摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

咪唑并[1,2-a]嘧啶-2-甲酸乙酯 | 64951-06-0

中文名称
咪唑并[1,2-a]嘧啶-2-甲酸乙酯
中文别名
咪唑[1,2-A]嘧啶-2-甲酸乙酯;Ethy咪唑[1,2-a]嘧啶-2-羧酸;咪唑[1,2-a]嘧啶-2-羧酸乙酯
英文名称
ethyl imidazo[1,2-a]pyrimidine-2-carboxylate
英文别名
ethyl imidazo<1,2-a>pyrimidine-2-carboxylate
咪唑并[1,2-a]嘧啶-2-甲酸乙酯化学式
CAS
64951-06-0
化学式
C9H9N3O2
mdl
MFCD02186164
分子量
191.189
InChiKey
SORASSFGEFQWIH-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:
    170-172°
  • 密度:
    1.33±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    1.7
  • 重原子数:
    14
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.222
  • 拓扑面积:
    56.5
  • 氢给体数:
    0
  • 氢受体数:
    4

安全信息

  • 危险等级:
    IRRITANT
  • 海关编码:
    2933990090
  • 危险性防范说明:
    P261,P280,P305+P351+P338
  • 危险性描述:
    H302,H315,H319,H332,H335
  • 储存条件:
    室温且干燥环境下使用。

SDS

SDS:4c682c577cf5c8bd6a39cdb0ed5f4340
查看
Material Safety Data Sheet

Section 1. Identification of the substance
Product Name: Ethyl imidazo[1,2-a]pyrimidine-2-carboxylate
Synonyms:

Section 2. Hazards identification
Harmful by inhalation, in contact with skin, and if swallowed.

Section 3. Composition/information on ingredients.
Ingredient name: Ethyl imidazo[1,2-a]pyrimidine-2-carboxylate
CAS number: 64951-06-0

Section 4. First aid measures
Skin contact: Immediately wash skin with copious amounts of water for at least 15 minutes while removing
contaminated clothing and shoes. If irritation persists, seek medical attention.
Eye contact: Immediately wash skin with copious amounts of water for at least 15 minutes. Assure adequate
flushing of the eyes by separating the eyelids with fingers. If irritation persists, seek medical
attention.
Inhalation: Remove to fresh air. In severe cases or if symptoms persist, seek medical attention.
Ingestion: Wash out mouth with copious amounts of water for at least 15 minutes. Seek medical attention.

Section 5. Fire fighting measures
In the event of a fire involving this material, alone or in combination with other materials, use dry
powder or carbon dioxide extinguishers. Protective clothing and self-contained breathing apparatus
should be worn.

Section 6. Accidental release measures
Personal precautions: Wear suitable personal protective equipment which performs satisfactorily and meets local/state/national
standards.
Respiratory precaution: Wear approved mask/respirator
Hand precaution: Wear suitable gloves/gauntlets
Skin protection: Wear suitable protective clothing
Eye protection: Wear suitable eye protection
Methods for cleaning up: Mix with sand or similar inert absorbent material, sweep up and keep in a tightly closed container
for disposal. See section 12.
Environmental precautions: Do not allow material to enter drains or water courses.

Section 7. Handling and storage
Handling: This product should be handled only by, or under the close supervision of, those properly qualified
in the handling and use of potentially hazardous chemicals, who should take into account the fire,
health and chemical hazard data given on this sheet.
Store in closed vessels, refrigerated.
Storage:

Section 8. Exposure Controls / Personal protection
Engineering Controls: Use only in a chemical fume hood.
Personal protective equipment: Wear laboratory clothing, chemical-resistant gloves and safety goggles.
General hydiene measures: Wash thoroughly after handling. Wash contaminated clothing before reuse.

Section 9. Physical and chemical properties
Appearance: Not specified
Boiling point: No data
No data
Melting point:
Flash point: No data
Density: No data
Molecular formula: C9H9N3O2
Molecular weight: 191.2

Section 10. Stability and reactivity
Conditions to avoid: Heat, flames and sparks.
Materials to avoid: Oxidizing agents.
Possible hazardous combustion products: Carbon monoxide, nitrogen oxides.

Section 11. Toxicological information
No data.

Section 12. Ecological information
No data.

Section 13. Disposal consideration
Arrange disposal as special waste, by licensed disposal company, in consultation with local waste
disposal authority, in accordance with national and regional regulations.

Section 14. Transportation information
Non-harzardous for air and ground transportation.

Section 15. Regulatory information
No chemicals in this material are subject to the reporting requirements of SARA Title III, Section
302, or have known CAS numbers that exceed the threshold reporting levels established by SARA
Title III, Section 313.


SECTION 16 - ADDITIONAL INFORMATION
N/A

上下游信息

  • 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:
    咪唑并[1,2-a]嘧啶-2-甲酸乙酯ammonium hydroxide 作用下, 以 甲醇 为溶剂, 反应 3.0h, 以62%的产率得到咪唑并[1,2-a]嘧啶-2-甲酰胺
    参考文献:
    名称:
    Abignente; Arena; de Caprariis, Farmaco, Edizione Scientifica, 1980, vol. 35, # 8, p. 654 - 673
    摘要:
    DOI:
  • 作为产物:
    描述:
    丙酮酸乙酯 作用下, 以 1,4-二氧六环乙二醇二甲醚乙醚 为溶剂, 反应 49.0h, 生成 咪唑并[1,2-a]嘧啶-2-甲酸乙酯
    参考文献:
    名称:
    某些咪唑并[1,2-a]嘧啶衍生物的合成及抑菌活性。
    摘要:
    合成了75种咪唑并[1,2-a]嘧啶衍生物。据报道,这些化合物及其相应的α-溴代酮对多种革兰氏(+),革兰氏(-)细菌和分枝杆菌属物种具有“体外”抗菌活性。一些制备的衍生物表现出有效的抗微生物活性。
    DOI:
    10.1248/cpb.40.1170
点击查看最新优质反应信息

文献信息

  • Inexpensive Radical Methylation and Related Alkylations of Heteroarenes
    作者:Qi Huang、Samir Z. Zard
    DOI:10.1021/acs.orglett.8b00190
    日期:2018.3.2
    A simple method for the introduction of a methyl and higher aliphatic group to various heteroarenes using very inexpensive reagents is described. It is based on the radical addition of a carboxylic xanthate followed by decarboxylation. Depending on the heteroarene structure, the decarboxylation can be spontaneous or induced by heating in N,N-dimethylacetamide or N-methyl pyrrolidone in a microwave
    描述了一种使用非常便宜的试剂将甲基和高级脂肪族基团引入各种杂芳烃的简单方法。它基于羧酸黄原酸酯的自由基加成,然后进行脱羧。取决于杂芳烃结构,脱羧可以是自发的,或者可以通过在微波炉中的N,N-二甲基乙酰胺或N-甲基吡咯烷酮中加热来引发。
  • [EN] THERAPEUTIC INHIBITORY COMPOUNDS<br/>[FR] COMPOSÉS INHIBITEURS THÉRAPEUTIQUES
    申请人:LIFESCI PHARMACEUTICALS INC
    公开号:WO2018011628A1
    公开(公告)日:2018-01-18
    Provided herein are heterocyclic derivative compounds and pharmaceutical compositions comprising said compounds that are useful for inhibiting plasma kallikrein. Furthermore, the subject compounds and compositions are useful for the treatment of diseases wherein the inhibition of plasma kallikrein inhibition has been implicated, such as angioedema and the like.
    本文提供了杂环衍生物化合物和包含这些化合物的药物组合物,用于抑制血浆激肽酶。此外,这些化合物和组合物对于治疗血浆激肽酶抑制已被证实有关的疾病,如血管性水肿等,具有益处。
  • Story of an Age-Old Reagent: An Electrophilic Chlorination of Arenes and Heterocycles by 1-Chloro-1,2-benziodoxol-3-one
    作者:Mengzhou Wang、Yanyan Zhang、Tao Wang、Chao Wang、Dong Xue、Jianliang Xiao
    DOI:10.1021/acs.orglett.6b00547
    日期:2016.5.6
    By the use of 1-chloro-1,2-benziodoxol-3-one, an age-old reagent, the practical and efficient chlorination method is achieved. This hypervalent iodine reagent is amenable not only to the chlorination of nitrogen-containing heterocycles but also to selected classes of arenes, BODIPY dyes, and pharmaceuticals. In addition, the advantages, such as easy preparation and recyclable, air- and moisture-stable
    通过使用一种古老的试剂1-chloro-1,2-benziodoxol-3-one,可以实现一种实用而有效的氯化方法。这种高价碘试剂不仅适用于含氮杂环的氯化反应,而且适用于某些类别的芳烃,BODIPY染料和药物。另外,诸如易于制备和可回收利用,对空气和水分稳定的优点等优点,以及在克级实验中的成功,使该试剂具有巨大的工业应用潜力。
  • A Chlorinating Reagent: N-chloro-N-methoxybenzene Sulfonamide
    作者:Xiaoqiu Pu、Qingwei Li、Zehai Lu、Xianjin Yang
    DOI:10.1002/ejoc.201601226
    日期:2016.11
    Abstract: A structurally simple and reactive chlorinating reagent,N-chloro-N-methoxybenzenesulfonamide, was conveniently and economically prepared in high yield. 1,3-Diketones, β-keto esters, benzoyl trifluoroacetones, phenols, anisoles, heteroarenes andaromatic amines were chlorinated with it, obtaining chlorinated products in good to high yields.
    摘要: 一种结构简单、反应灵敏的氯化试剂N-氯-N-甲氧基苯磺酰胺可以方便、经济、收率高的制备。用它氯化1,3-二酮、β-酮酯、苯甲酰三氟丙酮、苯酚、苯甲醚、杂芳烃和芳香胺,得到氯化产物,收率高。
  • CFBSA: a novel and practical chlorinating reagent
    作者:Zehai Lu、Qingwei Li、Minghua Tang、Panpan Jiang、Hao Zheng、Xianjin Yang
    DOI:10.1039/c5cc05052a
    日期:——

    A novel chlorinating reagent was synthesized from easily-obtained materials and it shows great reactivity to a large scope of substrates.

    一个新型氯化试剂是由易得材料合成的,对广泛范围的底物表现出很高的反应性。
查看更多

同类化合物

法西普隆 咪唑并[1,2-a]嘧啶-7-基甲醇 咪唑并[1,2-a]嘧啶-3-醇 咪唑并[1,2-a]嘧啶-3-甲醛 咪唑并[1,2-a]嘧啶-2-胺 咪唑并[1,2-a]嘧啶-2-甲醛 咪唑并[1,2-a]嘧啶-2-甲酸乙酯 咪唑并[1,2-a]嘧啶-2-甲酰氯 咪唑并[1,2-a]嘧啶-2-基-甲基胺 咪唑并[1,2-a]嘧啶-2-基-乙酸乙酯 咪唑并[1,2-a]嘧啶-2-乙酸盐酸盐 咪唑并[1,2-a]嘧啶-2-乙腈 咪唑并[1,2-a]嘧啶 咪唑并[1,2-A]嘧啶-7-甲醛 咪唑并[1,2-A]嘧啶-6-胺盐酸盐 咪唑并[1,2-A]嘧啶-3-腈 咪唑并[1,2-A]嘧啶-3-羧酸乙酯 咪唑并[1,2-A]嘧啶-3-羧酸 咪唑[1,2-A]嘧啶-3-羧酸-2-甲基-甲酯 咪唑[1,2-A]嘧啶-2-羧酸 PTC-209抑制剂 7-甲氧基-5-甲基-2-(5-甲基-1,2,4-恶二唑-3-基)-6-丙基咪唑并[1,2-a]嘧啶 7-甲基咪唑并[1,2-a]嘧啶 7-氨基咪唑并[1,2-A]嘧啶 7-(三氟甲基)咪唑并[1,2-A]嘧啶 6-溴咪唑并[1,2-a]嘧啶-3-甲醛 6-溴咪唑并[1,2-a]嘧啶 6-溴咪唑并[1,2-A]嘧啶-3-羧酸 6-溴咪唑并[1,2-A]嘧啶-2-羧酸 6-溴-2-甲基咪唑并[1,2-a]嘧啶 6-氯咪唑[1,2-A]嘧啶 6-氟咪唑并[1,2-A]嘧啶-3-羧酸 6-异丙基咪唑并[1,2-a]嘧啶 6-乙基-7-甲氧基-5-甲基-2-(5-甲基-1,3,4-噻二唑-2-基)咪唑并[1,2-a]嘧啶 5-氯咪唑[1,2-a]嘧啶 5-氯-7-甲基咪唑[1,2-a]嘧啶 5-氨基咪唑并[1,2-A]嘧啶 5-氨基-7-氯咪唑并[1,2-a]嘧啶 5-哌啶-3-基-7-三氟甲基-咪唑并[1,2-a]-嘧啶二盐酸盐 5,7-二甲基咪唑并[1,2-a]嘧啶-2-羧酸 5,7-二甲基咪唑并[1,2-a]嘧啶 5,7-二氯咪唑并[1,2-A]嘧啶 3-硝基咪唑并[1,2-a]嘧啶 3-溴咪唑并[1,2-a]嘧啶 3-溴-咪唑并[1,2-a]嘧啶-2-羧酸乙酯 3-溴-7-甲基咪唑并[1,2-A]嘧啶 3-溴-7-(三氟甲基)咪唑并[1,2-a]嘧啶 3-溴-6-氯咪唑并[1,2-a]嘧啶 3-溴-5,7-二甲基咪唑并[1,2-a]嘧啶 3-溴-2-叔丁基咪唑并[1,2-a]嘧啶