GRADE & PURITY ≥96%

Synonyms

19932-27-5|3-(1h,1h,5h-octafluoropentyloxy)-1,2-epoxypropane|2-(2,2,3,3,4,4,5,5-octafluoropentoxymethyl)oxirane|Glycidyl 2,2,3,3,4,4,5,5-octafluoropentyl ether|2-{[(2,2,3,3,4,4,5,5-octafluoropentyl)oxy]methyl}oxirane|3-(1H,1H,5H-Octafluoropentyloxy)-1,2-p

Storage

Room temperature

Shipped In

Normal

Specifications

Synonyms

19932-27-5 | 3-(1h, 1h, 5h-octafluoropentyloxy)-1, 2-epoxypropane | 2-(2, 2, 3, 3, 4, 4, 5, 5-octafluoropentoxymethyl)oxirane | Glycidyl 2, 2, 3, 3, 4, 4, 5, 5-octafluoropentyl ether | 2-{[(2, 2, 3, 3, 4, 4, 5, 5-octafluoropentyl)oxy]methyl}oxirane | 3-(1H, 1H, 5H-Octafluoropentyloxy)-1, 2-p

Specifications & Purity

≥96%

Storage

Room temperature

Shipped In

Normal

Purity

≥96%

Names and Identifiers

• Pubchem Sid: 488193658
• Canonical Smiles: C1C(O1)COCC(C(C(C(F)F)(F)F)(F)F)(F)F
• IUPAC Name: 2-(2,2,3,3,4,4,5,5-octafluoropentoxymethyl)oxirane
• InChIKey: NABHRPSATHTFNS-UHFFFAOYSA-N
• INCHI: 1S/C8H8F8O2/c9-5(10)7(13,14)8(15,16)6(11,12)3-17-1-4-2-18-4/h4-5H,1-3H2
• Isomeric SMILES: C1C(O1)COCC(C(C(C(F)F)(F)F)(F)F)(F)F
• Molecular Weight: 288.14
• Reaxy-Rn: 5338310
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=5338310&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organoheterocyclic compounds
    • Class Epoxides

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Class: Epoxides
• Subclass: Not available
• Intermediate Tree Nodes: Not available
• Direct Parent: Epoxides
• Alternative Parents: Oxacyclic compounds Dialkyl ethers Organofluorides Hydrocarbon derivatives Alkyl fluorides
• Molecular Framework: Aliphatic heteromonocyclic compounds
• Substituents: Oxacycle - Ether - Oxirane - Dialkyl ether - Organic oxygen compound - Hydrocarbon derivative - Organooxygen compound - Organofluoride - Organohalogen compound - Alkyl halide - Alkyl fluoride - Aliphatic heteromonocyclic compound
• Description: This compound belongs to the class of organic compounds known as epoxides. These are compounds containing a cyclic ether with three ring atoms(one oxygen and two 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

Chemical and Physical Properties

• Molecular Weight: 288.130 g/mol
• XLogP3: 2.600
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 10
• Rotatable Bond Count: 7
• Exact Mass: 288.04 Da
• Monoisotopic Mass: 288.04 Da
• Topological Polar Surface Area: 21.800 Ų
• Heavy Atom Count: 18
• Formal Charge: 0
• Complexity: 293.000
• 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

References

1. Chenya Zhuo, Huiming Kong, Ke Yi, Chun-Wei Chi, Jiabing Zhang, Ran Chen, Haixia Wang, Caixia Wu, Yeh-Hsing Lao, Yu Tao, Mingqiang Li.  (2023)  Magnetic-Activated Nanosystem with Liver-Specific CRISPR Nonviral Vector to Achieve Spatiotemporal Liver Genome Editing as Hepatitis B Therapeutics.  ADVANCED FUNCTIONAL MATERIALS,  33  (7): (2210860).  [PMID:] [10.1002/adfm.202210860]

2. Xin Bai, Jian Nie, Siyao Cheng, Daohu Sheng, Jijun Xiao, Wei Dong.  (2024)  Biocompatible fluorinated poly(2-hydroxypropenimine)s for safe and efficient gene transfection.  COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS,      [PMID:] [10.1016/j.colsurfa.2024.135575]