160233-29-4 Usage
Description
1-Benzyl-3-(tert-butyl)-1H-pyrazole-5-carbonyl chloride is a chemical compound characterized by the molecular formula C17H19ClN2O. It is a carbonyl chloride derivative of the pyrazole ring, which is a heterocyclic compound with a nitrogen-containing five-membered ring. 1-BENZYL-3-(TERT-BUTYL)-1H-PYRAZOLE-5-CARBONYL CHLORIDE is recognized for its reactivity and versatility, making it a valuable building block in the field of organic synthesis. Its role as a key intermediate in the production of pharmaceuticals and agrochemicals, as well as its utility in the preparation of various functionalized pyrazole derivatives, underscores its importance in chemical research and development.
Uses
Used in Pharmaceutical Industry:
1-Benzyl-3-(tert-butyl)-1H-pyrazole-5-carbonyl chloride is used as a key intermediate for the synthesis of pharmaceuticals. Its unique structure and reactivity allow for the development of new drugs with potential therapeutic applications, including the treatment of various diseases and conditions.
Used in Agrochemical Industry:
In the agrochemical sector, 1-Benzyl-3-(tert-butyl)-1H-pyrazole-5-carbonyl chloride serves as a crucial component in the creation of new agrochemicals. Its incorporation into these products can lead to the development of more effective pesticides, herbicides, and other agricultural chemicals that enhance crop protection and yield.
Used in Organic Synthesis:
As a building block in organic synthesis, 1-Benzyl-3-(tert-butyl)-1H-pyrazole-5-carbonyl chloride is utilized for the preparation of a wide range of functionalized pyrazole derivatives. These derivatives can be further modified and applied in various chemical processes, contributing to the advancement of chemical research and the discovery of novel compounds with diverse applications.
Used in Chemical Research and Development:
1-BENZYL-3-(TERT-BUTYL)-1H-PYRAZOLE-5-CARBONYL CHLORIDE's versatility and reactivity make it an essential tool in chemical research and development. It is employed in the exploration of new synthetic pathways, the synthesis of complex molecules, and the investigation of reaction mechanisms, all of which contribute to the expansion of chemical knowledge and the creation of innovative products.
Check Digit Verification of cas no
The CAS Registry Mumber 160233-29-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,0,2,3 and 3 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 160233-29:
(8*1)+(7*6)+(6*0)+(5*2)+(4*3)+(3*3)+(2*2)+(1*9)=94
94 % 10 = 4
So 160233-29-4 is a valid CAS Registry Number.
InChI:InChI=1/C15H17ClN2O/c1-15(2,3)13-9-12(14(16)19)18(17-13)10-11-7-5-4-6-8-11/h4-9H,10H2,1-3H3