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4-十二烷氧基苯乙酮 | 2175-80-6

中文名称
4-十二烷氧基苯乙酮
中文别名
4-十二基氧基苯乙酮
英文名称
1-(4-dodecyloxy-phenyl)-ethanone
英文别名
4-dodecyloxyacetophenone;Acetophenone, 4'-(dodecyloxy)-;1-(4-dodecoxyphenyl)ethanone
4-十二烷氧基苯乙酮化学式
CAS
2175-80-6
化学式
C20H32O2
mdl
——
分子量
304.473
InChiKey
KOWOOZSAKAPHCW-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:
    44-47 °C
  • 沸点:
    405.28°C (rough estimate)
  • 密度:
    0.9659 (rough estimate)
  • 稳定性/保质期:
    在常温常压下保持稳定,应避免与不相容的材料接触。

计算性质

  • 辛醇/水分配系数(LogP):
    7.3
  • 重原子数:
    22
  • 可旋转键数:
    13
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.65
  • 拓扑面积:
    26.3
  • 氢给体数:
    0
  • 氢受体数:
    2

安全信息

  • 安全说明:
    S24/25
  • 海关编码:
    2914509090
  • 储存条件:
    密封储存,应存放于阴凉、干燥的库房中。

SDS

SDS:2455d067e8ea0b507debeb3e5109d422
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Name: 4 -Dodecyloxyacetophenone 94% (GC) Material Safety Data Sheet
Synonym: Ethanone, 1-(4-(Dodecyloxy)phenyl)-
CAS: 2175-80-6
Section 1 - Chemical Product MSDS Name:4 -Dodecyloxyacetophenone 94% (GC) Material Safety Data Sheet
Synonym:Ethanone, 1-(4-(Dodecyloxy)phenyl)-

Section 2 - COMPOSITION, INFORMATION ON INGREDIENTS
CAS# Chemical Name content EINECS#
2175-80-6 4'-Dodecyloxyacetophenone 94 unlisted
Hazard Symbols: None Listed.
Risk Phrases: None Listed.

Section 3 - HAZARDS IDENTIFICATION
EMERGENCY OVERVIEW
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:
May cause irritation of the digestive tract. The toxicological properties of this substance have not been fully investigated.
Inhalation:
May cause respiratory tract irritation. The toxicological properties of this substance have not been fully investigated.
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 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.
Notes to Physician:

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 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:
Clean up spills immediately, observing precautions in the Protective Equipment section. Sweep up, then place into a suitable container for disposal. Avoid generating dusty conditions. Provide ventilation.

Section 7 - HANDLING and STORAGE
Handling:
Wash thoroughly after handling. Remove contaminated clothing and wash before reuse. Use with adequate ventilation. Minimize dust generation and accumulation. Avoid contact with eyes, skin, and clothing. Keep container tightly closed. Avoid ingestion and inhalation.
Storage:
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 adequate ventilation to keep airborne concentrations low.
Exposure Limits CAS# 2175-80-6: 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: Powder
Color: light beige
Odor: None reported.
pH: Not available.
Vapor Pressure: Not available.
Viscosity: Not available.
Boiling Point: Not available.
Freezing/Melting Point: 44.00 - 47.00 deg C
Autoignition Temperature: Not applicable.
Flash Point: Not applicable.
Explosion Limits, lower: Not available.
Explosion Limits, upper: Not available.
Decomposition Temperature:
Solubility in water:
Specific Gravity/Density:
Molecular Formula: C20H32O2
Molecular Weight: 304.46

Section 10 - STABILITY AND REACTIVITY
Chemical Stability:
Stable under normal temperatures and pressures.
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# 2175-80-6: AM8485650 LD50/LC50:
CAS# 2175-80-6: Oral, mouse: LD50 = >2 gm/kg.
Carcinogenicity:
4'-Dodecyloxyacetophenone - Not listed by ACGIH, IARC, or NTP.
Other:
See actual entry in RTECS for complete information.

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
Not regulated as a hazardous material.
IMO
Not regulated as a hazardous material.
RID/ADR
Not regulated as a hazardous material.

Section 15 - REGULATORY INFORMATION

European/International Regulations
European Labeling in Accordance with EC Directives
Hazard Symbols: Not available.
Risk Phrases:
Safety Phrases:
S 24/25 Avoid contact with skin and eyes.
S 28A After contact with skin, wash immediately with
plenty of water.
S 37 Wear suitable gloves.
S 45 In case of accident or if you feel unwell, seek
medical advice immediately (show the label where
possible).
WGK (Water Danger/Protection)
CAS# 2175-80-6: No information available.
Canada
None of the chemicals in this product are listed on the DSL/NDSL list.
CAS# 2175-80-6 is not listed on Canada's Ingredient Disclosure List.
US FEDERAL
TSCA
CAS# 2175-80-6 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:
    4-十二烷氧基苯乙酮盐酸羟胺sodium ethanolate一水合肼溶剂黄146 作用下, 以 四氢呋喃乙醇 为溶剂, 反应 54.0h, 生成 (E)-N'-benzylidene-5-(4-(dodecyloxy)phenyl)isoxazole-3-carbohydrazide
    参考文献:
    名称:
    介晶杂环吡唑,异恶唑和1,3,4-恶二唑
    摘要:
    三个新的系列液晶的1 - 3报告了从杂环吡唑,异恶唑并呈现层列A 1,3,4-恶二唑或C相的。化合物1a表现出单向性近晶A相,而其他两种化合物2-3a不是介晶的。相反,所有其他具有较长烷氧基链的化合物1-3b均表现出近晶X和C相,这已通过粉末XRD衍射仪得到证实。清除温度按化合物1b  >  2b  >  3b的顺序降低,而近晶C相的温度范围按化合物1b  <  2b的顺序增加 <  3b。在近晶相1 -图3b是由一单体结构形成,确认并用粉末X射线衍射数据是一致的。介晶行为的形成可能归因于它们的环外角和/或H键。在TGA分析中,所有衍生物在低于T = 346°C的温度下均表现出良好的稳定性。
    DOI:
    10.1016/j.tet.2017.02.011
  • 作为产物:
    描述:
    溴代十二烷高氯酸potassium carbonate 作用下, 以 丙酮 为溶剂, 反应 8.5h, 生成 4-十二烷氧基苯乙酮
    参考文献:
    名称:
    Liquid crystalline N-aryl-β-aminovinyl ketones and their complexes with lanthanides
    摘要:
    Liquid crystalline lanthanide complexes with N-aryl-substituted beta-aminovinyl ketones were synthesized for the first time. The complexes give rise to smectic A mesophase and are stable only in the solid state; in going to solution, they dissociate with formation of the initial ligand.
    DOI:
    10.1134/s1070363206070152
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文献信息

  • Mesogenic heterocycles formed by bis-pyrazoles and bis-1,3,4-oxadiazoles
    作者:Kuan-Ting Lin、Gene-Hsiang Lee、Chung K. Lai
    DOI:10.1016/j.tet.2015.04.055
    日期:2015.6
    Three new series of compounds 1a–c containing multiple heterocyclic 2,5-pyrazoles, 1,3,4-oxadiazole and thiophene exhibiting mesophases were reported. Crystallographic data showed that the crystal 1a (n=8) is a linear-shaped molecule with a molecular length of ca. 40.57 Å. However, three heterocyclic rings were not coplanar. All compounds 1a formed smectic A/C phases, and all compounds 1c exhibited columnar
    报道了三个新的系列化合物1a – c,其中包含多个显示中间相的杂环2,5,5-吡唑,1,3,4-恶二唑和噻吩。晶体学数据表明,晶体1a(n = 8)是线型分子,分子长为。40.57Å。但是,三个杂环不是共面的。所有化合物1a均形成近晶A / C相,并且所有化合物1c均显示出柱状相,这通过粉末X射线衍射仪(XRD)证实。对于导数1c,在9.0埃厚的切片中获得了一个N电池,R ar值等于3.91和18.29Å(n = 8),表明在Col h相的列内两个分子是相关的。通过热重分析(TGA),所有衍生物在T = 383–426°C以下的温度下均表现出良好的稳定性。所有化合物的PL光谱图1b - Ç(Ñ = 8)显示出一个强峰在λ最大= 428-496纳米,且这些光致发光发射(PL)源自1,3,4-恶二唑基部分。
  • 2-Phenyl-indole derivatives and process for preparing the same
    申请人:Labaz
    公开号:US04057530A1
    公开(公告)日:1977-11-08
    New stabilizers of polymers and co-polymers of vinyl chloride, the said stabilizers being 2-phenyl-indole derivatives corresponding to the formula: ##STR1## wherein R represents a phenyl radical, an amino group, optionally substituted by an acetyl or benzoyl radical, a mercapto group, optionally substituted by a branched-or straight-chain alkyl group containing from 1 to 12 carbon atoms or by a cyclohexyl radical, a carboxyl radical, a radical represented by the formula: R.sub.1 O-- wherein R.sub.1 represents a hydrogen atom, an isopropyl, carboxymethyl, carbethoxymethyl, carbethoxyisopropyl, acetyl, docosanoyl, benzoyl, benzyl, or allyl radical or a branched-or straight-chain alkyl radical containing from 6 to 12 carbon atoms.
    新型稳定剂用于聚合物和氯乙烯共聚物,所述稳定剂为与下式对应的2-苯基吲哚衍生物:##STR1## 其中R代表苯基基团,氨基团,可选地由乙酰基或苯甲酰基取代,巯基,可选地由含有1至12个碳原子的支链或直链烷基基团或环己基基团取代,羧基基团,由下式表示的基团:R.sub.1 O--其中R.sub.1代表氢原子,异丙基,羧甲基,羧乙氧甲基,羧乙氧异丙基,乙酰基,二十二烷酰基,苯甲酰基,苄基或烯丙基基团或含有6至12个碳原子的支链或直链烷基基团。
  • Fluorescent columnar bis(boron difluoride) complexes derived from tetraketonates
    作者:Ya-Wen Chen、Yen-Chun Lin、Hsiu-Ming Kuo、Chung K. Lai
    DOI:10.1039/c7tc01425b
    日期:——
    of bis-(boron difluoride) complexes 1a–c derived from substituted tetraketonates 2a–c are reported, and their mesomorphic and optical properties have been investigated. Two single crystals of mesogenic ligand 2a (n = 6) and nonmesogenic diboron complex 1a (n = 14) were obtained, and their single crystal and molecular structures were resolved. Results show that all 2a ligands (n = 6, 8, 10, 12, 14) formed
    据报道,由取代的四酮酸酯2a-c衍生出三个新的双-(二氟化硼)配合物1a-c系列,并研究了它们的介晶和光学性质。获得了两个介晶配体2a(n = 6)和非介晶二硼配合物1a(n = 14)的单晶,并解析了它们的单晶和分子结构。结果表明,所有2a配体(n = 6、8、10、12、14)均形成向列和/或近晶C相。但是,所有2b–c化合物都不是介晶的。相反,bis(BF 2)络合物1a–b是非介晶的,1c(n = 8、10、12)表现出对映体柱状中间相。对于化合物1c,在9.0埃厚的柱层中获得了N cell = 2.70–2.86 ,这表明在Col h相中,单个盘状分子堆叠在柱中。在室温下,Bis(BF 2)络合物1a–c(n = 8)在溶液中具有明显的黄红色发射。发光发射显示对结构部分有很强的依赖性结合,与λ最大= 538(1A)<641(图1b)<708纳米(1C)。据我们所知,这是柱状bis(BF
  • 5-(Tetradecyloxy)-2-furancarboxylic acid and related hypolipidemic fatty acid-like alkyloxyarylcarboxylic acids
    作者:Roger A. Parker、Takashi Kariya、J. Martin Grisar、Vladimir Petrow
    DOI:10.1021/jm00216a009
    日期:1977.6
    5-(Tetradecyloxy)-2-furancarboxylic acid (91, RMI 14514) was found to lower blood lipids and to inhibit fatty acid synthesis with minimal effects on liver weight and liver fat content. This fatty acid-like compound represents a new class of hypolipidemic agent; it is effective in rats and monkeys. The compound resulted from discovery of hypolipidemic activity in certain beta-keto esters, postulation
    发现5-(四氢癸氧基)-2-呋喃羧酸(91,RMI 14514)可以降低血脂并抑制脂肪酸合成,对肝脏重量和肝脏脂肪含量的影响最小。这种类似脂肪酸的化合物代表了一类新的降血脂药。对大鼠和猴子有效。该化合物的产生是由于发现了某些β-酮酸酯的降血脂活性,假定和确认了相应的苯甲酸作为活性代谢物以及系统地研究了结构-活性关系。
  • Synthesis, Characterization, and Mesomorphic Properties of New Pyridine Derivatives
    作者:Ahipa T. N.
    DOI:10.1002/open.201500158
    日期:2015.12
    Luminescent liquid crystals have received significant research interest due to their wide range of applications. Here, new pyridine derivatives were designed as liquid crystalline materials. They were successfully synthesized via appropriate synthetic routes, their structures confirmed by various spectral techniques, and finally characterized for their mesogenic, optical and optoelectronic properties
    发光液晶由于其广泛的应用而受到了广泛的研究兴趣。在这里,新的吡啶衍生物被设计为液晶材料。它们是通过适当的合成路线成功合成的,其结构已通过各种光谱技术证实,并最终通过介晶,光学和光电特性进行了表征。
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