17293-59-3 Usage
Description
(1-methylhexane-1,3,5-triyl)trisbenzene is a chemical compound with the molecular formula C33H39. It is a branched alkane with aromatic groups, consisting of a central hexane molecule with three benzene rings attached to it.
Uses
Used in Organic Synthesis:
(1-methylhexane-1,3,5-triyl)trisbenzene is used as a building block in organic synthesis for its unique structure and potential to form more complex organic molecules.
Used in Polymer Production:
(1-methylhexane-1,3,5-triyl)trisbenzene is used as a starting material in the production of polymers due to its ability to form stable and versatile polymer structures.
Used in Pharmaceutical Industry:
(1-methylhexane-1,3,5-triyl)trisbenzene is used as a starting material in the synthesis of pharmaceuticals, potentially contributing to the development of new drugs and therapeutic agents.
Used in Industrial Chemical Production:
(1-methylhexane-1,3,5-triyl)trisbenzene is used in the production of various industrial chemicals, taking advantage of its chemical properties and reactivity.
Used in Material Development:
(1-methylhexane-1,3,5-triyl)trisbenzene may have properties that make it useful in the development of new materials, although further research and testing would be necessary to explore these potential applications.
Check Digit Verification of cas no
The CAS Registry Mumber 17293-59-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,2,9 and 3 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 17293-59:
(7*1)+(6*7)+(5*2)+(4*9)+(3*3)+(2*5)+(1*9)=123
123 % 10 = 3
So 17293-59-3 is a valid CAS Registry Number.
InChI:InChI=1/C25H28/c1-20(22-12-6-3-7-13-22)18-25(24-16-10-5-11-17-24)19-21(2)23-14-8-4-9-15-23/h3-17,20-21,25H,18-19H2,1-2H3
17293-59-3Relevant articles and documents
Regiochemistry of the styrene insertion with CH2-bridged ansa-zirconocene-based catalysts
Izzo, Lorella,Napoli, Mariagrazia,Oliva, Leone
, p. 9340 - 9345 (2007/10/03)
Methylenebis(indenyl)zirconium dichloride substituted in C(3), activated by methylalumoxane, is able to give polystyrene and ethylene-styrene copolymers. In this study hydrooligomers, whose structure, determined by 13C NMR and GC-MS techniques, gives information about the regiochemistry and the stereochemistry of styrene insertion, have been purposefully prepared. The regiochemistry of the styrene insertion is related to the encumbrance of substituents in C(3). rac-[Methylene-(3-R-1-indenyl)2]ZrCl2 with R = H, CH3, or CH2CH3 induces a prevailingly secondary styrene insertion into the zirconium-carbon bond. With increasing the substituent's steric hindrance (R = CH(CH3)2), regiochemistry inversion occurs and the primary insertion becomes prevailing. The analysis of ethylene-styrene copolymers obtained in the presence of the different catalysts allows confirming the correlation between regiochemistry and comonomers' reactivity. Besides, also the stereospecificity can be evaluated from the structure of the hydrotrimers, when the insertion is primary. Whereas the isospecificity in the absence of substituents (secondary insertion) and in the presence of the tert-butyl substituent (primary insertion) is well-known, a surprising syndiospecificity is observed when the indenyl ligand bears the isopropyl substituent in C(3).
