87226-88-8 Usage
Chemical structure
1,3,5-Tri-o-tolylbenzene is a chemical compound with three tolyl (methylphenyl) groups attached to a central benzene ring.
Family
It belongs to the family of triarylmethanes.
Usage
Commonly used in organic synthesis as a building block for the preparation of various organic compounds.
Physical properties
It is a colorless, odorless solid at room temperature.
Solubility
Insoluble in water.
Applications
Mainly used in the production of dyes, pigments, and pharmaceuticals.
Structural versatility
Due to its structural versatility, it can participate in various chemical reactions.
Potential applications
Has potential applications in the development of organic light-emitting diodes (OLEDs) and other optoelectronic devices.
Stability
Exhibits high thermal and chemical stability.
Industrial and research applications
1,3,5-Tri-o-tolylbenzene has a wide range of industrial and research applications.
Check Digit Verification of cas no
The CAS Registry Mumber 87226-88-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,2,2 and 6 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 87226-88:
(7*8)+(6*7)+(5*2)+(4*2)+(3*6)+(2*8)+(1*8)=158
158 % 10 = 8
So 87226-88-8 is a valid CAS Registry Number.
87226-88-8Relevant academic research and scientific papers
A ruthenium-based catalytic system with switchable selectivity between cyclotrimerization and enyne metathesis/Diels-Alder reactions of terminal alkynes
Karabulut, Solmaz,Sariaslan, Begüm,?ztürk, Bengi ?zgün
, p. 12 - 16 (2013/08/23)
In this study, we report a practical catalytic system, [RuCl 2(p-cymene)]2/IPr (IPr: 1,3-bis(2,6 diisopropylphenyl) imidazol-2-ylidene), that can switch between cyclotrimerization and cross enyne metathesis. The cyclotrimerization reaction of phenylacetylene catalyzed by [RuCl2(p-cymene)]2 can be switched to enyne metathesis by the introduction of a sterically hindered N-heterocyclic carbene. The 1,3-diene formed during this reaction reacts with dienophiles to form the Diels-Alder adduct. A practical one-pot synthesis method, utilizing enyne metathesis/Diels-Alder reactions, was used to construct cyclic compounds in an efficient manner.
