14025-98-0 Usage
Uses
Used in Organic Chemistry:
2,3,5-Heptatriene, (5E)is used as a starting material for the production of various other compounds and materials. It is employed in the synthesis and reaction studies, contributing to the development of new organic compounds and materials.
Used in Chemical Production:
2,3,5-Heptatriene, (5E)is used as a precursor in the production of various compounds and materials, playing a crucial role in the chemical industry. Its versatility as a starting material allows for the creation of a wide range of products.
Safety Considerations:
Due to its flammability and potential health effects, 2,3,5-Heptatriene, (5E)is considered a potentially hazardous chemical. It should be handled and used with caution to minimize risks associated with its properties. Proper safety measures, such as using protective equipment and following safety protocols, are essential when working with 2,3,5-Heptatriene, (5E)-.
Check Digit Verification of cas no
The CAS Registry Mumber 14025-98-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,0,2 and 5 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 14025-98:
(7*1)+(6*4)+(5*0)+(4*2)+(3*5)+(2*9)+(1*8)=80
80 % 10 = 0
So 14025-98-0 is a valid CAS Registry Number.
14025-98-0Relevant academic research and scientific papers
Chemistry of gem-Dihalocyclopropanes. XX. The Effect of Methyl and Phenyl Substituents on the Vinylcyclopropylidene-Cyclopentenylidene Rearrangement
Holm, Kjetil H.,Skatteboel, Lars
, p. 783 - 794 (2007/10/02)
Reactions of gem-dibromocyclopropanes of the general structure 1 with methyllithium have been studied.In the most cases cyclopentadienes and/or vinylallenes are the products formed.The results obtained give evidence of a profound substituent effect on the carbene-carbene rearrangement leading to cyclopentadienes.We believe the effect is essentially steric in origin.The results support the mechanism proposed for the rearrangement.
