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草酸乙酯 | 1457-85-8

中文名称
草酸乙酯
中文别名
草酰苯胺乙酯
英文名称
Ethyl oxanilate
英文别名
oxo(phenylamino)-acetic acid, ethyl ester;ethyl 2-oxo-2-(phenylamino)acetate;ethyl 2-anilino-2-oxoacetate
草酸乙酯化学式
CAS
1457-85-8
化学式
C10H11NO3
mdl
MFCD00009118
分子量
193.202
InChiKey
YDGAUBHNAKCSKF-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:
    67-69 °C(lit.)
  • 沸点:
    329.41°C (rough estimate)
  • 密度:
    1.2307 (rough estimate)
  • 稳定性/保质期:
    如果按照规格使用和储存,则不会分解,未有已知危险反应。应避免与氧化物接触。

计算性质

  • 辛醇/水分配系数(LogP):
    1.5
  • 重原子数:
    14
  • 可旋转键数:
    4
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.2
  • 拓扑面积:
    55.4
  • 氢给体数:
    1
  • 氢受体数:
    3

安全信息

  • 安全说明:
    S24/25
  • WGK Germany:
    3
  • 海关编码:
    2924299090
  • 包装等级:
    III
  • 危险类别:
    9
  • 危险性防范说明:
    P260,P264,P273,P301+P312,P305+P351+P338,P314
  • 危险品运输编号:
    3077
  • 危险性描述:
    H302,H319,H372,H410
  • 储存条件:
    请将贮藏器密封,并存放在阴凉、干燥处。同时,确保工作环境具备良好的通风或排气设施。

SDS

SDS:f8e4b4504f9ff80076792c4abb633c02
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Name: Ethyl oxanilate 98% Material Safety Data Sheet
Synonym: None
CAS: 1457-85-8
Section 1 - Chemical Product MSDS Name:Ethyl oxanilate 98% Material Safety Data Sheet
Synonym:None

Section 2 - COMPOSITION, INFORMATION ON INGREDIENTS
CAS# Chemical Name content EINECS#
1457-85-8 Ethyl oxanilate 98 215-945-6
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:
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. 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# 1457-85-8: 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: white
Odor: none reported
pH: Not available.
Vapor Pressure: Not available.
Viscosity: Not available.
Boiling Point: Not available.
Freezing/Melting Point: 67.00 - 69.00 deg C
Autoignition Temperature: Not applicable.
Flash Point: Not applicable.
Explosion Limits, lower: Not available.
Explosion Limits, upper: Not available.
Decomposition Temperature: Not available.
Solubility in water: Not available.
Specific Gravity/Density: Not available.
Molecular Formula: C10H11NO3
Molecular Weight: 193.20

Section 10 - STABILITY AND REACTIVITY
Chemical Stability:
Stable under normal temperatures and pressures.
Conditions to Avoid:
Incompatible materials, strong oxidants.
Incompatibilities with Other Materials:
Oxidizing agents.
Hazardous Decomposition Products:
Nitrogen oxides, carbon monoxide, irritating and toxic fumes and gases, carbon dioxide.
Hazardous Polymerization: Has not been reported

Section 11 - TOXICOLOGICAL INFORMATION
RTECS#:
CAS# 1457-85-8 unlisted.
LD50/LC50:
Not available.
Carcinogenicity:
Ethyl oxanilate - 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
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.
WGK (Water Danger/Protection)
CAS# 1457-85-8: No information available.
Canada
None of the chemicals in this product are listed on the DSL/NDSL list.
CAS# 1457-85-8 is not listed on Canada's Ingredient Disclosure List.
US FEDERAL
TSCA
CAS# 1457-85-8 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:
    草酸乙酯五氯化磷 作用下, 以 甲苯 为溶剂, 反应 5.0h, 以54%的产率得到ethyl 2,2-dichloro-2-(phenylamino)acetate
    参考文献:
    名称:
    2-(芳氨基)-2-(芳亚氨基)乙酰胺的合成
    摘要:
    2-(芳基氨基)-2-氧代乙酸酯与PCl5反应得到2-(芳基氨基)-2,2-二氯乙酸酯。这些化合物与苯胺衍生物的反应允许方便地合成多种 2-(芳基氨基)-2-(芳基亚氨基)乙酰胺。(© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2004)
    DOI:
    10.1002/ejoc.200300625
  • 作为产物:
    描述:
    diethyl 2-(phenylamino)maleate叔丁基过氧化氢 作用下, 以 氯苯 为溶剂, 反应 2.0h, 以85%的产率得到草酸乙酯
    参考文献:
    名称:
    叔丁基过氧化氢促进缺电子烯胺的无金属氧化 C=C 键裂解
    摘要:
    描述了一种新型的叔丁基氢过氧化物 (TBHP) 促进的烯胺氧化 C=C 双键裂解。在 TBHP 存在下,将缺电子烯胺的氯苯溶液在 80°C 下加热两小时,导致 C=C 键断裂。本研究为利用 TBHP 形成 C=O 双键提供了一种新策略。
    DOI:
    10.1055/s-0036-1588990
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文献信息

  • Certain Nitrogen Containing Bicyclic Chemical Entities for Treating Viral Infections
    申请人:Baskaran Subramanian
    公开号:US20100204265A1
    公开(公告)日:2010-08-12
    Provided are certain chemical entities, pharmaceutical compositions, and methods of treatment of a member of the flaviviradae family of viruses such as hepacivirus (Hepatitis C or HCV).
    提供了一些化学实体、药物组合物以及治疗黄病毒科家族成员,如肝病毒(丙型肝炎或HCV)的方法。
  • Copper-Catalysed (Diacetoxyiodo)benzene-Promoted Aerobic Esterification Reaction: Synthesis of Oxamates from Acetoacetamides
    作者:Zhiguo Zhang、Xiaolong Gao、Haifeng Yu、Guisheng Zhang、Jianming Liu
    DOI:10.1002/adsc.201800616
    日期:2018.9.3
    A copper‐catalysed (diacetoxyiodo)benzene‐promoted aerobic esterification reaction of acetoacetamides was developed for the synthesis of oxamates, which are useful precursors in synthetic organic chemistry. This practical and mild synthetic approach proceeded at 25 °C under open‐air conditions and afforded methyl 2‐oxo‐2‐(phenylamino)acetates in good to excellent yields combined with C−C σ‐bond cleavage
    开发了铜催化(二乙酰氧基碘)苯促进的乙酰乙酰胺需氧酯化反应,以合成草酸盐,草酸盐在合成有机化学中是有用的前体。这种实用且温和的合成方法在露天条件下于25°C进行,提供了具有良好或优异收率的2-氧代-2-(苯基氨基)乙酸甲酯,并带有C-Cσ-键裂解和正式的C-H氧化键功能化。提出了一种机制。
  • Preparations of carboxylic acid esters containing heptafluoroisopropyl groups
    作者:T. Suyama、S. Kato、Y. Mizutani
    DOI:10.1016/s0022-1139(00)80184-0
    日期:1992.1
    fluoroglyoxylic acid esters and fluoroformic acid esters with perfluoropropene (PFP) yielded perfluoro(3-methyl-2-oxobutyric) acid esters and perfluoroisobutyric acid esters, respectively. Oxamide derivatives and 2,3-quinoxalinediol have been prepared by the reaction of perfluoro(3-methyl-2-oxobutyric) acid esters with amines and o- phenylenediamine, respectively. Perfluoro(3-methyl-2-oxobutyric) acid esters
    氟乙醛酸酯和氟甲酸酯与全氟丙烯(PFP)的反应分别生成了全氟(3-甲基-2-氧代丁酸)酸酯和全氟异丁酸酯。通过全氟(3-甲基-2-氧代丁酸)酸酯分别与胺和邻苯二胺反应制备了乙酰胺衍生物和2,3-喹喔啉二醇。全氟(3-甲基-2-氧代丁酸)酸酯在质子惰性溶剂中在氟离子存在下加热时得到全氟异丁酸酯。
  • 酰胺咪唑类衍生物及其用途
    申请人:沈阳药科大学
    公开号:CN105541828B
    公开(公告)日:2019-04-02
    本发明属于医药技术领域,涉及通式I所示的酰胺咪唑类衍生物,其立体异构体及其药学上可接受的盐、水合物、溶剂化物或前药,其中取代基R、R1、Ar、M、X具有在说明书中给出的定义。本发明还涉及制备式I化合物的方法、含有上述化合物的药用组合物以及上述化合物及药用组合物用于制备治疗和/或预防癌症和其它皮肤增生性疾病的药物中的用途。本发明化合物还经抗真菌实验发现,对各种浅部和深部真菌有较强的抗菌效果,可用于制备治疗抗真菌药物中的用途。(I)。
  • New Highlights in the Synthesis of 4-Aryl-1,4-dihydropyrazines
    作者:Jing-Yu He、Xiu-Qing Song、Hong Yan、Ru-Gang Zhong
    DOI:10.1002/jhet.989
    日期:2012.11
    The 4‐aryl‐1,4‐dihydropyrazines were prepared via the cyclization of N,N‐bisalkylated anilines with ammonium acetate. These reactions were aided by improvements in the synthesis of N,N‐bisalkylated anilines which were alkylated with anilines using ethyl 2‐diazo acetoacetate in a reaction catalyzed by rhodium acetate in the absence of oxygen. A possible mechanistic route is postulated on the basis of
    通过将N,N-双烷基化苯胺与乙酸铵环化来制备4-芳基-1,4-二氢吡嗪。这些反应得益于N,N-双烷基化苯胺的合成的改进,N2-N-双烷基化苯胺在无氧乙酸铑的催化下,使用乙酰丙酮-2-重氮乙酯与苯胺烷基化。推测可能的机理路线是基于N烷基化中间体的分离,该中间体经1 H NMR数据和X射线衍射确定为N芳基草酸酯。
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表征谱图

  • 氢谱
    1HNMR
  • 质谱
    MS
  • 碳谱
    13CNMR
  • 红外
    IR
  • 拉曼
    Raman
hnmr
mass
cnmr
ir
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  • 峰位数据
  • 峰位匹配
  • 表征信息
Shift(ppm)
Intensity
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Assign
Shift(ppm)
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测试频率
样品用量
溶剂
溶剂用量
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同类化合物

(甲基3-(二甲基氨基)-2-苯基-2H-azirene-2-羧酸乙酯) (±)-盐酸氯吡格雷 (±)-丙酰肉碱氯化物 (d(CH2)51,Tyr(Me)2,Arg8)-血管加压素 (S)-(+)-α-氨基-4-羧基-2-甲基苯乙酸 (S)-阿拉考特盐酸盐 (S)-赖诺普利-d5钠 (S)-2-氨基-5-氧代己酸,氢溴酸盐 (S)-2-[3-[(1R,2R)-2-(二丙基氨基)环己基]硫脲基]-N-异丙基-3,3-二甲基丁酰胺 (S)-1-(4-氨基氧基乙酰胺基苄基)乙二胺四乙酸 (S)-1-[N-[3-苯基-1-[(苯基甲氧基)羰基]丙基]-L-丙氨酰基]-L-脯氨酸 (R)-乙基N-甲酰基-N-(1-苯乙基)甘氨酸 (R)-丙酰肉碱-d3氯化物 (R)-4-N-Cbz-哌嗪-2-甲酸甲酯 (R)-3-氨基-2-苄基丙酸盐酸盐 (R)-1-(3-溴-2-甲基-1-氧丙基)-L-脯氨酸 (N-[(苄氧基)羰基]丙氨酰-N〜5〜-(diaminomethylidene)鸟氨酸) (6-氯-2-吲哚基甲基)乙酰氨基丙二酸二乙酯 (4R)-N-亚硝基噻唑烷-4-羧酸 (3R)-1-噻-4-氮杂螺[4.4]壬烷-3-羧酸 (3-硝基-1H-1,2,4-三唑-1-基)乙酸乙酯 (2S,3S,5S)-2-氨基-3-羟基-1,6-二苯己烷-5-N-氨基甲酰基-L-缬氨酸 (2S,3S)-3-((S)-1-((1-(4-氟苯基)-1H-1,2,3-三唑-4-基)-甲基氨基)-1-氧-3-(噻唑-4-基)丙-2-基氨基甲酰基)-环氧乙烷-2-羧酸 (2S)-2,6-二氨基-N-[4-(5-氟-1,3-苯并噻唑-2-基)-2-甲基苯基]己酰胺二盐酸盐 (2S)-2-氨基-3-甲基-N-2-吡啶基丁酰胺 (2S)-2-氨基-3,3-二甲基-N-(苯基甲基)丁酰胺, (2S,4R)-1-((S)-2-氨基-3,3-二甲基丁酰基)-4-羟基-N-(4-(4-甲基噻唑-5-基)苄基)吡咯烷-2-甲酰胺盐酸盐 (2R,3'S)苯那普利叔丁基酯d5 (2R)-2-氨基-3,3-二甲基-N-(苯甲基)丁酰胺 (2-氯丙烯基)草酰氯 (1S,3S,5S)-2-Boc-2-氮杂双环[3.1.0]己烷-3-羧酸 (1R,4R,5S,6R)-4-氨基-2-氧杂双环[3.1.0]己烷-4,6-二羧酸 齐特巴坦 齐德巴坦钠盐 齐墩果-12-烯-28-酸,2,3-二羟基-,苯基甲基酯,(2a,3a)- 齐墩果-12-烯-28-酸,2,3-二羟基-,羧基甲基酯,(2a,3b)-(9CI) 黄酮-8-乙酸二甲氨基乙基酯 黄荧菌素 黄体生成激素释放激素 (1-5) 酰肼 黄体瑞林 麦醇溶蛋白 麦角硫因 麦芽聚糖六乙酸酯 麦根酸 麦撒奎 鹅膏氨酸 鹅膏氨酸 鸦胆子酸A甲酯 鸦胆子酸A 鸟氨酸缩合物