3809-28-7 Usage
Description
1, 3, 5, 7, 9, 11, 13, 15-Octacyclohexylpentaene is a unique chemical compound characterized by its linear arrangement of eight cyclohexyl rings with alternating single and double carbon-carbon bonds. This distinctive structure and reactivity make it a valuable component in organic synthesis reactions, serving as a precursor for the production of various organic molecules and polymers. Its chemical properties also render it suitable for the development of advanced materials and pharmaceuticals. Furthermore, due to its conjugated system and electron delocalization, it holds potential applications in the realms of organic electronics and optoelectronics. However, caution is advised when handling this compound due to its potential reactivity and toxicity.
Uses
Used in Organic Synthesis:
1, 3, 5, 7, 9, 11, 13, 15-Octacyclohexylpentaene is used as a key intermediate in organic synthesis for the production of a wide range of organic molecules and polymers. Its unique structure allows for versatile reactivity, making it a valuable asset in the creation of complex molecular structures.
Used in Advanced Material Development:
1 3 5 7 9 11 13 15-OCTACYCLOHEXYLPENTA-& is utilized in the development of advanced materials due to its chemical properties, which can contribute to the enhancement of material performance in various applications.
Used in Pharmaceutical Industry:
1, 3, 5, 7, 9, 11, 13, 15-Octacyclohexylpentaene serves as a precursor in the pharmaceutical industry, where it can be used to synthesize novel drug candidates with potential therapeutic applications.
Used in Organic Electronics and Optoelectronics:
1 3 5 7 9 11 13 15-OCTACYCLOHEXYLPENTA-&'s conjugated system and electron delocalization make it a promising candidate for applications in organic electronics and optoelectronics, where it can be employed in the design and development of innovative electronic devices and optoelectronic systems.
Used in Research and Development:
Due to its unique structure and reactivity, 1, 3, 5, 7, 9, 11, 13, 15-Octacyclohexylpentaene is also used in research and development settings to explore new chemical reactions and investigate its potential applications in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 3809-28-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,8,0 and 9 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 3809-28:
(6*3)+(5*8)+(4*0)+(3*9)+(2*2)+(1*8)=97
97 % 10 = 7
So 3809-28-7 is a valid CAS Registry Number.
3809-28-7Relevant articles and documents
The reactions of dialkyl and diarylethoxysilanes with T6 silsesquioxane cages. X-ray crystallographic studies of the mono-T6D1 and bis-T6D2 insertion ring expansion products
Bassindale, Alan R.,Liu, Zhihua,Parker, David J.,Taylor, Peter G.,Horton, Peter N.,Hursthouse, Michael B.,Light, Mark E.
, p. 1 - 11 (2003)
Successful ring-expanding insertion reactions of T6 silsesquioxane cages using dialkyl and diarylethoxysilanes have been performed to give the first reported mixed T6D1 and T6D2 silsesquioxane cages.
Controlled cleavage of R8Si8O12 frameworks: A revolutionary new method for manufacturing precursors to hybrid inorganic-organic materials
Feher, Frank J.,Soulivong, Daravong,Eklund, Andrew G.
, p. 399 - 400 (2007/10/03)
Cube-octameric polyhedral silsesquioxanes (R8Si8O12) react with strong acids (HX) to produce R8Si8O11X2 frameworks resulting from selective cleavage of one Si-O-Si linkage; subse
