383136-27-4 Usage
Uses
Used in Pharmaceutical Synthesis:
1-(2-Pyrimidinyl)-1H-pyrrole-2-carbaldehyde is utilized as a key intermediate in the synthesis of pharmaceuticals for its potential biological activity. It serves as a building block in the development of new drugs, contributing to the creation of novel therapeutic agents with improved efficacy and selectivity.
Used in Agrochemical Production:
In the agrochemical industry, 1-(2-Pyrimidinyl)-1H-pyrrole-2-carbaldehyde is employed as a precursor in the synthesis of various agrochemicals. Its incorporation into these products can enhance their effectiveness in pest control and crop protection, thereby supporting sustainable agricultural practices.
Used as a Reagent in Organic Synthesis:
1-(2-Pyrimidinyl)-1H-pyrrole-2-carbaldehyde also functions as a reagent in organic synthesis, where it is used to introduce the pyrimidine ring into a range of organic molecules. This capability is valuable for the preparation of complex organic compounds and the exploration of new chemical space in research and development.
Used in Medicinal Chemistry and Drug Discovery:
1-(2-PYRIMIDINYL)-1H-PYRROLE-2-CARBALDEHYDE holds a significant position in medicinal chemistry and drug discovery. It is leveraged to construct new pharmaceuticals with potential therapeutic applications. Its unique structure allows for the design of molecules that can interact with biological targets, leading to the discovery of innovative treatments for various diseases.
Check Digit Verification of cas no
The CAS Registry Mumber 383136-27-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,8,3,1,3 and 6 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 383136-27:
(8*3)+(7*8)+(6*3)+(5*1)+(4*3)+(3*6)+(2*2)+(1*7)=144
144 % 10 = 4
So 383136-27-4 is a valid CAS Registry Number.
InChI:InChI=1/C9H7N3O/c13-7-8-3-1-6-12(8)9-10-4-2-5-11-9/h1-7H
383136-27-4Relevant articles and documents
Cp?Rh(iii) and Cp?Ir(iii)-catalysed redox-neutral C-H arylation with quinone diazides: quick and facile synthesis of arylated phenols
Zhang, Shang-Shi,Jiang, Chun-Yong,Wu, Jia-Qiang,Liu, Xu-Ge,Li, Qingjiang,Huang, Zhi-Shu,Li, Ding,Wang, Honggen
supporting information, p. 10240 - 10243 (2015/06/22)
Cp?Rh(iii)- and Cp?Ir(iii)-catalysed direct C-H arylation with quinone diazides as efficient coupling partners is disclosed. This redox-neutral protocol offers a facile, operationally simple and environmentally benign access to arylated phenols. The reaction represents the first example of Cp?Ir(iii)-catalysed C-H direct arylation reaction.
Cationic triazinium heterocycles by intramolecular NN bond formation
Reeves, Jonathan T.,Han, Zhengxu S.,Goyal, Navneet,Lee, Heewon,Busacca, Carl A.,Senanayake, Chris H.
supporting information, p. 2492 - 2494 (2014/05/06)
Tricyclic heterocycles with a cationic triazinium core were prepared by an intramolecular NN bond forming reaction of an azine oxime precursor. The azine oxime substrates were prepared by SNAr N-arylation of 2-formylpyrroles followed by oxime formation of the formyl moiety. The synthesis was demonstrated with five different azines and several functional groups.
