Furfuryl glycidyl ether - ≥96% , CAS No.5380-87-0

CAS: 5380-87-0 Cat. No.: H111929 Peso molecular: 154.16 Número EC: 226-372-6

GRADE & PURITY ≥96%

Synonyms

2-((oxiran-2-ylmethoxy)methyl)furan | Drotebanol (INN) | DTXSID90968589 | 2-((Oxiranylmethoxy)methyl)furan | 2,3-Epoxypropyl-furfurylether | 2-[(2-Oxiranylmethoxy)methyl]furan | 2-oxiranylmethoxymethyl-furan | Furan, 2-((2,3-epoxypropoxy)methyl)- | MFCD00

Storage

Store at 2-8°C,Protected from light,Argon charged

Shipped In

Wet ice

Specifications

Sinónimos

2-((oxiran-2-ylmethoxy)methyl)furan | Drotebanol (INN) | DTXSID90968589 | 2-((Oxiranylmethoxy)methyl)furan | 2, 3-Epoxypropyl-furfurylether | 2-[(2-Oxiranylmethoxy)methyl]furan | 2-oxiranylmethoxymethyl-furan | Furan, 2-((2, 3-epoxypropoxy)methyl)- | MFCD00

Especificaciones y pureza

≥96%

Condiciones de almacenamiento de almacenamiento

Store at 2-8°C, Protected from light, Argon charged

Enviado en

Wet ice

Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.

Pureza

≥96%

Nombres e identificadores

• Pubchem Sid: 504756211
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504756211
• Sonrisas canónicas: C1C(O1)COCC2=CC=CO2
• IUPAC Name: 2-(oxiran-2-ylmethoxymethyl)furan
• InChIKey: RUGWIVARLJMKDM-UHFFFAOYSA-N
• INCHI: 1S/C8H10O3/c1-2-7(10-3-1)4-9-5-8-6-11-8/h1-3,8H,4-6H2
• Isómeros SMILES: C1C(O1)COCC2=CC=CO2
• WGK Alemania: 3
• Peso molecular: 154.16
• Reaxy-Rn: 1239147
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1239147&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organoheterocyclic compounds
    • Clase Heteroaromatic compounds

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Clase: Heteroaromatic compounds
• Subclass: Not available
• Intermediate Tree Nodes: Not available
• Direct Parent: Heteroaromatic compounds
• Alternative Parents: Furans Oxacyclic compounds Epoxides Dialkyl ethers Hydrocarbon derivatives
• Molecular Framework: Aromatic heteromonocyclic compounds
• Substituents: Heteroaromatic compound - Furan - Oxacycle - Ether - Oxirane - Dialkyl ether - Organic oxygen compound - Hydrocarbon derivative - Organooxygen compound - Aromatic heteromonocyclic compound
• Descripción: This compound belongs to the class of organic compounds known as heteroaromatic compounds. These are compounds containing an aromatic ring where a carbon atom is linked to an hetero atom.
• External Descriptors: Not available

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Propiedades químicas y físicas

• Sensibilidad: air sensitive;light sensitive;heat sensitive
• Índice de refracción: 1.481
• Punto de inflamación (°F): 102°C
• Punto de inflamación (°C): 102°C
• Punto de ebullición (°C): 103-104 °C/11 mmHg
• Peso molecular: 154.160 g/mol
• XLogP3: 0.400
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 4
• Exact Mass: 154.063 Da
• Monoisotopic Mass: 154.063 Da
• Topological Polar Surface Area: 34.900 Ų
• Heavy Atom Count: 11
• Formal Charge: 0
• Complexity: 127.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 1
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1

Referencias

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2. Ying Li, Bo Jiang, Yudong Huang.  (2022)  Interfacial self-healing performance of carbon fiber/epoxy based on postsynthetic modification of metal-organic frameworks.  COMPOSITES SCIENCE AND TECHNOLOGY,      [PMID:] [10.1016/j.compscitech.2022.109564]

3. Yuting Zou, Lingyu Li, Bin Tan, Yue Ma, Liang Fang, Chunhua Lu, Zhongzi Xu.  (2019)  Silane modified epoxy coatings with low surface tension to achieve self-healing of wide damages.  PROGRESS IN ORGANIC COATINGS,      [PMID:] [10.1016/j.porgcoat.2019.04.065]

4. Tao Zhang, Ruijia Wang, Wei Li, Shujun Li, Bing Tian, Shouxin Liu, Zhijun Chen.  (2025)  A metal-, solvent-, halogen-, and additive-free catalysis for CO2 fixation by carbon dots.  Journal of Materials Chemistry A,      [PMID:] [10.1039/D4TA08934K]

5. Jinsong Wang, Farzad Seidi, Xiaotong Shi, Chengcheng Li, Yang Huang, Huining Xiao.  (2024)  Lignin self-healing coatings based on thermo-reversible Diels-Alder reaction for anticorrosion applications.  PROGRESS IN ORGANIC COATINGS,      [PMID:] [10.1016/j.porgcoat.2024.108428]

6. Jinsong Wang, Farzad Seidi, Xiaotong Shi, Chengcheng Li, Yang Huang, Huining Xiao.  (2024)  Unveiling the potential of dual-extrinsic/intrinsic self-healing lignin-based coatings for anticorrosion applications.  INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES,      [PMID:39617231] [10.1016/j.ijbiomac.2024.138073]

7. Zhou Jie, Yu Wen-Wang, Meng Xiang-Guang, Li Wen, Chu Dan-Dan.  (2025)  Imidazolium-Based Deep Eutectic Solvents Catalyzed Cycloaddition Reaction of Epoxide with CO2 in Simulated Flue Gas.  CATALYSIS LETTERS,  155  (10): (1-11).  [PMID:] [10.1007/s10562-025-05174-7]

8. Haoran Xu, Shunli Wang, Kaijing Hu, Haixu Dou, Pengpeng Lu, Jianfu Wang, Yinsheng Li, Huichao Jin, Limei Tian, Luquan Ren.  (2025)  Bioinspired mechanically tough, high Adhesion, and healable polyurethane coating for high-temperature anti-corrosion and anti-cavitation applications.  APPLIED SURFACE SCIENCE,      [PMID:] [10.1016/j.apsusc.2025.163584]

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