Furfuryl methacrylate - ≥95%, contains 200 ppm monomethyl ether hydroquinone as inhibitor , CAS No.3454-28-2

CAS: 3454-28-2 Cat. No.: F117381 Peso molecular: 166.17 Beilstein Registry Number: 17(3/4)1248 Número EC: 222-383-5

GRADE & PURITY ≥95%, contains 200 ppm monomethyl ether hydroquinone as inhibitor

Synonyms

J-019643 | NSC61377 | MFCD00134680 | Q94ZA4KCV7 | MFCD00002511 | M1335 | FT-0634863 | AKOS022182945 | m-Xylene, 4-bromo- | 2-Propenoic acid, 2-methyl-, 2-furanylmethyl ester | Furfuryl Methacrylate, (stabilized with MEHQ) | SCHEMBL36525 | (furan-2-yl)meth

Storage

Protected from light,Store at -20°C

Shipped In

Ice chest + Ice pads

Specifications

Sinónimos

J-019643 | NSC61377 | MFCD00134680 | Q94ZA4KCV7 | MFCD00002511 | M1335 | FT-0634863 | AKOS022182945 | m-Xylene, 4-bromo- | 2-Propenoic acid, 2-methyl-, 2-furanylmethyl ester | Furfuryl Methacrylate, (stabilized with MEHQ) | SCHEMBL36525 | (furan-2-yl)meth

Especificaciones y pureza

≥95%, contains 200 ppm monomethyl ether hydroquinone as inhibitor

Condiciones de almacenamiento de almacenamiento

Protected from light, Store at -20°C

Enviado en

Ice chest + Ice pads

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

Pureza

≥95%

Nombres e identificadores

• Sonrisas canónicas: CC(=C)C(=O)OCC1=CC=CO1
• IUPAC Name: furan-2-ylmethyl 2-methylprop-2-enoate
• InChIKey: DWXAVNJYFLGAEF-UHFFFAOYSA-N
• INCHI: 1S/C9H10O3/c1-7(2)9(10)12-6-8-4-3-5-11-8/h3-5H,1,6H2,2H3
• Isómeros SMILES: CC(=C)C(=O)OCC1=CC=CO1
• WGK Alemania: 3
• Peso molecular: 166.17
• Beilstein: 17(3/4)1248
• Reaxy-Rn: 124519
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=124519&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 Enoate esters Oxacyclic compounds Monocarboxylic acids and derivatives Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aromatic heteromonocyclic compounds
• Substituents: Heteroaromatic compound - Alpha,beta-unsaturated carboxylic ester - Enoate ester - Furan - Carboxylic acid ester - Oxacycle - Monocarboxylic acid or derivatives - Carboxylic acid derivative - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - 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: Light sensitive
• Índice de refracción: 1.48
• Punto de inflamación (°F): 195.8 °F
• Punto de inflamación (°C): 91 °C
• Punto de ebullición (°C): 82 °C/5 mmHg
• Peso molecular: 166.170 g/mol
• XLogP3: 1.700
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 4
• Exact Mass: 166.063 Da
• Monoisotopic Mass: 166.063 Da
• Topological Polar Surface Area: 39.400 Ų
• Heavy Atom Count: 12
• Formal Charge: 0
• Complexity: 186.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• 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. Tong Luo, Chuanwei Lu, Ji Qi, Chunpeng Wang, Fuxiang Chu, Jifu Wang.  (2023)  Fabrication of well-defined lignin-derived elastomers by atom transfer radical polymerization and Diels-Alder reaction towards sustainable, super-tough and high temperature-resistant hot-melt adhesives.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2023.147729]

2. Yangjing Chen, Zhiyu Hu, Hongting Pu.  (2023)  Macromolecular Metamorphosis in a Polymer Network via the Reversible Collapse of Single-Chain Nanoparticles.  MACROMOLECULES,      [PMID:] [10.1021/acs.macromol.3c01627]

3. Y. You, M.R. Fu, M.Z. Rong, M.Q. Zhang.  (2021)  Improving creep resistance while maintaining reversibility of covalent adaptive networks via constructing reversibly interlocked polymer networks.  Materials Today Chemistry,      [PMID:] [10.1016/j.mtchem.2021.100687]

4. Chuanwei Lu, Xiaoliang Guo, Chunpeng Wang, Jifu Wang, Fuxiang Chu.  (2020)  Integration of metal-free ATRP and Diels-Alder reaction toward sustainable and recyclable cellulose-based thermoset elastomers.  CARBOHYDRATE POLYMERS,      [PMID:32564832] [10.1016/j.carbpol.2020.116404]