Tris(pentafluorophenyl)phosphine - ≥95% , CAS No.1259-35-4

CAS: 1259-35-4 Cat. No.: T115586 Formula: C₁₈F₁₅P Peso molecolare: 532.14 Beilstein Registry Number: 773243 Numero EC: 215-021-2 PubChem CID: 102076

GRADE & PURITY ≥95%

Synonyms

AS-66527 | T2484 | Tris(2,3,4,5,6-pentafluorophenyl)phosphine # | Tris(2,3,4,5,6-pentafluorophenyl)phosphine | UNII-R4P6L83YFZ | EINECS 215-021-2 | D70445 | A805443 | Tris(pentafluorophenyl)phosphine | A818524 | FT-0652908 | C18F15P | HY-W008896 | SY00984

Storage

Room temperature,Argon charged

Shipped In

Normal

Specifications

Sinonimi

AS-66527 | T2484 | Tris(2,3,4,5,6-pentafluorophenyl)phosphine # | Tris(2,3,4,5,6-pentafluorophenyl)phosphine | UNII-R4P6L83YFZ | EINECS 215-021-2 | D70445 | A805443 | Tris(pentafluorophenyl)phosphine | A818524 | FT-0652908 | C18F15P | HY-W008896 | SY00984

Specifiche e purezza

≥95%

Condizioni di conservazione di stoccaggio

Room temperature,Argon charged

Spedito in

Normal

Purezza

≥95%

Nomi e identificatori

• Pubchem Sid: 504756506
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504756506
• Sorrisi canonici: C1(=C(C(=C(C(=C1F)F)P(C2=C(C(=C(C(=C2F)F)F)F)F)C3=C(C(=C(C(=C3F)F)F)F)F)F)F)F
• IUPAC Name: tris(2,3,4,5,6-pentafluorophenyl)phosphane
• InChIKey: FQLSDFNKTNBQLC-UHFFFAOYSA-N
• INCHI: 1S/C18F15P/c19-1-4(22)10(28)16(11(29)5(1)23)34(17-12(30)6(24)2(20)7(25)13(17)31)18-14(32)8(26)3(21)9(27)15(18)33
• Isomeri SMILES: C1(=C(C(=C(C(=C1F)F)P(C2=C(C(=C(C(=C2F)F)F)F)F)C3=C(C(=C(C(=C3F)F)F)F)F)F)F)F
• WGK Germania: 3
• PubChem CID: 102076
• Peso molecolare: 532.14
• Beilstein: 773243
• Reaxy-Rn: 773243

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Classe Benzene and substituted derivatives
      • Subclass Phenylphosphines and derivatives

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Classe: Benzene and substituted derivatives
• Subclass: Phenylphosphines and derivatives
• Intermediate Tree Nodes: Not available
• Direct Parent: Phenylphosphines and derivatives
• Alternative Parents: Fluorobenzenes Aryl fluorides Organic phosphines and derivatives Organopnictogen compounds Organofluorides Hydrocarbon derivatives
• Molecular Framework: Aromatic homomonocyclic compounds
• Substituents: Triphenylphosphine - Phenylphosphine - Halobenzene - Fluorobenzene - Aryl halide - Aryl fluoride - Phosphine - Organopnictogen compound - Hydrocarbon derivative - Organophosphorus compound - Organofluoride - Organohalogen compound - Aromatic homomonocyclic compound
• Descrizione: This compound belongs to the class of organic compounds known as phenylphosphines and derivatives. These are compounds containing a phenylphosphine, which consists of phosphine substituent bound to a phenyl group.
• 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

Proprietà chimiche e fisiche

• Punto di fusione (°C): 108-110°C
• Peso molecolare: 532.100 g/mol
• XLogP3: 6.100
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 15
• Rotatable Bond Count: 3
• Exact Mass: 531.95 Da
• Monoisotopic Mass: 531.95 Da
• Topological Polar Surface Area: 0.000 Ų
• Heavy Atom Count: 34
• Formal Charge: 0
• Complexity: 566.000
• 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

Riferimenti

1. Dongchun Chen, Mingyao Hong, Jianglong Wan, Weishan Li, Youhao Liao.  (2024)  TPFPP@PMMA core-shell polymer modified flame retardant separator achieved by aqueous technique for high-voltage lithium metal batteries.  REACTIVE & FUNCTIONAL POLYMERS,      [PMID:] [10.1016/j.reactfunctpolym.2024.106130]