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2,4,6-tris(3-(1H-pyrazol-1-yl)phenyl)-1,3,5-triazine is a triazine derivative featuring a symmetrical structure with three 3-(1H-pyrazol-1-yl)phenyl groups attached to the 2, 4, and 6 positions of the triazine ring. This chemical compound is known for its unique structural and electronic properties, positioning it as a promising candidate for a variety of applications in material science, organic synthesis, and pharmaceutical research.

352196-01-1

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352196-01-1 Usage

Uses

Used in Material Science:
2,4,6-tris(3-(1H-pyrazol-1-yl)phenyl)-1,3,5-triazine is used as a component in the development of new materials due to its unique structural and electronic properties, which can contribute to the creation of advanced materials with specific characteristics for various applications.
Used in Organic Synthesis:
In the field of organic synthesis, 2,4,6-tris(3-(1H-pyrazol-1-yl)phenyl)-1,3,5-triazine serves as a key intermediate or building block for the synthesis of complex organic molecules, potentially leading to the discovery of new compounds with novel properties and functions.
Used in Pharmaceutical Research:
2,4,6-tris(3-(1H-pyrazol-1-yl)phenyl)-1,3,5-triazine is utilized as a starting material or a scaffold in the design and synthesis of new pharmaceutical agents. Its unique structure may offer advantages in drug discovery, such as improved binding affinity, selectivity, or pharmacokinetic properties.
Further studies are being conducted to explore the full potential of 2,4,6-tris(3-(1H-pyrazol-1-yl)phenyl)-1,3,5-triazine and its applications across different industries.

Check Digit Verification of cas no

The CAS Registry Mumber 352196-01-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,2,1,9 and 6 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 352196-01:
(8*3)+(7*5)+(6*2)+(5*1)+(4*9)+(3*6)+(2*0)+(1*1)=131
131 % 10 = 1
So 352196-01-1 is a valid CAS Registry Number.

352196-01-1Downstream Products

352196-01-1Relevant academic research and scientific papers

Peripheral modification of 1,3,5-triazine based electron-transporting host materials for sky blue, green, yellow, red, and white electrophosphorescent devices

Chen, Hsiao-Fan,Wang, Ting-Chih,Lin, Shih-Wei,Hung, Wen-Yi,Dai, Hung-Chi,Chiu, Hao-Chih,Wong, Ken-Tsung,Ho, Meng-Huan,Cho, Ting-Yi,Chen, Chieh-Wei,Lee, Chung-Chun

supporting information; experimental part, p. 15620 - 15627 (2012/09/05)

A systematic comparison of the physical properties and the dual-role (host and electron transport) applications of star-shaped 1,3,5-triazine-based ET-type hosts (T2T, 3N-T2T, 3P-T2T, and oCF3-T2T) with differential peripheral groups was reported. The introduction of N-heterocyclic polar peripheries onto a 1,3,5-triazine core gave evident benefits to the electron injection/transport properties, rendering efficient PhOLEDs with a simpler device configuration feasible. Among these hosts, 3P-T2T can serve both as a promising host and electron-transport material for various Ir-based electrophosphorescence devices. These PhOLEDs configured with the same device structure exhibited low operation voltages with a maximum ηext of 8%, 15.7%, 16.9%, 16.4% and 10.8% for sky blue (FIrpic), green [(PPy)2Ir(acac)], yellow [(Bt)2Ir(acac)], red [(Mpq)2Ir(acac)] and white [FIrpic + 0.5 wt%(Mpq)2Ir(acac)], respectively.

Solvent-free preparation of tris-pyrazolyl-1,3,5-triazines

De La Hoz, Antonio,Díaz-Ortiz, Angel,Elguero, José,Martínez, Luis J.,Moreno, Andrés,Sánchez-Migallón, Ana

, p. 4397 - 4403 (2007/10/03)

Tris-pyrazolyl-1,3,5-triazines have been prepared by cyclotrimerization of aromatic nitriles in solvent-free conditions. The interesting structures of these compounds make them candidates for application in coordination chemistry and crystal engineering.

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