4-Vinyl-1-cyclohexene-1,2-epoxide - ≥98%, mixture of isomers , CAS No.106-86-5

CAS: 106-86-5 Cat. No.: V102412 Fórmula: C₈H₁₂O Peso molecular: 124.18 Número EC: 203-436-1 PubChem CID: 7832

GRADE & PURITY ≥98%, mixture of isomers

Synonyms

1-Vinyl-3,4-epoxycyclohexane | 3-Vinyl-7-oxabicyclo(4.1.0)heptane | NSC35409 | NSC-35409 | 4-Vinylcyclohexene-1,2-epoxide | 3-Vinyl-7-oxabicyclo[4.1.0]heptane | AI3-26045 | EP-101 | NSC 35409 | EINECS 203-436-1 | WLN: T36 BOTJ E1U1 | 7-Oxabicyclo[4.1.0]he

Storage

Store at 2-8°C,Argon charged

Shipped In

Wet ice

Specifications

Sinónimos

1-Vinyl-3,4-epoxycyclohexane | 3-Vinyl-7-oxabicyclo(4.1.0)heptane | NSC35409 | NSC-35409 | 4-Vinylcyclohexene-1,2-epoxide | 3-Vinyl-7-oxabicyclo[4.1.0]heptane | AI3-26045 | EP-101 | NSC 35409 | EINECS 203-436-1 | WLN: T36 BOTJ E1U1 | 7-Oxabicyclo[4.1.0]he

Especificaciones y pureza

≥98%, mixture of isomers

Condiciones de almacenamiento de almacenamiento

Store at 2-8°C,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

≥98%

Nombres e identificadores

• Pubchem Sid: 504751478
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504751478
• Sonrisas canónicas: C=CC1CCC2C(C1)O2
• IUPAC Name: 3-ethenyl-7-oxabicyclo[4.1.0]heptane
• InChIKey: SLJFKNONPLNAPF-UHFFFAOYSA-N
• INCHI: 1S/C8H12O/c1-2-6-3-4-7-8(5-6)9-7/h2,6-8H,1,3-5H2
• Isómeros SMILES: C=CC1CCC2C(C1)O2
• WGK Alemania: 3
• RTECS: RN8770000
• PubChem CID: 7832
• Número ONU: 3271
• Peso molecular: 124.18
• Reaxy-Rn: 107390

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organoheterocyclic compounds
    • Clase Oxepanes

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Clase: Oxepanes
• Subclass: Not available
• Intermediate Tree Nodes: Not available
• Direct Parent: Oxepanes
• Alternative Parents: Oxacyclic compounds Epoxides Dialkyl ethers Hydrocarbon derivatives
• Molecular Framework: Aliphatic heteropolycyclic compounds
• Substituents: Oxepane - Oxacycle - Ether - Oxirane - Dialkyl ether - Organic oxygen compound - Hydrocarbon derivative - Organooxygen compound - Aliphatic heteropolycyclic compound
• Descripción: This compound belongs to the class of organic compounds known as oxepanes. These are compounds containing an oxepane ring, which is a seven-member saturated aliphatic heterocycle with one oxygen and six carbon atoms.
• 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

• Solubilidad: Insoluble in water.
• Sensibilidad: Heat sensitive；air sensitive
• Índice de refracción: 1.469
• Punto de inflamación (°F): 46 °C
• Punto de inflamación (°C): 46°C
• Punto de ebullición (°C): 169°C
• Punto de fusión (°C): -100°C(lit.)
• Peso molecular: 124.180 g/mol
• XLogP3: 1.700
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 1
• Exact Mass: 124.089 Da
• Monoisotopic Mass: 124.089 Da
• Topological Polar Surface Area: 12.500 Ų
• Heavy Atom Count: 9
• Formal Charge: 0
• Complexity: 131.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 3
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1

Referencias

1. Jin Xie, Yunlang Hu, Yanjing Gao, Fang Sun.  (2023)  Synthesis and properties of trifluoromethyl organosilicon cycloaliphatic epoxy monomers for cationic photopolymerization.  JOURNAL OF APPLIED POLYMER SCIENCE,  140  (26): (e53987).  [PMID:] [10.1002/app.53987]

2. Haizhi Dou, Yunlang Hu, Yanjing Gao, Fang Sun.  (2022)  Design, synthesis and properties of trifluoromethyl polysiloxane oxetane monomers.  EUROPEAN POLYMER JOURNAL,      [PMID:] [10.1016/j.eurpolymj.2022.111756]

3. Yao Chen, Wenchuan Wang, Dong Xie, Lili Wu, Chaocan Zhang.  (2021)  Synthesis of CO2-based functional poly(carbonate-co-lactide).  JOURNAL OF POLYMER SCIENCE,  59  (14): (1528-1539).  [PMID:] [10.1002/pol.20210130]

4. Yangyang Zong, Dayong Gui, Kangmin Niu.  (2024)  Enhanced thermal and electrical conductivity in epoxy nanocomposites via liquid crystal-driven alignment of graphene.  Materials Today Communications,      [PMID:] [10.1016/j.mtcomm.2024.108067]

5. Chi Zhang, Zixuan Lei, Yuhong Liu.  (2025)  Epoxidized silicone modified polybenzoxazine resins with synergistic enhanced strength and toughness via tuning cross-linked bonding modes and network topologies.  EUROPEAN POLYMER JOURNAL,      [PMID:] [10.1016/j.eurpolymj.2025.114138]