5-Ethoxymethylfurfural - ≥97% , CAS No.1917-65-3

CAS: 1917-65-3 Cat. No.: E133055 Peso molecular: 154.16 Número EC: 803-242-2

GRADE & PURITY ≥97%

Synonyms

MFCD06803262 | W-200195 | EN300-130494 | CCDRPZFMDMKZSZ-UHFFFAOYSA-N | GEO-02730 | Q27236349 | Z1198171016 | AS-64475 | ethoxymethylfurfural | 0826YO734G | 5-(Ethoxymethyl)furfural | SB61106 | BB 0220435 | UNII-0826YO734G | EMF | SCHEMBL273028 | 5-(Ethoxy

Storage

Store at 2-8°C,Argon charged

Shipped In

Wet ice

Specifications

Sinónimos

MFCD06803262 | W-200195 | EN300-130494 | CCDRPZFMDMKZSZ-UHFFFAOYSA-N | GEO-02730 | Q27236349 | Z1198171016 | AS-64475 | ethoxymethylfurfural | 0826YO734G | 5-(Ethoxymethyl)furfural | SB61106 | BB 0220435 | UNII-0826YO734G | EMF | SCHEMBL273028 | 5-(Ethoxy

Especificaciones y pureza

≥97%

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

≥97%

Nombres e identificadores

• Pubchem Sid: 504767189
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504767189
• Sonrisas canónicas: CCOCC1=CC=C(O1)C=O
• IUPAC Name: 5-(ethoxymethyl)furan-2-carbaldehyde
• InChIKey: CCDRPZFMDMKZSZ-UHFFFAOYSA-N
• INCHI: 1S/C8H10O3/c1-2-10-6-8-4-3-7(5-9)11-8/h3-5H,2,6H2,1H3
• Isómeros SMILES: CCOCC1=CC=C(O1)C=O
• WGK Alemania: 3
• Peso molecular: 154.16
• Reaxy-Rn: 137823
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=137823&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic oxygen compounds
    • Clase Organooxygen compounds
      • Subclass Carbonyl compounds
        • Level5 Aldehydes
          • Level6 Aryl-aldehydes

• Kingdom: Organic compounds
• Superclass: Organic oxygen compounds
• Clase: Organooxygen compounds
• Subclass: Carbonyl compounds
• Intermediate Tree Nodes: Aldehydes
• Direct Parent: Aryl-aldehydes
• Alternative Parents: Heteroaromatic compounds Furans Oxacyclic compounds Dialkyl ethers Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aromatic heteromonocyclic compounds
• Substituents: Aryl-aldehyde - Heteroaromatic compound - Furan - Oxacycle - Organoheterocyclic compound - Ether - Dialkyl ether - Organic oxide - Hydrocarbon derivative - Aromatic heteromonocyclic compound
• Descripción: This compound belongs to the class of organic compounds known as aryl-aldehydes. These are compounds containing an aldehyde group directly attached to an aromatic ring.
• 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

• Índice de refracción: 1.511
• Punto de inflamación (°F): >230 °F
• Punto de inflamación (°C): >110 °C
• Punto de ebullición (°C): 267-274 °C/760 mmHg
• Peso molecular: 154.160 g/mol
• XLogP3: 0.300
• 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: 39.400 Ų
• Heavy Atom Count: 11
• Formal Charge: 0
• Complexity: 125.000
• 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. Lincai Peng, Chaonan Tao, Hui Yang, Junhua Zhang, Huai Liu.  (2022)  Mechanistic insights into the effect of the feed concentration on product formation during acid-catalyzed conversion of glucose in ethanol.  GREEN CHEMISTRY,  24  (13): (5219-5227).  [PMID:] [10.1039/D2GC00300G]

2. Xin Yu, Lincai Peng, Jun Dai, Hui Li, Chaonan Tao, Fa Yang, Junhua Zhang.  (2021)  Ethylene glycol co-solvent enhances alkyl levulinate production from concentrated feeds of sugars in monohydric alcohols.  FUEL,      [PMID:] [10.1016/j.fuel.2021.121471]

3. Hualei Hu, Tingting Xue, Zhenxin Zhang, Jiang Gan, Liangqi Chen, Jian Zhang, Fengzuo Qu, Weijie Cai, Lei Wang.  (2021)  Direct Conversion of 5-Hydroxymethylfurfural to Furanic Diether by Copper-Loaded Hierarchically Structured ZSM-5 Catalyst in a Fixed-Bed Reactor.  ChemCatChem,  13  (15): (3461-3469).  [PMID:] [10.1002/cctc.202100489]

4. Chaonan Tao, Lincai Peng, Junhua Zhang, Liang He.  (2020)  Al-modified heteropolyacid facilitates alkyl levulinate production from cellulose and lignocellulosic biomass: Kinetics and mechanism studies.  FUEL PROCESSING TECHNOLOGY,      [PMID:] [10.1016/j.fuproc.2020.106709]

5. Danxin Hu, Hualei Hu, Haitao Jin, Pilan Zhang, Yunhan Hu, Suhua Ying, Xianming Li, Yong Yang, Jian Zhang, Lei Wang.  (2019)  Building hierarchical zeolite structure by post-synthesis treatment to promote the conversion of furanic molecules into biofuels.  APPLIED CATALYSIS A-GENERAL,      [PMID:] [10.1016/j.apcata.2019.117338]

6. Jinlong Li, Yuqi Wang, Boqiong Lu, Yingxiong Wang, Tiansheng Deng, Xianglin Hou.  (2018)  Protonic acid catalysis of sulfonated carbon material: Tunable and selective conversion of fructose in low-boiling point solvent.  APPLIED CATALYSIS A-GENERAL,      [PMID:] [10.1016/j.apcata.2018.08.027]

7. Niakan Mahsa, Qian Chao, Zhou Shaodong.  (2025)  High-efficiency synthesis of 5‑ethoxymethylfurfural from biomass-derived 5-hydroxymethylfurfural and sugars catalyzed by magnetically recoverable hydrogen sulfate ionic liquid.  Biomass Conversion and Biorefinery,      [PMID:] [10.1007/s13399-025-06609-2]

8. Huai Liu, Yanping Kong, Weipeng Song, Rui Zhang, Junhua Zhang, Yong Sun, Lincai Peng.  (2024)  Pretreatment greatly facilitates ethyl levulinate production from catalytic alcoholysis of Napier grass stem.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2024.148559]

9. Zilong Rao, Yu Zhang, Shuailong Zhao, Huai Liu, Rui Zhang, Wenlong Jia, Junhua Zhang, Yong Sun, Lincai Peng.  (2025)  Rational Improvement for the Catalytic Alcoholysis of Straw Biomass by Understanding the Role of Inorganic Components.  ACS Sustainable Chemistry & Engineering,      [PMID:] [10.1021/acssuschemeng.5c00690]