7234-76-6

Basic information

• Product Name: zinc, chlorozinc, [(diphenyl-trimethylsilylimino-phosphoranyl)methylene-diphenyl-phosphoranyl]-trimethylsilyl-azanide
• CAS NO: 7234-76-6
• Molecular Formula: C₁₅H₁₃N
• Molecular Weight: 1380.6637
• Mol File: 7234-76-6.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 613.8°C at 760 mmHg
• Flash Point: 325°C
• Vapor Pressure: 5.29E-15mmHg at 25°C
• CAS DataBase Reference: zinc, chlorozinc, [(diphenyl-trimethylsilylimino-phosphoranyl)methylene-diphenyl-phosphoranyl]-trimethylsilyl-azanide(CAS DataBase Reference)
• NIST Chemistry Reference: zinc, chlorozinc, [(diphenyl-trimethylsilylimino-phosphoranyl)methylene-diphenyl-phosphoranyl]-trimethylsilyl-azanide(7234-76-6)
• EPA Substance Registry System: zinc, chlorozinc, [(diphenyl-trimethylsilylimino-phosphoranyl)methylene-diphenyl-phosphoranyl]-trimethylsilyl-azanide(7234-76-6)

Safety Data

• Hazardous Substances Data: 7234-76-6(Hazardous Substances Data)

Usage

General Description

Zinc is a metallic element commonly used in a variety of industrial and consumer products. Chlorozinc is a compound that combines zinc with chlorine, often used in chemical reactions and as a reagent in organic synthesis. The complex chemical compound [(diphenyl-trimethylsilylimino-phosphoranyl)methylene-diphenyl-phosphoranyl]-trimethylsilyl-azanide is a highly specialized and potentially reactive substance with a complex molecular structure containing zinc and phosphorus atoms, as well as silicon and nitrogen. zinc, chlorozinc, [(diphenyl-trimethylsilylimino-phosphoranyl)methylene-diphenyl-phosphoranyl]-trimethylsilyl-azanide likely has specific applications in chemical research and manufacturing due to its unique composition and properties.

Upstream product

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Downstream Products

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Relevant articles and documents

Pd-Catalyzed Dearomatization of Indole Derivatives via Intermolecular Heck Reactions?

Pd-catalyzed intermolecular dearomative Heck reaction of indoles with aryl iodides is described. The challenges on both reactivity and regioselectivity are addressed by the judicious regulation of the geometric and electronic properties of the substrates. An array of indoline derivatives bearing C2-quaternary center is obtained in good to excellent yields (up to 93%) with exclusive regioselectivity under operationally simple conditions. The mechanistic proposal is supported by detailed DFT calculations.

Comparison of performance between benzoindoline and indoline dyes in zinc oxide dye-sensitized solar cell

The cell performance of novel benzoindoline dyes on zinc oxide prepared by template cathode electro-deposition method was compared with that of known indoline dyes. Among cyanoacrylic, single and double rhodanine acetic acid derivatives, the cyanoacrylic