section 9. PHYSICAL AND CHEMICAL PROPERTIES
Physical state (20°C): Liquid
Clear
Form:
Colour: Slightly pale yellow - Yellow
No data available
Odour:
pH: No data available
Melting point/freezing point:No data available
Boiling point/range: 95°C/0.3kPa
Flash point: No data available
Flammability or explosive
limits:
Lower: No data available
Upper: No data available
Relative density: 1.16
Solubility(ies):
[Water] No data available
No data available
[Other solvents]

Section 10. STABILITY AND REACTIVITY
Chemical stability: Stable under proper conditions.
Possibility of hazardous No special reactivity has been reported.
reactions:
Conditions to avoid: Open flame
Incompatible materials: Oxidizing agents
Hazardous decomposition Carbon monoxide, Carbon dioxide, Hydrogen fluoride
products:

Section 11. TOXICOLOGICAL INFORMATION
Acute Toxicity: No data available
Skin corrosion/irritation: No data available
Serious eye No data available
damage/irritation:
Germ cell mutagenicity: No data available
Carcinogenicity:
IARC = No data available
No data available
NTP =
Reproductive toxicity: No data available

Section 12. ECOLOGICAL INFORMATION
Ecotoxicity:
Fish: No data available
Crustacea: No data available
Algae: No data available
Persistence / degradability: No data available
No data available
Bioaccumulative
potential(BCF):
Mobility in soil
Log Pow: No data available
4-Fluorocinnamaldehyde

Section 12. ECOLOGICAL INFORMATION
Soil adsorption (Koc): No data available
Henry's Law No data available
constant(PaM3/mol):

Section 13. DISPOSAL CONSIDERATIONS
Recycle to process, if possible. Consult your local regional authorities. You may be able to burn in a chemical
incinerator equipped with an afterburner and scrubber system. Observe all federal, state and local regulations when
disposing of the substance.

Section 14. TRANSPORT INFORMATION
Does not correspond to the classification standard of the United Nations
Hazards Class:
UN-No: Not listed

Section 15. REGULATORY INFORMATION
Safe management ordinance of dangerous chemical product (State Council announces on January 26, 2002
and revised on February 16,2011): Safe use and production, the storage of a dangerous chemical, transport,
loading and unloading were prescribed.


SECTION 16 - ADDITIONAL INFORMATION
N/A

制备方法与用途

用途:用于有机合成及作为医药中间体。

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
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反应信息

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文献信息

  • Chiral Pincer Carbodicarbene Ligands for Enantioselective Rhodium-Catalyzed Hydroarylation of Terminal and Internal 1,3-Dienes with Indoles
    作者:Justin S. Marcum、Courtney C. Roberts、Rajith S. Manan、Tia N. Cervarich、Simon J. Meek
    DOI:10.1021/jacs.7b08575
    日期:2017.11.8
    Catalytic enantioselective addition of N-heteroarenes to terminal and internal 1,3-dienes is reported. Reactions are promoted by 5 mol % of Rh catalyst supported by a new chiral pincer carbodicarbene ligand that delivers allylic substituted arenes in up to 95% yield and up to 98:2 er. Mechanistic and X-ray evidence is presented that supports that the reaction proceeds via a Rh(III)-η3-allyl.
    据报道N-杂芳烃向末端和内部1,3-二烯的催化对映选择性加成。5 mol%的Rh催化剂促进了反应,该催化剂由新型手性钳碳二碳烯配体支撑,该配体可提供高达95%的收率和高达98:2 er的烯丙基取代的芳烃。机械和透视证据呈现支持经由铑(III)-η反应进行3 -烯丙基。
  • Metal- and Acid-Free Methyl Triflate Catalyzed Meyer–Schuster Rearrangement
    作者:Qingle Zeng、Lu Yang
    DOI:10.1055/s-0036-1588800
    日期:2017.7
    acid-free preparation of synthetically useful α,β-unsaturated carbonyl compounds from propargyl alcohols has been realized. This Meyer–Schuster rearrangement process is effectively catalyzed by methyl triflate (20 mol%) to prepare a broad scope of conjugated E-enals and E-enones generally in good to excellent yields (up to 90%). This reaction procedure operates under mild conditions (70 °C), in air
    摘要 已经实现了从炔丙醇中无金属和无酸地合成有用的α,β-不饱和羰基化合物的新方法。这种Meyer-Schuster重排过程可通过三氟甲磺酸甲酯(20摩尔%)有效催化,制备出大范围的共轭E-烯醛和E-烯酮,收率通常高达90%。该反应过程在温和条件下(70°C)在空气中进行,反应时间短(1 h)。此外,在该转化过程中分离出了被溶剂2,2,2-三氟乙醇捕获的碳正离子中间体。 已经实现了从炔丙醇中无金属和无酸地合成有用的α,β-不饱和羰基化合物的新方法。这种Meyer-Schuster重排过程可通过三氟甲磺酸甲酯(20摩尔%)有效催化,制备出大范围的共轭E-烯醛和E-烯酮,收率通常高达90%。该反应过程在温和条件下(70°C)在空气中进行,反应时间短(1 h)。此外,在该转化过程中分离出了被溶剂2,2,2-三氟乙醇捕获的碳正离子中间体。
  • Nickel-catalyzed allyl–allyl coupling reactions between 1,3-dienes and allylboronates
    作者:Ding-Wei Ji、Gu-Cheng He、Wei-Song Zhang、Chao-Yang Zhao、Yan-Cheng Hu、Qing-An Chen
    DOI:10.1039/d0cc02697b
    日期:——
    A regiospecific allyl–allyl coupling reaction between 1,3-dienes and allylboronates has been demonstrated under nickel catalysis. Salient features of this method include the earth-abundant metal catalyst, excellent regioselectivity and good functional group tolerance. Notably, even congested allyl substrates can also be applied to this protocol, thus allowing for the rapid preparation of a series of
    在镍催化下,已经证明了1,3-二烯和烯丙基硼酸酯之间的区域特异性烯丙基-烯丙基偶联反应。该方法的显着特征包括富含稀土的金属催化剂,优异的区域选择性和良好的官能团耐受性。值得注意的是,即使拥挤的烯丙基底物也可以应用于该方案,因此可以快速制备一系列有价值的1,5-二烯。
  • Sulfur-controlled and rhodium-catalyzed formal (3 + 3) transannulation of thioacyl carbenes with alk-2-enals and mechanistic insights
    作者:Qiuyue Wu、Ziyang Dong、Jiaxi Xu、Zhanhui Yang
    DOI:10.1039/d1ob00116g
    日期:——

    A rhodium-catalyzed denitrogenative formal (3 + 3) transannulation of 1,2,3-thiadiazoles with alk-2-enals is achieved and a mechanistic investigation is performed, with an inverse KIE of 0.49 obtained.

    通过铑催化的1,2,3-噻二唑与烯醛的脱氮形式(3 + 3)跨环反应已实现,并进行了机理研究,获得了0.49的逆动力学同位素效应。
  • [EN] NOVEL SESQUITERPENOID STAT3 INHIBITORS<br/>[FR] NOUVEAUX INHIBITEURS DE STAT3 SESQUITERPÉNOÏDES
    申请人:UNIV HAWAII
    公开号:WO2014205416A1
    公开(公告)日:2014-12-24
    The present disclosure provides a method of purifying pharmaceutical compositions consisting essentially of STAT3 inhibitors from a mixture of compounds, pharmaceutical compositions comprising STAT3 inhibitors used to inhibit STAT3 in tumor cells, and certain pharmaceutically acceptable salts thereof, and methods of use. The present disclosure features, in some embodiments, novel, potent and selective STAT3 inhibitors, including sesquiterpene lactone inhibitors.
    本公开提供了一种从化合物混合物中纯化主要由STAT3抑制剂组成的药物组合物的方法,所述药物组合物包括用于抑制肿瘤细胞中的STAT3的STAT3抑制剂,以及其某些药用可接受的盐,以及使用方法。本公开在某些实施例中具有新颖、强效和选择性的STAT3抑制剂,包括倍半萜内酯抑制剂。
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