59009-62-0 Usage
Uses
Used in Medicinal Chemistry:
2,4-Diphenyl-1H-pyrrole-3-carbonitrile is used as a pharmaceutical intermediate for the synthesis of various organic compounds. Its unique structure and chemical properties make it a promising candidate for the development of new drugs and therapeutic agents.
Used in Material Science:
In the field of material science, 2,4-Diphenyl-1H-pyrrole-3-carbonitrile is utilized for the development of novel materials with specific properties. Its structural features contribute to the creation of materials with potential applications in various industries.
Used in Anticancer Research:
2,4-Diphenyl-1H-pyrrole-3-carbonitrile has been studied for its biological activity, particularly its potential as an anti-cancer agent. Its unique chemical structure may offer new avenues for the development of targeted therapies against various types of cancer.
Used in Synthesis of Organic Compounds:
DPPC is used as a key building block in the synthesis of a wide range of organic compounds. Its versatile structure allows for the formation of various derivatives, which can be further utilized in the development of new chemical entities with diverse applications.
Check Digit Verification of cas no
The CAS Registry Mumber 59009-62-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,0,0 and 9 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 59009-62:
(7*5)+(6*9)+(5*0)+(4*0)+(3*9)+(2*6)+(1*2)=130
130 % 10 = 0
So 59009-62-0 is a valid CAS Registry Number.
59009-62-0Relevant academic research and scientific papers
Cu-catalyzed ring opening reaction of 2H-azirines with terminal alkynes: An easy access to 3-alkynylated pyrroles
Li, Tengfei,Xin, Xiaoyi,Wang, Chunxiang,Wang, Dongping,Wu, Fan,Li, Xincheng,Wan, Boshun
supporting information, p. 4806 - 4809 (2015/04/27)
A highly efficient Cu-catalyzed ring expansion reaction of 2H-azirines with terminal alkynes has been developed. This transformation provides a powerful method for the synthesis of 3-alkynyl polysubstituted pyrroles under mild conditions in good yields. The direct transformation process, specific selectivity, and good tolerance to a variety of substituents make it an alternative approach to the reported protocols.
Base-Induced Cycloaddition of N-(Tosylmethyl)imino Compounds to Michael Acceptors. Synthesis of 2,3,4-Trisubstituted Pyrroles
Houwing, Hendrik A.,van Leusen, Albert M.
, p. 1127 - 1132 (2007/10/02)
A series of N-(tosylmethyl)imino compounds has been prepared, and applied to a new, base induced, one operational synthesis of otherwise more difficulty accesible 2,3,4-trisubstituted pyrroles from electron deficient olefins.This regiospec
