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CAS:50428-39-2 | 1,3-DINEOPENTYLIDYNE-2-PROPANOL

CAS:50428-39-2 | 1,3-DINEOPENTYLIDYNE-2-PROPANOL

Molecular Formula:C13H20O
Molecular Weight:192.3
Purity:98%
Package:1g 5g 25g
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Product Introduction

Introduction of CAS:50428-39-2 | 1,3-DINEOPENTYLIDYNE-2-PROPANOL

 

"2,2,8,8-Tetramethyl-3,6-nonadiyn-5-ol" is a chemical compound with the molecular formula C13H20O . It is a solid substance at 20°C . The compound has a molecular weight of 192.3 ."2,2,8,8-Tetramethyl-3,6-nonadiyn-5-ol" is a solid substance at 20°C . It has a molecular weight of 192.3 . The compound has a melting point range of 78.0 to 82.0°C .

 

Specification of CAS:50428-39-2 | 1,3-DINEOPENTYLIDYNE-2-PROPANOL

 

ITEMS

SPECIFICATION

Melt point

80 °C

Purity

97%

Molecular Formula

C13H20O

Molecular Weight

192.3

 

Research Application of CAS:50428-39-2 | 1,3-DINEOPENTYLIDYNE-2-PROPANOL

Polymerization Catalyst

Vanadium complexes, including those related to 2,2,8,8-Tetramethyl-3,6-nonadiyn-5-ol, serve as efficient catalysts in olefin polymerization. These catalysts are explored for ethylene polymerization and copolymerization with other monomers, demonstrating the potential of such complexes in the field of polymer science (Ji-Qian Wu & Yue-sheng Li, 2011).

Synthesis of Functionalized Compounds

The compound plays a role in the synthesis of various functionalized organic compounds. For instance, it is used in phosphine-catalyzed annulations to create highly functionalized tetrahydropyridines, showcasing its versatility in organic synthesis (Xue-Feng Zhu, J. Lan, & O. Kwon, 2003).

Catalysis in Coupling Reactions

It is also involved in coupling reactions of aryl bromides with alkynols, catalyzed by a tetraphosphine/palladium catalyst. This application highlights its importance in creating diverse chemical bonds and structures (M. Feuerstein, H. Doucet, & M. Santelli, 2004).

Polymer Formation and Isomerization

The compound contributes to the formation of polymers and isomerization processes. For example, its derivative plays a role in the synthesis of a septicyclic compound through polymer formation and subsequent isomerization (J. Dale, C. Ramming, & M. R. Suissa, 1993).

Optoelectronic Properties

In the field of optoelectronics, derivatives of 2,2,8,8-Tetramethyl-3,6-nonadiyn-5-ol are used to create molecular wires with unique optoelectronic properties. This application is crucial for the development of new electronic and photonic materials (Changsheng Wang, L. Pålsson, A. Batsanov, & M. Bryce, 2006).

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