Cas no 31641-65-3 (Benzenamine,4-chloro-N-(triphenylphosphoranylidene)-)

Benzenamine,4-chloro-N-(triphenylphosphoranylidene)- is a phosphinimine derivative characterized by its robust reactivity as a nucleophile and ligand in organometallic chemistry. The compound features a chloro-substituted aniline moiety bound to a triphenylphosphoranylidene group, enhancing its stability and versatility in synthetic applications. Its key advantages include its utility in Staudinger-type reactions, where it serves as an effective precursor for iminophosphorane intermediates. Additionally, the electron-withdrawing chloro substituent modulates its reactivity, making it suitable for selective transformations in complex molecular frameworks. This compound is particularly valuable in the synthesis of nitrogen- and phosphorus-containing heterocycles, offering precise control in catalytic and stoichiometric processes. Its well-defined structure ensures reproducibility in research and industrial applications.
Benzenamine,4-chloro-N-(triphenylphosphoranylidene)- structure
31641-65-3 structure
Product Name:Benzenamine,4-chloro-N-(triphenylphosphoranylidene)-
CAS No:31641-65-3
MF:C24H19ClNP
MW:387.8411257267
MDL:MFCD00018599
CID:323455
PubChem ID:277681
Update Time:2025-11-02

Benzenamine,4-chloro-N-(triphenylphosphoranylidene)- Chemical and Physical Properties

Names and Identifiers

    • Benzenamine,4-chloro-N-(triphenylphosphoranylidene)-
    • 4,4'-dichlorobenzanilide
    • 4-Chlor-benzoesaeure-(4-chlor-anilid)
    • 4-chloro-benzoic acid-(4-chloro-anilide)
    • 4-chloro-N-(4-chlorophenyl)-benzamid
    • 4-Chlorophenyliminotriphenylphosphorane
    • AC1L5YVZ
    • AC1Q3RBB
    • N-(p-chlorophenyl)triphenylphosphine imide
    • n1-(4-chlorophenyl)-4-chlorobenzamide
    • NSC41058
    • SureCN611657
    • Triphenylphosphin(N-p-chlorophenyl)imine
    • triphenylphosphine p-chlorophenylimide
    • 31641-65-3
    • NSC-126619
    • [(4-Chlorophenyl)imino](triphenyl)-lambda~5~-phosphane
    • N-(4-CHLOROPHENYL)-P,P,P-TRIPHENYLPHOSPHINE IMIDE
    • Triphenyl[(4-chlorophenyl)imino]phosphorane
    • N1-(1,1,1-TRIPHENYL-LAMBDA5-PHOSPHANYLIDENE)-4-CHLOROANILINE
    • 4-Chloro-N-(triphenylphosphoranylidene)aniline
    • (4-chlorophenyl)imino-triphenyl-lambda5-phosphane
    • NSC126619
    • DTXSID40953607
    • AKOS024319252
    • MDL: MFCD00018599
    • Inchi: 1S/C24H19ClNP/c25-20-16-18-21(19-17-20)26-27(22-10-4-1-5-11-22,23-12-6-2-7-13-23)24-14-8-3-9-15-24/h1-19H
    • InChI Key: FQCORUUEGHMUJZ-UHFFFAOYSA-N
    • SMILES: ClC1C=CC(=CC=1)N=P(C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1

Computed Properties

  • Exact Mass: 387.09457
  • Monoisotopic Mass: 387.0943643g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 1
  • Heavy Atom Count: 27
  • Rotatable Bond Count: 4
  • Complexity: 440
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: 7.1
  • Topological Polar Surface Area: 12.4?2

Experimental Properties

  • PSA: 12.36

Benzenamine,4-chloro-N-(triphenylphosphoranylidene)- Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
Cooke Chemical
S4254452-250MG
N-(4-CHLOROPHENYL)-P,P,P-TRIPHENYLPHOSPHINEIMIDE
31641-65-3 AldrichCPR
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RMB 1012.88 2025-02-20

Additional information on Benzenamine,4-chloro-N-(triphenylphosphoranylidene)-

Comprehensive Overview of Benzenamine,4-chloro-N-(triphenylphosphoranylidene)- (CAS No. 31641-65-3)

Benzenamine,4-chloro-N-(triphenylphosphoranylidene)- (CAS No. 31641-65-3) is a specialized organic compound that has garnered significant attention in recent years due to its unique chemical properties and versatile applications. This compound, often referred to as a phosphine imine derivative, plays a crucial role in modern synthetic chemistry, particularly in the development of novel materials and pharmaceuticals. With the increasing demand for high-performance chemical intermediates, this compound has become a focal point for researchers and industry professionals alike.

The molecular structure of Benzenamine,4-chloro-N-(triphenylphosphoranylidene)- features a chlorinated benzene ring connected to a triphenylphosphoranylidene group, which contributes to its distinctive reactivity. This structural arrangement makes it particularly valuable in nucleophilic substitution reactions and catalysis. Recent studies have highlighted its potential in green chemistry applications, aligning with the global push towards more sustainable industrial processes. As environmental concerns continue to dominate scientific discourse, compounds like this are being reevaluated for their eco-friendly potential.

One of the most significant applications of Benzenamine,4-chloro-N-(triphenylphosphoranylidene)- is in the field of pharmaceutical research. Its unique properties make it an excellent candidate for the synthesis of drug intermediates, particularly in the development of targeted therapies. With the pharmaceutical industry increasingly focusing on precision medicine, the demand for specialized compounds like this has surged. Researchers are particularly interested in its potential role in cancer treatment research, where its molecular structure could be key to developing new therapeutic agents.

In material science, Benzenamine,4-chloro-N-(triphenylphosphoranylidene)- has shown promise in the development of advanced polymers and functional materials. Its ability to act as a ligand in coordination chemistry makes it valuable for creating metal-organic frameworks (MOFs), which have applications in gas storage, separation technologies, and catalysis. The growing interest in smart materials and nanotechnology has further increased the relevance of this compound in cutting-edge research.

The synthesis and handling of Benzenamine,4-chloro-N-(triphenylphosphoranylidene)- require specialized knowledge due to its unique reactivity profile. Modern laboratories employ advanced spectroscopic techniques such as NMR and mass spectrometry for its characterization. The compound's stability under various conditions is a subject of ongoing research, particularly in relation to its potential industrial-scale applications. Recent advancements in process chemistry have made its production more efficient, addressing some of the challenges associated with its synthesis.

Market trends indicate a growing demand for Benzenamine,4-chloro-N-(triphenylphosphoranylidene)-, particularly in regions with strong pharmaceutical and specialty chemicals industries. The Asia-Pacific market has shown particular interest, driven by expanding research capabilities and increasing investment in innovative chemical solutions. Industry analysts predict steady growth in the compound's applications, especially as new uses continue to emerge in biotechnology and material engineering sectors.

From a regulatory perspective, Benzenamine,4-chloro-N-(triphenylphosphoranylidene)- is subject to standard chemical handling protocols. Researchers and manufacturers must adhere to laboratory safety standards and environmental regulations when working with this compound. The scientific community continues to investigate its toxicological profile and environmental impact, with recent studies focusing on its biodegradability and potential green chemistry applications.

The future of Benzenamine,4-chloro-N-(triphenylphosphoranylidene)- appears promising, with ongoing research uncovering new potential applications. Its role in catalysis, material science, and pharmaceutical development continues to expand, making it a compound of significant interest to both academic researchers and industrial chemists. As synthetic methodologies advance and our understanding of its properties deepens, this compound is likely to play an increasingly important role in addressing some of the most pressing challenges in modern chemistry and materials science.

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