5173-11-5

Basic information

• Product Name: 6,13-dioxaheptacyclo[9.3.1.1~4,8~.0~2,10~.0~3,9~.0~5,7~.0~12,14~]hexadecane
• CAS NO: 5173-11-5
• Molecular Formula: C₁₄H₁₆O₂
• Molecular Weight: 216.2756
• Mol File: 5173-11-5.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 381.8°C at 760 mmHg
• Flash Point: 160.2°C
• Density: 1.422g/cm³
• Vapor Pressure: 1.08E-05mmHg at 25°C
• Refractive Index: 1.659
• CAS DataBase Reference: 6,13-dioxaheptacyclo[9.3.1.1~4,8~.0~2,10~.0~3,9~.0~5,7~.0~12,14~]hexadecane(CAS DataBase Reference)
• NIST Chemistry Reference: 6,13-dioxaheptacyclo[9.3.1.1~4,8~.0~2,10~.0~3,9~.0~5,7~.0~12,14~]hexadecane(5173-11-5)
• EPA Substance Registry System: 6,13-dioxaheptacyclo[9.3.1.1~4,8~.0~2,10~.0~3,9~.0~5,7~.0~12,14~]hexadecane(5173-11-5)

Safety Data

• Hazardous Substances Data: 5173-11-5(Hazardous Substances Data)

Upstream product

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Relevant articles and documents

Pd-catalyzed one-pot sequential unsymmetrical cross-coupling reactions of aryl/heteroaryl 1,2-dihalides

Efficient, step-economic, Pd(ii)-catalyzed one-pot sequential Sonogashira/Sonogashira, Sonogashira/Suzuki, Sonogashira/Heck, Suzuki/Sonogashira, Suzuki/Suzuki, Suzuki/Heck, Heck/Sonogashira, Heck/Suzuki and Heck/Heck cross coupling reactions of sterically hindered aryl/heteroaryl 1,2-dihalides have been developed. The present methodology allows the conversion of easily available aryl/heteroaryl 1,2-dihalides into synthetically useful unsymmetrically substituted arenes/heteroarenes in good to excellent yields under mild reaction conditions. This methodology is a powerful tool for building a versatile substrate which can be utilized for the synthesis of various organic scaffolds.