Diethylphenylphosphine - ≥97% , CAS No.1605-53-4

CAS: 1605-53-4 Cat. No.: D154321 Peso molecular: 166.2 Beilstein Registry Number: 742484 Número EC: 216-516-6

GRADE & PURITY ≥97%

Synonyms

AS-58641 | SCHEMBL231466 | AKOS015839009 | NSC 158475 | diethyl(phenyl)phosphine | J-009733 | diethyl(phenyl)phosphane | Diethylphenylphosphine, 96% | FT-0624799 | NSC158475 | NSC-158475 | MFCD00015172 | DTXSID40166891 | A883198 | Diethylphenylphosphene |

Storage

Argon charged,Room temperature

Shipped In

Normal

Descripción general

Catalyst for: . Selective cross-dimerization . Diastereoselective condensations . Carboxyl migration reactions . Selective hydrogenation . Asymmetric induction by chiral diphosphines in ring contraction

Specifications

Sinónimos

AS-58641 | SCHEMBL231466 | AKOS015839009 | NSC 158475 | diethyl(phenyl)phosphine | J-009733 | diethyl(phenyl)phosphane | Diethylphenylphosphine, 96% | FT-0624799 | NSC158475 | NSC-158475 | MFCD00015172 | DTXSID40166891 | A883198 | Diethylphenylphosphene |

Especificaciones y pureza

≥97%

Condiciones de almacenamiento de almacenamiento

Argon charged, Room temperature

Enviado en

Normal

Pureza

≥97%

Nombres e identificadores

• Pubchem Sid: 488184876
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488184876
• Sonrisas canónicas: CCP(CC)C1=CC=CC=C1
• IUPAC Name: diethyl(phenyl)phosphane
• InChIKey: LVTCZSBUROAWTE-UHFFFAOYSA-N
• INCHI: 1S/C10H15P/c1-3-11(4-2)10-8-6-5-7-9-10/h5-9H,3-4H2,1-2H3
• Isómeros SMILES: CCP(CC)C1=CC=CC=C1
• WGK Alemania: 3
• Peso molecular: 166.2
• Beilstein: 742484
• Reaxy-Rn: 742484
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=742484&ln=

Taxonomic Classification

Taxonomy Tree

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

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Clase: Benzene and substituted derivatives
• Subclass: Not available
• Intermediate Tree Nodes: Not available
• Direct Parent: Benzene and substituted derivatives
• Alternative Parents: Organic phosphines and derivatives Organopnictogen compounds Hydrocarbon derivatives
• Molecular Framework: Aromatic homomonocyclic compounds
• Substituents: Monocyclic benzene moiety - Phosphine - Organopnictogen compound - Hydrocarbon derivative - Organophosphorus compound - Aromatic homomonocyclic compound
• Descripción: This compound belongs to the class of organic compounds known as benzene and substituted derivatives. These are aromatic compounds containing one monocyclic ring system consisting of benzene.
• 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: air sensitive;Moisture sensitive
• Índice de refracción: 1.55
• Punto de inflamación (°F): 183.2 °F
• Punto de inflamación (°C): 84 °C
• Punto de ebullición (°C): 220 °C
• Peso molecular: 166.200 g/mol
• XLogP3: 2.200
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 0
• Rotatable Bond Count: 3
• Exact Mass: 166.091 Da
• Monoisotopic Mass: 166.091 Da
• Topological Polar Surface Area: 0.000 Ų
• Heavy Atom Count: 11
• Formal Charge: 0
• Complexity: 91.000
• 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

Referencias

1. Xinrong Li, Shuliang Chen, Peng Yang, Yue Lin, Chen Chen, Xianzhi Hu, Futing Zi.  (2024)  Effective and selective recovery of Au(III) from WPCBs using quaternary phosphonium adsorbent synthesized by adjusting steric hindrance.  JOURNAL OF HAZARDOUS MATERIALS,      [PMID:38878433] [10.1016/j.jhazmat.2024.134881]