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

3-溴异恶唑-5-甲酸乙酯 | 105174-97-8

中文名称
3-溴异恶唑-5-甲酸乙酯
中文别名
3-溴异唑-5-甲酸乙酯;3-溴异噁唑-5-甲酸乙酯
英文名称
3-Bromo-5-isoxazolecarboxylic Acid Ethyl Ester
英文别名
ethyl 3-bromoisoxazole-5-carboxylate;3-bromo-5-ethoxycarbonylisoxazole;ethyl 3-bromo-1,2-oxazole-5-carboxylate
3-溴异恶唑-5-甲酸乙酯化学式
CAS
105174-97-8
化学式
C6H6BrNO3
mdl
——
分子量
220.023
InChiKey
BLFWSORQDIUISI-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:
    279.1±20.0 °C(Predicted)
  • 密度:
    1.617±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    1.9
  • 重原子数:
    11
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.33
  • 拓扑面积:
    52.3
  • 氢给体数:
    0
  • 氢受体数:
    4

安全信息

  • 海关编码:
    2934999090
  • 危险性防范说明:
    P261,P305+P351+P338
  • 危险性描述:
    H302,H315,H319,H335

SDS

SDS:3034078c45163c1f026a60c8d169fa95
查看
Material Safety Data Sheet

Section 1. Identification of the substance
Product Name: Ethyl 3-bromoisoxazole-5-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 3-bromoisoxazole-5-carboxylate
CAS number: 105174-97-8

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, under −20◦C.
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: C6H6BrNO3
Molecular weight: 220

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, hydrogen bromide.

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:
    参考文献:
    名称:
    Process for the preparation of 3,5-disubstituted isoxazoles
    摘要:
    提供了一种制备3-溴-和3-氯-5-取代异噁唑的新工艺。在(i)至少等摩尔量的碱性碳酸钠和碳酸氢钾的类别中选择碱性碱,与二溴甲酰肟或二氯甲酰肟一起,在惰性溶剂中,在室温下与化学式为R-C.tbd.CH的1-炔基衍生物的过量反应,其中R为氢,苯基或1-6 C烷基,可选地被卤素,OH,OR',CHO,COR',COOR',CONH.sub.2,CONR'R"或NHCOR'取代,其中R'和R"可以相同或不同,是1-6 C烷基或卤代烷基。
    公开号:
    US04772719A1
  • 作为产物:
    描述:
    1,1-二溴甲醛肟丙炔酸乙酯 以68%的产率得到
    参考文献:
    名称:
    CHIARINO D.; NAPOLETANO M.; SALA A., J. HETEROCYCL. CHEM., 24,(1987) N 1, 45-46
    摘要:
    DOI:
点击查看最新优质反应信息

文献信息

  • [EN] AMIDINE SUBSTITUTED BETA - LACTAM COMPOUNDS, THEIR PREPARATION AND USE AS ANTIBACTERIAL AGENTS<br/>[FR] COMPOSÉS DE BÊTA-LACTAME À SUBSTITUTION AMIDINE, LEUR PRÉPARATION ET LEUR UTILISATION EN TANT QU'AGENTS ANTIBACTÉRIENS
    申请人:AICURIS GMBH & CO KG
    公开号:WO2013110643A1
    公开(公告)日:2013-08-01
    The present invention relates to novel β-lactam compounds of formula (I), their preparation and use. In particular, this invention relates to novel β-lactam compounds which are amidine substituted monobactam derivatives useful as antimicrobial agents and their preparation.
    本发明涉及式(I)的新型β-内酰胺化合物,它们的制备和使用。特别是,本发明涉及作为抗菌剂有用的新型β-内酰胺化合物,即取代脒的单巴坦衍生物及其制备方法。
  • Novel Heterocyclic Compounds as Pesticides
    申请人:MÜHLTHAU Friedrich August
    公开号:US20120094837A1
    公开(公告)日:2012-04-19
    The present invention relates to novel heterocyclic compounds, to processes for preparation thereof and to the use thereof for controlling animal pests, which include arthropods and especially insects.
    本发明涉及新颖的杂环化合物,其制备过程以及用于控制动物害虫的用途,包括节肢动物,尤其是昆虫。
  • 1,3-Dipolar cycloaddition synthesis of 3-bromo-5-substituted isoxazoles, useful intermediates for the preparation of pharmacologically active compounds
    作者:D. Chiarino、M. Napoletano、A. Sala
    DOI:10.1002/jhet.5570240109
    日期:1987.1
    monosubstituted acetylenic derivatives 4 to give 3-bromo-5-substituted isoxazoles 5 in high yield. The experimental conditions necessary to overcome difficulties such as the low reactivity of acetylenic dipolarophiles and the high tendency to dimerization of bromonitrile oxide 2, are discussed; the regioselectivity of this 1,3-dipolar cycloaddition is also studied. The obtained improvements in the synthesis of
    Bromonitrile氧化物2,从容易获得的二溴甲醛肟生成1,与单取代的炔属衍生物进行反应4,得到3-溴-5-异恶唑取代的5以高收率。讨论了克服困难的条件,例如乙炔双极性亲和剂的低反应性和溴代腈氧化物2的二聚化趋势高。还研究了这种1,3-偶极环加成反应的区域选择性。据报道在某些药理活性化合物的合成中获得的改进。
  • Pyrrol derivatives with antibacterial activity
    申请人:Green Morenike Oluyinka
    公开号:US20060223801A1
    公开(公告)日:2006-10-05
    Compounds of Formula (1) and their pharmaceutically acceptable salts are described: Formula (1) Processes for their preparation, pharmaceutical compositions containing them, their use as medicaments and their use in the treatment of bacterial infections are also described.
    本文描述了化学式(1)的化合物及其药用可接受的盐:化学式(1)。同时描述了其制备方法、含有它们的药物组合物、作为药物的用途以及在治疗细菌感染方面的应用。
  • AMIDINE SUBSTITUTED BETA-LACTAM COMPOUNDS, THEIR PREPARATION AND USE AS ANTIBACTERIAL AGENTS
    申请人:AiCuris GmbH & Co. KG
    公开号:US20150045340A1
    公开(公告)日:2015-02-12
    The present invention relates to novel β-lactam compounds, their preparation and use. In particular, this invention relates to novel β-lactam compounds which are amidine substituted monobactam derivatives useful as antimicrobial agents and their preparation.
    本发明涉及新型β-内酰胺化合物、它们的制备和用途。特别地,本发明涉及新型β-内酰胺化合物,其是取代了氨基甲酰基的单环内酰胺衍生物,可用作抗微生物剂,以及它们的制备。
查看更多

同类化合物

试剂2,5-Dibromo-3,4-dihexylthiophene 苯-1,2,4-三羧酸-丙烷-1,2,3-三醇(1:1) 碘吡咯 癸氯-二茂铁 溴代二茂铁 溴-(3-溴-2-噻嗯基)镁 派瑞林D 派瑞林 F 二聚体 氯代二茂铁 曲洛酯 异噻唑,3-氯-5-甲基- 地茂酮 四碘噻吩 四溴噻吩 四溴吡咯 四溴-N-甲基吡咯 四氯噻吩 四氟噻吩 噻菌腈 噻美尼定. 噻吩,3-溴-4-(1-辛炔基)- 噻吩,2,5-二氯-3,4-二(氯甲基)- 喷贝特 咪唑烷,2-(4-溴-5-甲基-2-呋喃基)-1,3-二甲基- 叔丁基2-溴-4,6-二氢-5H-吡咯并[3,4-D]噻唑-5-羧酸酯 叔-丁基2-溴-5,6-二氢咪唑并[1,2-A]吡嗪-7(8H)-甲酸基酯 八氟联苯烯 八氟二苯并硒吩 二苯基氯化碘盐 二联苯碘硫酸盐 二氯对二甲苯二聚体 二氯[2-甲基-3(2H)-异噻唑酮-O]的钙合物 二氯-1,2-二硫环戊烯酮 二-(3-溴-1,2,4-噻二唑-5-基)-二硫醚 二(2-噻吩基)碘鎓 [四丁基铵][Δ-三(四氯-1,2-苯二醇酸根)磷酸盐(V)] [3-(4-氯-3,5-二甲基-1H-吡唑-1-基)丙基]胺 [3-(4-氯-1H-吡唑-1-基)-2-甲基丙基]胺 [2-(4-溴-吡唑-1-基)-乙基]-二甲胺 [1-(4-溴-3-甲基-1,2-噻唑-5-基)乙亚基氨基]硫脲 [1-(4-溴-1,2-噻唑-3-基)乙亚基氨基]硫脲 [1,1'-联苯]-2,2'-二基碘鎓 [(4-碘-1,2-噻唑-5-基)亚甲基氨基]硫脲 [(4-氯-1,2-噻唑-5-基)亚甲基氨基]硫脲 N-苄基-2-氯吡咯 N-Boc-2-氨基-3-溴噻吩 N-(2-氯-4-甲基-3-噻吩)-4,5-二氢-1H-咪唑-2-胺盐酸盐 N-(2,5-二溴-1H-吡咯-1-基)-氨基甲酸叔丁酯 N,N-二甲基-5-碘-1H-吡唑-1-磺酰胺 N,N-二甲基-2-(3,4,5-三溴吡唑-1-基)丙酰胺