Isobutyltriphenylphosphonium bromide - ≥98% , CAS No.22884-29-3

CAS: 22884-29-3 Cat. No.: I189083 Peso molecular: 399.31 Número EC: 245-291-7

GRADE & PURITY ≥98%

Synonyms

AKOS015900341 | SY106402 | FT-0627347 | Phosphonium, (2-methylpropyl)triphenyl-, bromide | F17182 | (2-Methylpropyl)triphenylphosphonium bromide | 2-methylpropyl(triphenyl)phosphanium;bromide | FT-0627377 | MFCD00031593 | BB 0322389 | VIKPDPHNYHUZQW-UHFFF

Storage

Room temperature

Shipped In

Normal

Specifications

Sinónimos

AKOS015900341 | SY106402 | FT-0627347 | Phosphonium, (2-methylpropyl)triphenyl-, bromide | F17182 | (2-Methylpropyl)triphenylphosphonium bromide | 2-methylpropyl(triphenyl)phosphanium;bromide | FT-0627377 | MFCD00031593 | BB 0322389 | VIKPDPHNYHUZQW-UHFFF

Especificaciones y pureza

≥98%

Condiciones de almacenamiento de almacenamiento

Room temperature

Enviado en

Normal

Pureza

≥98%

Nombres e identificadores

• Pubchem Sid: 488192285
• Sonrisas canónicas: CC(C)C[P+](C1=CC=CC=C1)(C2=CC=CC=C2)C3=CC=CC=C3.[Br-]
• IUPAC Name: 2-methylpropyl(triphenyl)phosphanium;bromide
• InChIKey: VIKPDPHNYHUZQW-UHFFFAOYSA-M
• INCHI: 1S/C22H24P.BrH/c1-19(2)18-23(20-12-6-3-7-13-20,21-14-8-4-9-15-21)22-16-10-5-11-17-22;/h3-17,19H,18H2,1-2H3;1H/q+1;/p-1
• Isómeros SMILES: CC(C)C[P+](C1=CC=CC=C1)(C2=CC=CC=C2)C3=CC=CC=C3.[Br-]
• Peso molecular: 399.31
• Reaxy-Rn: 4171228
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=4171228&ln=

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 bromide salts Hydrocarbon derivatives
• Molecular Framework: Aromatic homomonocyclic compounds
• Substituents: Triphenylphosphine - Phenylphosphine - Organopnictogen compound - Hydrocarbon derivative - Organic bromide 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

• Punto de fusión (°C): 198-202℃
• Peso molecular: 399.300 g/mol
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 5
• Exact Mass: 398.08 Da
• Monoisotopic Mass: 398.08 Da
• Topological Polar Surface Area: 0.000 Ų
• Heavy Atom Count: 24
• Formal Charge: 0
• Complexity: 284.000
• 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. Juexin Huang, Jingyi Xia, Sravan Baddi, Yu Zhao, Chuan-liang Feng.  (2025)  Dual-Scale Polarization Engineering of d-Phenylalanine-Based Assemblies for High-Performance Nanogenerators.  ACS Nano,      [PMID:40598888] [10.1021/acsnano.5c03436]