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2-(1H-pyrazol-1-yl)-4-tertbutylpyridine is a versatile chemical compound that belongs to the pyrazole and pyridine families. It is characterized by the presence of a pyrazole group and a tert-butyl group on the pyridine ring, which contribute to its electron-donating properties and steric hindrance, respectively. This unique combination of features makes it a promising candidate for various applications in chemical processes.

1361941-59-4

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1361941-59-4 Usage

Uses

Used in Coordination Chemistry:
2-(1H-pyrazol-1-yl)-4-tertbutylpyridine is used as a ligand for the formation of coordination compounds. Its electron-donating pyrazole group and bulky tert-butyl group enable it to chelate with metal ions, forming stable complexes with potential applications in catalysis, sensing, and materials science.
Used in Organic Synthesis:
In the field of organic synthesis, 2-(1H-pyrazol-1-yl)-4-tertbutylpyridine is employed as a building block for the synthesis of various organic compounds. Its steric hindrance and electron-donating properties can be utilized to control reactivity and selectivity in organic reactions, making it a valuable component in the development of new molecules with desired properties.
Used in Pharmaceutical Industry:
2-(1H-pyrazol-1-yl)-4-tertbutylpyridine is used as a starting material or intermediate in the synthesis of pharmaceutical compounds. Its unique structural features can be exploited to design and develop new drugs with improved pharmacological properties, such as enhanced potency, selectivity, and reduced side effects.
Used in Materials Science:
In materials science, 2-(1H-pyrazol-1-yl)-4-tertbutylpyridine can be used as a component in the development of advanced materials with specific properties. Its coordination capabilities and electronic properties can be harnessed to create materials with applications in areas such as optoelectronics, sensors, and energy storage.
Overall, 2-(1H-pyrazol-1-yl)-4-tertbutylpyridine is a versatile and valuable compound with a wide range of potential applications across various industries, including coordination chemistry, organic synthesis, pharmaceuticals, and materials science. Its unique combination of steric hindrance and electron-donating properties makes it a promising candidate for the development of new technologies and products.

Check Digit Verification of cas no

The CAS Registry Mumber 1361941-59-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,6,1,9,4 and 1 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1361941-59:
(9*1)+(8*3)+(7*6)+(6*1)+(5*9)+(4*4)+(3*1)+(2*5)+(1*9)=164
164 % 10 = 4
So 1361941-59-4 is a valid CAS Registry Number.

1361941-59-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(1H-pyrazol-1-yl)-4-tert-butylpyridine

1.2 Other means of identification

Product number -
Other names 2-(1H-pyrazol-1-yl)-4-tertbutylpyridine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
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More Details:1361941-59-4 SDS

1361941-59-4Relevant academic research and scientific papers

Charged cyclometalated iridium(III) complexes that have large electrochemical gap

Shavaleev, Nail M.,Scopelliti, Rosario,Baranoff, Etienne,Graetzel, Michael,Nazeeruddin, Mohammad K.

, p. 316 - 319 (2012)

Bis-cyclometalated cationic Ir(III) diimine complexes [Ir(C^N) 2(N^N)](PF6) with 1-phenylpyrazoles (C^N) and 1-(4′-tert-butyl-2′-pyridyl)pyrazole (N^N) are white solids that have absorption onset below 425 nm and electrochemical gap of up to 3.5 V.

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