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Bicyclo[2.1.1]hexane, 1-ethenyl-5,5-dimethyl-, commonly known as norbornene, is a chemical compound characterized by its bicyclic structure and a vinyl group. With the molecular formula C8H12, norbornene exists as a colorless liquid with a distinct pungent odor. It is widely recognized for its applications in the production of polymers, plastics, and cycloolefin copolymers, as well as its utility in organic synthesis and as a reagent in various chemical reactions. However, due to its flammable nature and potential to cause skin or eye irritation, careful handling is advised.

16626-39-4

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16626-39-4 Usage

Uses

Used in Polymer and Plastics Industry:
Norbornene is utilized as a monomer in the production of advanced polymers and plastics, particularly for the synthesis of cycloolefin copolymers. Its unique bicyclic structure contributes to the enhanced properties of the resulting materials, such as improved strength, durability, and heat resistance.
Used in Organic Synthesis:
As a versatile building block in organic synthesis, norbornene is employed in the synthesis of a variety of organic compounds. Its reactivity and stability make it a valuable component in the creation of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Chemical Reactions as a Reagent:
Norbornene serves as a reagent in numerous chemical reactions, facilitating the formation of desired products through its participation in processes such as metathesis, Diels-Alder reactions, and other cycloadditions. Its ability to engage in these reactions makes it an indispensable tool in the field of organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 16626-39-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,6,2 and 6 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 16626-39:
(7*1)+(6*6)+(5*6)+(4*2)+(3*6)+(2*3)+(1*9)=114
114 % 10 = 4
So 16626-39-4 is a valid CAS Registry Number.

16626-39-4Relevant academic research and scientific papers

Efficient triplet-triplet energy transfer using clay-bound ionic sensitizers

Madhavan,Pitchumani

, p. 9041 - 9044 (2007/10/03)

Both cationic and anionic clays, with sensitizers anchored onto their interlayer by ionic linkage, are found to be useful 'microreactors' to achieve triplet state reactivity of myrcene in an experimentally simple, inexpensive and clean reaction. These clay-bound sensitizers are characterized by X-ray and their advantages are highlighted.

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