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五氟苯基碳酸甲酯 | 36919-03-6

中文名称
五氟苯基碳酸甲酯
中文别名
柳胺苄心定
英文名称
methyl pentafluorophenyl carbonate
英文别名
methyl (2,3,4,5,6-pentafluorophenyl) carbonate
五氟苯基碳酸甲酯化学式
CAS
36919-03-6
化学式
C8H3F5O3
mdl
MFCD01075723
分子量
242.102
InChiKey
HGYOVHMDBHQLOE-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:
    24°C
  • 沸点:
    84°C 3mm
  • 密度:
    1.567±0.06 g/cm3(Predicted)
  • 闪点:
    84°C/3mm
  • 稳定性/保质期:
    常规情况下不会分解,没有危险反应。<?xml:namespace prefix = o ns = "urn:schemas-microsoft-com:office:office" />

计算性质

  • 辛醇/水分配系数(LogP):
    2.6
  • 重原子数:
    16
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.125
  • 拓扑面积:
    35.5
  • 氢给体数:
    0
  • 氢受体数:
    8

安全信息

  • 危险等级:
    6.1
  • 安全说明:
    S26,S36/37/39
  • 危险类别码:
    R22,R36/38
  • 海关编码:
    2920909090
  • 包装等级:
    III
  • 危险类别:
    6.1
  • 危险品运输编号:
    UN 2811
  • 危险性防范说明:
    P264,P280,P302+P352+P332+P313+P362+P364,P305+P351+P338+P337+P313
  • 危险性描述:
    H315,H319

SDS

SDS:f5890acfcb10f400243e1a971911b5b1
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Methyl Pentafluorophenyl Carbonate
SAFETY DATA SHEET

Section 1. IDENTIFICATION
Product name: Methyl Pentafluorophenyl Carbonate
5.3

Section 2. HAZARDS IDENTIFICATION
GHS classification
PHYSICAL HAZARDS Not classified
HEALTH HAZARDS
Skin corrosion/irritation Category 2
Category 2A
Serious eye damage/eye irritation
ENVIRONMENTAL HAZARDS Not classified
GHS label elements, including precautionary statements
Pictograms or hazard symbols
Signal word Warning
Hazard statements Causes skin irritation
Causes serious eye irritation
Precautionary statements:
Wash hands thoroughly after handling.
[Prevention]
Wear protective gloves/eye protection/face protection.
IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses,
[Response]
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.

Section 3. COMPOSITION/INFORMATION ON INGREDIENTS
Substance/mixture: Substance
Components: Methyl Pentafluorophenyl Carbonate
Percent: >98.0%(GC)
CAS Number: 36919-03-6
Synonyms: Carbonic Acid Methyl Pentafluorophenyl Ester
C8H3F5O3
Chemical Formula:

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.
Methyl Pentafluorophenyl Carbonate

Section 4. FIRST AID MEASURES
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.
Ingestion: Get medical advice/attention if you feel unwell. Rinse mouth.
A rescuer should wear personal protective equipment, such as rubber gloves and air-
Protection of first-aiders:
tight goggles.

Section 5. FIRE-FIGHTING MEASURES
Suitable extinguishing Dry chemical, foam, water spray, carbon dioxide.
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 Entry to non-involved personnel should be controlled around the leakage area by
emergency procedures: roping off, etc.
Environmental precautions: Prevent product from entering drains.
Methods and materials for Sweep dust to collect it into an airtight container, taking care not to disperse it.
containment and cleaning Adhered or collected material should be promptly disposed of, in accordance with
up: appropriate laws and regulations.

Section 7. HANDLING AND STORAGE
Precautions for safe handling
Technical measures: Handling is performed in a well ventilated place. Wear suitable protective equipment.
Prevent dispersion of dust. Wash hands and face thoroughly after handling.
Use a local exhaust if dust or aerosol will be generated.
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 and dark place.
Store away from incompatible materials such as oxidizing agents.
Packaging material: Comply with laws.

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: Dust 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): Solid
Crystal- Lump
Form:
Colour: White - Almost white
No data available
Odour:
Methyl Pentafluorophenyl Carbonate

Section 9. PHYSICAL AND CHEMICAL PROPERTIES
pH: No data available
Melting point/freezing point:34°C
Boiling point/range: 84°C/0.4kPa
Flash point: No data available
Flammability or explosive
limits:
Lower: No data available
Upper: No data available
Relative density: No data available
Solubility(ies):
[Water] No data available
[Other solvents] No data available

Section 10. STABILITY AND REACTIVITY
Chemical stability: Stable under proper conditions.
Possibility of hazardous No special reactivity has been reported.
reactions:
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:
No data available
IARC =
NTP = No data available
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
Bioaccumulative No data available
potential(BCF):
Mobility in soil
Log Pow: No data available
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 dissolve or mix material
with a 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.

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

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

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

反应信息

  • 作为反应物:
    描述:
    (R)-Carvone五氟苯基碳酸甲酯4-二甲氨基吡啶 、 magnesium bromide ethyl etherate 、 N,N-二异丙基乙胺 作用下, 以 二氯甲烷 为溶剂, 反应 48.0h, 以68%的产率得到(1S,6R)-methyl 3-methyl-6-(1-methylethenyl)-2-oxocyclohex-3-enecarboxylate
    参考文献:
    名称:
    酮烯醇盐C-酰化的一种新的温和方法。β-酮基酯,-硫代酸酯和-硫代酯的简便合成方法
    摘要:
    描述了一种新的酮烯醇C-酰化方法,该方法利用烷基五氟苯基碳酸酯,硫代碳酸酯和硫代碳酸氢酯作为反应性酰化剂,并使用MgBr 2 ·Et 2 O,DMAP和i -Pr 2 NEt作为烯醇化试剂。通过该方案,已经观察到各种各样的酮经历了清洁的C-酰化。
    DOI:
    10.1021/ol303324a
  • 作为产物:
    描述:
    五氟苯酚氯甲酸甲酯N-甲基吗啉 作用下, 以 二氯甲烷 为溶剂, 反应 1.0h, 以96%的产率得到五氟苯基碳酸甲酯
    参考文献:
    名称:
    酮烯醇盐C-酰化的一种新的温和方法。β-酮基酯,-硫代酸酯和-硫代酯的简便合成方法
    摘要:
    描述了一种新的酮烯醇C-酰化方法,该方法利用烷基五氟苯基碳酸酯,硫代碳酸酯和硫代碳酸氢酯作为反应性酰化剂,并使用MgBr 2 ·Et 2 O,DMAP和i -Pr 2 NEt作为烯醇化试剂。通过该方案,已经观察到各种各样的酮经历了清洁的C-酰化。
    DOI:
    10.1021/ol303324a
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文献信息

  • Concerted Mechanisms of the Reactions of Methyl Aryl Carbonates with Substituted Phenoxide Ions
    作者:Enrique A. Castro、Paulina Pavez、José G. Santos
    DOI:10.1021/jo010022j
    日期:2001.5.1
    respectively) with substituted phenoxide ions are subjected to a kinetic study in water at 25.0 degrees C, ionic strength 0.2 M (KCl). Production of the leaving groups (the nitro derivatives) is followed spectrophotometrically. Under excess of the phenoxide ions pseudo-first-order rate coefficients (k(obsd)) are found throughout. Plots of k(obsd) vs substituted phenoxide concentration at constant pH
    对4-硝基苯基,2,4-二硝基苯基和2,4,6-三硝基苯基碳酸甲基酯(分别为NPC,DNPC和TNPC)与取代的酚盐离子的反应在水中于25.0℃下进行动力学研究,离子强度0.2 M(KCl)。分光光度法测定离去基团(硝基衍生物)的产生。在过量的酚盐离子下,始终会发现伪一阶速率系数(k(obsd))。在恒定pH下,k(obsd)与取代的苯酚的浓度关系图呈线性关系,斜率(k(N))与pH无关。对于NPC,DNPC和TNPC的酚醛化作用,布朗斯台德型图(苯酚的log k(N)与pK(a))呈线性,斜率分别为β= 0.67、0.48和0.52。这些布朗斯台德斜率的大小与协调机制一致。在NPC发生酚醛化的特殊情况下,对于逐步机理而言,Brönsted图的预期假想曲率中心应为pK(a)(0)= 7.1(4-硝基苯酚的pK(a))。该曲率未出现在所研究的取代酚的pK(a)范围内(5.3--10.3),表
  • BIODEGRADABLE ORGANIC RADICAL-FUNCTIONALIZED POLYCARBONATES FOR MEDICAL APPLICATIONS
    申请人:International Business Machines Corporation
    公开号:US20160220705A1
    公开(公告)日:2016-08-04
    Paramagnetic, amphiphilic, biocompatible polymers were prepared comprising a carbonate repeat unit bearing a paramagnetic organic radical, more specifically a nitroxyl radical. The radical polymers can be produced in one step from a precursor polymer bearing an active ester side chain by treating the precursor polymer with a radical-bearing nucleophile. The precursor polymer can be prepared by organocatalyzed catalyzed ring opening polymerization (ROP) of a cyclic carbonate monomer bearing an active ester side chain. The radical polymers can be non-toxic and partially biodegradable. The radical polymers have utility as contrast enhancing agents in a medical imaging application and/or as therapeutic agents for treating a medical condition. The radical polymers can also serve as carriers for therapeutic agents (e.g., drugs) and/or medical image enhancing agents (e.g., NIRF dyes).
    具有顺磁性、两性亲疏性、生物相容性的聚合物已经制备好,其中包含一个带有顺磁性有机自由基的碳酸酯重复单元,更具体地说是一个亚硝基自由基。这种自由基聚合物可以通过将带有活性酯侧链的前体聚合物与带有自由基的亲核试剂处理而一步制备而成。前体聚合物可以通过有机催化的环氧化聚合(ROP)来制备,该环氧化单体带有活性酯侧链。这种自由基聚合物可能是无毒且部分可生物降解的。这种自由基聚合物在医学成像应用中可用作增强对比剂,和/或作为治疗医疗状况的治疗剂。这种自由基聚合物还可以作为治疗剂(例如药物)和/或医学图像增强剂(例如NIRF染料)的载体。
  • A New Stereocontrolled Synthetic Route to (−)-Echinosporin from <scp>d</scp>-Glucose via Padwa Allenylsulfone [3 + 2]-Anionic Cycloadditive Elimination
    作者:Jakub T. Flasz、Karl J. Hale
    DOI:10.1021/ol301090v
    日期:2012.6.15
    A new formal total synthesis of (−)-echinosporin has been developed based upon the Padwa [3 + 2]-cycloadditive elimination reaction of allenylsulfone 4 with the d-glucose-derived enone 14 which provides cycloadduct 12.
    ( - ) -的一种新形式的全合成echinosporin已经开发基于Padwa [3 + 2] allenylsulfone的-cycloadditive消去反应4与d葡萄糖衍生的烯酮14,其提供环加成12。
  • [EN] TREATMENT OF INFECTIONS<br/>[FR] TRAITEMENT D'INFECTIONS
    申请人:ASCENDIS PHARMA AS
    公开号:WO2020064844A1
    公开(公告)日:2020-04-02
    The present invention relates among other aspects to a conjugate or a pharmaceutically acceptable salt thereof or a pharmaceutical composition comprising said conjugate or its pharmaceutically acceptable salt for use in a method of preventing or treating an infection, wherein said conjugate is water-insoluble and comprises a polymeric moiety -Z to which a plurality of moieties -L2-X0D-L1-D are covalently conjugated, wherein each -D is independently an antibiotic moiety; each -L1- is independently a linker moiety to which -D is covalently and reversibly conjugated; each -X0D- is independently absent or a linkage and each -L2- is independently either a chemical bond or a spacer moiety.
    本发明涉及一种共轭物或其药用可接受的盐,或包含所述共轭物或其药用可接受的盐的药物组合物,用于预防或治疗感染的方法,其中所述共轭物不溶于水,包括一个聚合物基团-Z,其中多个基团-L2-X0D-L1-D以共价结合方式共轭,其中每个-D独立地是抗生素基团;每个-L1-独立地是连接基团,与-D以共价和可逆方式结合;每个-X0D-独立地不存在或是一个连接,每个-L2-独立地是化学键或间隔基团。
  • Antimicrobial ortho-Fluorophenyl Oxazolidinones For Treatment of Bacterial Infections
    申请人:Gordeev Mikhail Fedorovich
    公开号:US20090048305A1
    公开(公告)日:2009-02-19
    The present invention provides certain ortho-fluorophenyl oxazolidinones of the following formula I: or pharmaceutically acceptable salts or prodrugs thereof that are antibacterial agents, pharmaceutical compositions containing them, methods for their use, and methods for preparing these compounds.
    本发明提供了以下结构式I的某些邻氟苯基噁唑啉酮化合物,或其药用可接受的盐或前药,这些化合物是抗菌剂,包含它们的药物组合物,以及使用这些化合物的方法和制备这些化合物的方法。
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