Triphenyl(tetradecyl)phosphonium Bromide - ≥97% , CAS No.25791-20-2

CAS: 25791-20-2 Cat. No.: T162766 Peso molecular: 539.58 Número EC: 247-267-1 PubChem CID: 3084442

GRADE & PURITY ≥97%

Synonyms

C32H44BrP | Tetradecyltriphenylphosphoniumbromide | DTXSID00948695 | T1506 | (1-Tetradecyl)triphenylphosphonium bromide | FT-0604570 | SY103615 | triphenyl(tetradecyl)phosphanium bromide | triphenyl(tetradecyl)phosphanium;bromide | J-016136 | AC9704 | n-T

Storage

Argon charged,Room temperature

Shipped In

Normal

Specifications

Sinónimos

C32H44BrP | Tetradecyltriphenylphosphoniumbromide | DTXSID00948695 | T1506 | (1-Tetradecyl)triphenylphosphonium bromide | FT-0604570 | SY103615 | triphenyl(tetradecyl)phosphanium bromide | triphenyl(tetradecyl)phosphanium;bromide | J-016136 | AC9704 | n-T

Especificaciones y pureza

≥97%

Condiciones de almacenamiento de almacenamiento

Argon charged, Room temperature

Enviado en

Normal

Pureza

≥97%

Nombres e identificadores

• Pubchem Sid: 504762435
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504762435
• Sonrisas canónicas: CCCCCCCCCCCCCC[P+](C1=CC=CC=C1)(C2=CC=CC=C2)C3=CC=CC=C3.[Br-]
• IUPAC Name: triphenyl(tetradecyl)phosphanium;bromide
• InChIKey: FUMBGFNGBMYHGH-UHFFFAOYSA-M
• INCHI: 1S/C32H44P.BrH/c1-2-3-4-5-6-7-8-9-10-11-12-22-29-33(30-23-16-13-17-24-30,31-25-18-14-19-26-31)32-27-20-15-21-28-32;/h13-21,23-28H,2-12,22,29H2,1H3;1H/q+1;/p-1
• Isómeros SMILES: CCCCCCCCCCCCCC[P+](C1=CC=CC=C1)(C2=CC=CC=C2)C3=CC=CC=C3.[Br-]
• PubChem CID: 3084442
• Peso molecular: 539.58
• Reaxy-Rn: 3582243

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: Organophosphorus compounds Organic bromide salts Hydrocarbon derivatives Organic cations
• Molecular Framework: Aromatic homomonocyclic compounds
• Substituents: Triphenylphosphine - Phenylphosphine - Hydrocarbon derivative - Organic bromide salt - Organic salt - Organophosphorus compound - Organic cation - 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

• Solubilidad: Slightly soluble in Water.94 °C
• Sensibilidad: Moisture sensitive.
• Punto de fusión (°C): 94 °C
• Peso molecular: 539.600 g/mol
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 16
• Exact Mass: 538.236 Da
• Monoisotopic Mass: 538.236 Da
• Topological Polar Surface Area: 0.000 Ų
• Heavy Atom Count: 34
• Formal Charge: 0
• Complexity: 408.000
• 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. Wencheng Zhong, Ximeng Wang, Xiaobin Yi, Lin Wang, Tinghuan Yang, Tianqi Niu, Junqin Shi, Kui Zhao, Li Shang.  (2025)  Nanoconfined Microenvironment-Regulated Photochromic Kinetics in Gold Nanocluster-Based Photoswitching Fluorescent Nanoparticles.  ACS Nano,      [PMID:40782087] [10.1021/acsnano.5c10175]