Tetraphenylphosphonium Iodide - ≥98% , CAS No.2065-67-0

CAS: 2065-67-0 Cat. No.: T162772 Peso molecular: 466.3 Beilstein Registry Number: 16(4)1013 Número EC: 218-179-0 PubChem CID: 2724164

GRADE & PURITY ≥98%

Synonyms

T1450 | ?TETRAPHENYLPHOSPHONIUM IODIDE | Tetraphenylphosphonium iodide | Tetraphenylphosphoniumiodide | A814787 | J-013501 | FT-0634015 | AKOS015833279 | AC8939 | SCHEMBL158514 | tetraphenylphosphanium;iodide | DTXSID60942851 | EINECS 218-179-0 | tetraphe

Storage

Protected from light,Argon charged,Room temperature

Shipped In

Normal

Specifications

Sinónimos

T1450 | ?TETRAPHENYLPHOSPHONIUM IODIDE | Tetraphenylphosphonium iodide | Tetraphenylphosphoniumiodide | A814787 | J-013501 | FT-0634015 | AKOS015833279 | AC8939 | SCHEMBL158514 | tetraphenylphosphanium;iodide | DTXSID60942851 | EINECS 218-179-0 | tetraphe

Especificaciones y pureza

≥98%

Condiciones de almacenamiento de almacenamiento

Protected from light, Argon charged, Room temperature

Enviado en

Normal

Pureza

≥98%

Nombres e identificadores

• Pubchem Sid: 488192252
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488192252
• Sonrisas canónicas: C1=CC=C(C=C1)[P+](C2=CC=CC=C2)(C3=CC=CC=C3)C4=CC=CC=C4.[I-]
• IUPAC Name: tetraphenylphosphanium;iodide
• InChIKey: AEFPPQGZJFTXDR-UHFFFAOYSA-M
• INCHI: 1S/C24H20P.HI/c1-5-13-21(14-6-1)25(22-15-7-2-8-16-22,23-17-9-3-10-18-23)24-19-11-4-12-20-24;/h1-20H;1H/q+1;/p-1
• Isómeros SMILES: C1=CC=C(C=C1)[P+](C2=CC=CC=C2)(C3=CC=CC=C3)C4=CC=CC=C4.[I-]
• PubChem CID: 2724164
• Peso molecular: 466.3
• Beilstein: 16(4)1013
• Reaxy-Rn: 3922216

Taxonomic Classification

Taxonomy Tree

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

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Clase: Benzene and substituted derivatives
• Subclass: Phenylphosphines and derivatives
• Intermediate Tree Nodes: Not available
• Direct Parent: Phenylphosphines and derivatives
• Alternative Parents: Organopnictogen compounds Organophosphorus compounds Organic iodide salts Hydrocarbon derivatives
• Molecular Framework: Aromatic homomonocyclic compounds
• Substituents: Triphenylphosphine - Phenylphosphine - Organopnictogen compound - Hydrocarbon derivative - Organic iodide salt - Organic salt - Organophosphorus compound - Aromatic homomonocyclic compound
• Descripción: 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

Propiedades químicas y físicas

• Sensibilidad: Light Sensitive，Moisture sensitive
• Punto de fusión (°C): 345-350℃
• Peso molecular: 466.300 g/mol
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 4
• Exact Mass: 466.035 Da
• Monoisotopic Mass: 466.035 Da
• Topological Polar Surface Area: 0.000 Ų
• Heavy Atom Count: 26
• Formal Charge: 0
• Complexity: 301.000
• 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: 2

XLogP3

Referencias

1. Yongqiang Zhou, Zixian Wang, linfeng Guo, Lei Huang, Yichen Liu, Mengyue Wu, Qian Zhang, Kang An, Peng He, Fei Wang, Juan Du, Zhengzheng Liu, Zhiping Hu, Yuxin Leng, Yayun Pu, Jun’an Lai, Xiaosheng Tang.  (2024)  Ultrafast and high-resolution X-ray imaging based on zero-dimensional organic silver halides.  Materials Chemistry Frontiers,      [PMID:] [10.1039/D4QM00362D]