Ethyl 1,1,2,2-tetrafluoroethyl ether(ETFE) - ≥97% , CAS No.512-51-6

CAS: 512-51-6 Cat. No.: E122292 Molecular Weight: 146.08 EC Number: 680-776-0

GRADE & PURITY ≥97%

Synonyms

LAIDESKHUQONBF-UHFFFAOYSA-N | ethyl 1,1,2,2-tetrafluoroethyl ether/HFE-374E | 374pcE-beta-gamma | Ethyl 1,1,2,2-tetrafluoroethyl ether | 1-Ethoxy-1,1,2,2-tetrafluoroethane | 1,1,2,2-tetrafluoroethyl ethyl ether | MFCD00069162 | 1,1,2,2-tetrafluoroethyl et

Storage

Room temperature

Shipped In

Normal

Overview

Ethyl 1,1,2,2-tetrafluoroethyl ether (ETFE) is a fluorinated linear ether that has several key properties that make it useful in batteries. First, ETFE is miscible with many polar organic solvents used in electrolyte formulations, which improves the ionic conductivity of the battery. Additionally, ETFE has a relatively low viscosity (486 mPa•s at 23 °C) and a low boiling point (58 °C), which make it a versatile diluent for low-temperature applications.

Specifications

Synonyms

LAIDESKHUQONBF-UHFFFAOYSA-N | ethyl 1, 1, 2, 2-tetrafluoroethyl ether/HFE-374E | 374pcE-beta-gamma | Ethyl 1, 1, 2, 2-tetrafluoroethyl ether | 1-Ethoxy-1, 1, 2, 2-tetrafluoroethane | 1, 1, 2, 2-tetrafluoroethyl ethyl ether | MFCD00069162 | 1, 1, 2, 2-tetrafluoroethyl et

Specifications & Purity

≥97%

Storage

Room temperature

Shipped In

Normal

Purity

≥97%

Names and Identifiers

• Pubchem Sid: 488187640
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488187640
• Canonical Smiles: CCOC(C(F)F)(F)F
• IUPAC Name: 1-ethoxy-1,1,2,2-tetrafluoroethane
• InChIKey: HBRLMDFVVMYNFH-UHFFFAOYSA-N
• INCHI: 1S/C4H6F4O/c1-2-9-4(7,8)3(5)6/h3H,2H2,1H3
• Isomeric SMILES: CCOC(C(F)F)(F)F
• Molecular Weight: 146.08
• Reaxy-Rn: 1740886
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1740886&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic oxygen compounds
    • Class Organooxygen compounds
      • Subclass Ethers

• Kingdom: Organic compounds
• Superclass: Organic oxygen compounds
• Class: Organooxygen compounds
• Subclass: Ethers
• Intermediate Tree Nodes: Not available
• Direct Parent: Dialkyl ethers
• Alternative Parents: Organofluorides Hydrocarbon derivatives Alkyl fluorides
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Dialkyl ether - Hydrocarbon derivative - Organofluoride - Organohalogen compound - Alkyl halide - Alkyl fluoride - Aliphatic acyclic compound
• Description: This compound belongs to the class of organic compounds known as dialkyl ethers. These are organic compounds containing the dialkyl ether functional group, with the formula ROR', where R and R' are alkyl groups.
• 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

Chemical and Physical Properties

• Refractive Index: 1.3
• Flash Point(°F): -15℃(-5°F)
• Flash Point(°C): -15℃(-5°F)
• Boil Point(°C): 56-58°C
• Molecular Weight: 146.080 g/mol
• XLogP3: 2.100
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 3
• Exact Mass: 146.035 Da
• Monoisotopic Mass: 146.035 Da
• Topological Polar Surface Area: 9.200 Ų
• Heavy Atom Count: 9
• Formal Charge: 0
• Complexity: 82.600
• 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