1255147-51-3 Usage
Uses
Used in Pharmaceutical Research:
1-(2,2-diethoxyethyl)-4-iodo-1H-pyrazole is used as a pharmaceutical intermediate for the synthesis of more complex chemical compounds with potential therapeutic properties. The presence of the iodine atom and the diethoxyethyl group allows for further functionalization and the development of new molecules with valuable applications in medicine.
Used in Chemical Synthesis:
In the chemical industry, 1-(2,2-diethoxyethyl)-4-iodo-1H-pyrazole serves as a building block for the creation of more intricate chemical structures. The diethoxyethyl group provides a chemical handle for the introduction of other chemical groups, enabling the exploration of new molecular properties and reactivity.
Used in Radiolabeling and Imaging Studies:
The iodine atom in 1-(2,2-diethoxyethyl)-4-iodo-1H-pyrazole makes it a potential candidate for use in radiolabeling and imaging studies. This application can be particularly useful in the development of diagnostic tools and techniques in the medical field.
Used in Drug Delivery Systems:
1-(2,2-diethoxyethyl)-4-iodo-1H-pyrazole can be employed in the development of novel drug delivery systems, potentially enhancing the delivery, bioavailability, and therapeutic outcomes of various pharmaceutical compounds. Its unique structure and functional groups make it a valuable tool for improving the efficiency and effectiveness of drug administration.
Check Digit Verification of cas no
The CAS Registry Mumber 1255147-51-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,5,5,1,4 and 7 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1255147-51:
(9*1)+(8*2)+(7*5)+(6*5)+(5*1)+(4*4)+(3*7)+(2*5)+(1*1)=143
143 % 10 = 3
So 1255147-51-3 is a valid CAS Registry Number.
1255147-51-3Relevant academic research and scientific papers
Lindsay-Scott, Peter J.,Charlesworth, Natalie G.,Grozavu, Alexandru
, p. 11295 - 11303 (2017)
A four-step protocol for the synthesis of pyrazolo[1,5-a]pyrazines has been developed. Commercially available pyrazoles were alkylated and formylated in a regiocontrolled manner to give pyrazole-5-aldehydes bearing 2,2-dialkoxyethyl substitution on N-1. Efficient conditions for the subsequent deprotection and cyclization of these intermediates allowed access to pyrazolo[1,5-a]pyrazines with multiple substitution patterns. The versatility of the pyrazole-5-aldehyde intermediates was further demonstrated through a deprotection and double-reductive amination sequence to give 4,5,6,7-tetrahydropyrazolo[1,5-a]pyrazines.
