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烯丙基-1,1,2,2-四氟乙基醚 | 1428-33-7

中文名称
烯丙基-1,1,2,2-四氟乙基醚
中文别名
四氟丙烯酸乙酯
英文名称
1,1,2,2-tetrafluoroethyl allyl ether
英文别名
2H-Perfluoroethyl allyl ether;allyl-(1,1,2,2-tetrafluoro-ethyl)-ether;Allyl-(1,1,2,2-tetrafluor-aethyl)-aether;1,1,2,2-tetrafluorethylpropen(2)-1-yl-ether;3-(1,1,2,2-tetrafluoroethoxy)propene;HCF2CF2OCH2CH=CH2;Allyl 1,1,2,2-tetrafluoroethyl ether;3-(1,1,2,2-tetrafluoroethoxy)prop-1-ene
烯丙基-1,1,2,2-四氟乙基醚化学式
CAS
1428-33-7
化学式
C5H6F4O
mdl
MFCD00043822
分子量
158.096
InChiKey
DTDFWYZVBJYVPL-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

  • 沸点:
    76-78°C
  • 密度:
    1,2 g/cm3
  • 闪点:
    -5°C
  • 大气OH速率常数:
    1.90e-11 cm3/molecule*sec

计算性质

  • 辛醇/水分配系数(LogP):
    2.3
  • 重原子数:
    10
  • 可旋转键数:
    4
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.6
  • 拓扑面积:
    9.2
  • 氢给体数:
    0
  • 氢受体数:
    5

安全信息

  • 危险等级:
    3.1
  • 危险品标志:
    F,Xn
  • 危险类别码:
    R20/22,R11
  • 危险品运输编号:
    UN 3271
  • 海关编码:
    2909199090
  • 包装等级:
    II
  • 危险类别:
    3.1
  • 安全说明:
    S16,S23,S33

SDS

SDS:3d2a3f0dcfbdaf73748991d70fddab90
查看
Name: Allyl 1 1 2 2-tetrafluoroethyl ether 99% Material Safety Data Sheet
Synonym: Non
CAS: 1428-33-7
Section 1 - Chemical Product MSDS Name:Allyl 1 1 2 2-tetrafluoroethyl ether 99% Material Safety Data Sheet
Synonym:Non

Section 2 - COMPOSITION, INFORMATION ON INGREDIENTS
CAS# Chemical Name content EINECS#
1428-33-7 Allyl 1,1,2,2-Tetrafluoroethyl ether 99% 215-847-3
Hazard Symbols: XI
Risk Phrases: 36/37/38

Section 3 - HAZARDS IDENTIFICATION
EMERGENCY OVERVIEW
Irritating to eyes, respiratory system and skin.The toxicological properties of this material have not been fully investigated.
Potential Health Effects
Eye:
May cause eye irritation.
Skin:
May cause skin irritation.
Ingestion:
The toxicological properties of this substance have not been fully investigated. May be harmful if swallowed.
Inhalation:
The toxicological properties of this substance have not been fully investigated. May be harmful if inhaled.
Chronic:
No information found.

Section 4 - FIRST AID MEASURES
Eyes: Flush eyes with plenty of water for at least 15 minutes, occasionally lifting the upper and lower lids. Get medical aid immediately.
Skin:
Get medical aid immediately. Flush skin with plenty of soap and water for at least 15 minutes while removing contaminated clothing and shoes.
Ingestion:
If victim is conscious and alert, give 2-4 cupfuls of milk or water.
Get medical aid immediately.
Inhalation:
Get medical aid immediately. Remove from exposure to fresh air immediately. If not breathing, give artificial respiration. If breathing is difficult, give oxygen.
Notes to Physician:
Treat symptomatically.

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.
Extinguishing Media:
Use dry sand or earth to smother fire. Use water spray to cool fire-exposed containers.
Autoignition Temperature: Not available.
Flash Point: Not available.
NFPA Rating: Not published.
Explosion Limits, Lower: Not available.
Upper: Not available.

Section 6 - ACCIDENTAL RELEASE MEASURES
General Information: Use proper personal protective equipment as indicated in Section 8.
Spills/Leaks:
Absorb spill with inert material, (e.g., dry sand or earth), then place into a chemical waste container.

Section 7 - HANDLING and STORAGE
Handling:
Wash thoroughly after handling. Remove contaminated clothing and wash before reuse. Avoid contact with skin and eyes. Avoid ingestion and inhalation. Use only in a chemical fume hood.
Storage:
Keep away from heat, sparks, and flame. Store in a cool, dry place.

Section 8 - EXPOSURE CONTROLS, PERSONAL PROTECTION
Engineering Controls:
Use adequate general or local, explosion-proof ventilation to keep airborne levels to acceptable levels.
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.
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 29CFR 1910.134. Always use a NIOSH-approved respirator when necessary.

Section 9 - PHYSICAL AND CHEMICAL PROPERTIES

Physical State: Not available.
Appearance: Not available.
Odor: Not available.
pH: Not available.
Vapor Pressure: Not available.
Vapor Density: Not available.
Evaporation Rate: Not available.
Viscosity: Not available.
Boiling Point: Not available.
Freezing/Melting Point: Not available.
Decomposition Temperature: Not available.
Solubility: Not available.
Specific Gravity/Density: Not available.
Molecular Formula: Not available.
Molecular Weight: Not available.

Section 10 - STABILITY AND REACTIVITY
Chemical Stability:
Has not been fully evaluated.
Conditions to Avoid:
Light, excess heat.
Incompatibilities with Other Materials:
Oxidizing agents.
Hazardous Decomposition Products:
Carbon monoxide, carbon dioxide.
Hazardous Polymerization: Has not been reported

Section 11 - TOXICOLOGICAL INFORMATION
RTECS#:
CAS# 1428-33-7 unlisted.
LD50/LC50:
Not available.
Carcinogenicity:
Allyl 1,1,2,2-Tetrafluoroethyl ether - Not listed by ACGIH, IARC, NIOSH, NTP, or OSHA.
See actual entry in RTECS for complete information.

Section 12 - ECOLOGICAL INFORMATION
For further information, contact Fisher Scientific.

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

Section 14 - TRANSPORT INFORMATION

CDG/CPL
IMO
Not regulated as a hazardous material.
IATA
Not regulated as a hazardous material.
RID/ADR
Not regulated as a hazardous material.
Canadian TDG
No information available.

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:
WGK (Water Danger/Protection)
CAS# 1428-33-7:
Canada
None of the chemicals in this product are listed on the DSL/NDSL list.
WHMIS: Not available.
CAS# 1428-33-7 is not listed on Canada's Ingredient Disclosure List.
Exposure Limits
US FEDERAL
TSCA
CAS# 1428-33-7 is not listed on the TSCA inventory.
It is for research and development use only.


SECTION 16 - ADDITIONAL INFORMATION
N/A

反应信息

  • 作为反应物:
    描述:
    烯丙基-1,1,2,2-四氟乙基醚 在 dihydrogen hexachloroplatinate 二氯硅烷 作用下, 生成 Dichlor-<3-(1,1,2,2-tetrafluor-aethoxy)-propyl>-silan
    参考文献:
    名称:
    Ponomarenko,V.A. et al., Journal of applied chemistry of the USSR, 1960, vol. 33, p. 2714 - 2720
    摘要:
    DOI:
  • 作为产物:
    描述:
    四氟乙烯烯丙醇 在 sodium hydride 作用下, 以 四氢呋喃 为溶剂, 反应 6.0h, 生成 烯丙基-1,1,2,2-四氟乙基醚
    参考文献:
    名称:
    作为眼镜蛇毒磷脂酶 A2 抑制剂的磷脂类似物的合成和评价
    摘要:
    Synthese d'analogues de phosphatidylcholine ou le groupe situen en 2 est remplace par des oxo-2alkane ou des hydroxy-2烷基
    DOI:
    10.1021/ja00260a020
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文献信息

  • Process for preparing fluoroalkyl-containing organosilicon compounds,
    申请人:Huels Aktiengesellschaft
    公开号:US05869728A1
    公开(公告)日:1999-02-09
    Fluoroalkyl organosilicon compounds are prepared by reacting fluoroolefins with organosilicon compounds that contain at least one H--Si group, in the presence of a Pt(0) complex catalyst. Further, fluoroalkylalkoxy organosilicon compounds are prepared by esterifying fluoroalkyl organosilicon compounds. The process proceeds uniformly under mild conditions with high yields and selectivities.
    氟烷基有机硅化合物是通过在Pt(0)复合催化剂存在下,将含有至少一个H-Si基团的有机硅化合物与氟烯烃反应制备而成。此外,通过酯化氟烷基有机硅化合物,可以制备氟烷基烷氧基有机硅化合物。该过程在温和条件下均匀进行,产率和选择性高。
  • Kinetic Study for the Reactions of Several Hydrofluoroethers with Chlorine Atoms
    作者:Vassileios C. Papadimitriou、Kyriakos G. Kambanis、Yannis G. Lazarou、Panos Papagiannakopoulos
    DOI:10.1021/jp031081z
    日期:2004.4.1
    Arrhenius expressions for the studied reactions are (in cm3 molecule-1 s-1, 2σ uncertainties):  k1 = (5.49 ± 1.51) × 10-12 exp(−928 ± 155/T), k2 = (1.99 ± 0.12) × 10-12 exp(−36 ± 33/ T), k3 = (1.95 ± 0.72) × 10-12 exp(−1616 ± 202/T), k4 = (8.72 ± 2.93) × 10-12 exp(−1112 ± 186/T), and k5 = (5.54 ± 1.96) × 10-13 exp(821 ± 214/T). The title reactions proceed via hydrogen atom metathesis, with the exception of
    氯原子与氢氟醚 CHF2CF2OCH3 (1)、CHF2CF2OCH2CH3 (2)、CHF2CF2OCH2CF3 (3)、CF3CHFCF2OCH3 (4) 和 CH2CHCH2OCF2CHF2 (5) 的反应动力学在 273-363 K 温度范围内的气相中进行了研究。通过监测两种反应物,在配备有四极质谱仪的分子流系统中,在非常低的压力 (<3 mTorr) 下进行了实验。所研究反应的建议 Arrhenius 表达式为(cm3 分子-1 s-1,2σ 不确定性):k1 = (5.49 ± 1.51) × 10-12 exp(-928 ± 155/T), k2 = (1.99 ± 0.12 ) × 10-12 exp(-36 ± 33/T), k3 = (1.95 ± 0.72) × 10-12 exp(-1616 ± 202/T), k4 = (8.72 ± 2.93) × 10-12 exp(-
  • Preparative Flow Techniques; 1. Low-Temperature Organometallic Reactions: Synthesis of Ethyl 2,2-Difluoro-4-pentenoate
    作者:Michael Kolb、Fritz Gerhart、Jean-Paul François
    DOI:10.1055/s-1988-27608
    日期:——
    A convenient preparation of the synthetically useful ethyl 2,2-difluoro-4-pentenoate using the low-temperature flow technique is described. The method is suitable for small-scale as well as for large-scale application.
    本文介绍了使用低温流动技术合成有用的2,2-二氟-4-戊烯酸乙酯的便捷方法。该方法适用于小规模以及大规模应用。
  • Monakhova,A.T. et al., Journal of Organic Chemistry USSR (English Translation), 1969, vol. 5, p. 1884 - 1887
    作者:Monakhova,A.T. et al.
    DOI:——
    日期:——
  • Cyclizations of 5-Hexenyl, 6-Heptenyl, 7-Octenyl, and 8-Nonenyl Radicals. The Kinetic and Regiochemical Impact of Fluorine and Oxygen Substituents
    作者:Anrong Li、Alexander B. Shtarev、Bruce E. Smart、Zhen-Yu Yang、Janusz Lusztyk、Keith U. Ingold、Anna Bravo、William R. Dolbier
    DOI:10.1021/jo990544n
    日期:1999.8.1
    Using competition kinetic methodology, rate constants for cyclizations of a series of hydrofluorocarbon (HFC) and ether 5-hexenyl, 6-heptenyl, and 7-octenyl radicals have been determined. Remarkably large rate constants (>10(7) s(-1)) have been observed for 6-exo-cyclizations of 1,1,2,2-tetrafluoro- and 1,1,2,2,3,3,4,4,-octafluoro-6-heptenyl radicals (>10(3) those of analogous hydrocarbon radicals), whereas HFC hexenyl and heptenyl ethers exhibit lower cyclization reactivity, as do HFC 7-octenyl radical systems, which cyclize in an endo manner. HFC 8-nonenyl radicals were not observed to cyclize. The results can be rationalized in terms of transition state polar influences, though other factors may also play significant roles.
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