902837-39-2 Usage
Uses
Used in Pharmaceutical Industry:
3-BROMO-5-IODO-PYRIDIN-4-YLAMINE is used as a key building block for the synthesis of pharmaceutical drugs. Its unique structure allows for the creation of new molecules with potential therapeutic properties, contributing to drug discovery and development.
Used in Agrochemicals:
In the agrochemical sector, 3-BROMO-5-IODO-PYRIDIN-4-YLAMINE serves as an intermediate in the synthesis of biologically active compounds designed to protect crops and enhance agricultural productivity.
Used in Dyes and Pigments Production:
3-BROMO-5-IODO-PYRIDIN-4-YLAMINE is utilized as an intermediate in the production of dyes and pigments, where its chemical properties contribute to the development of colorants with specific characteristics for various applications.
Used in Organic Synthesis:
As a chemical reagent, 3-BROMO-5-IODO-PYRIDIN-4-YLAMINE is crucial in organic synthesis, enabling the creation of complex organic molecules for research and commercial purposes, highlighting its importance in scientific exploration and innovation.
Check Digit Verification of cas no
The CAS Registry Mumber 902837-39-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,0,2,8,3 and 7 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 902837-39:
(8*9)+(7*0)+(6*2)+(5*8)+(4*3)+(3*7)+(2*3)+(1*9)=172
172 % 10 = 2
So 902837-39-2 is a valid CAS Registry Number.
InChI:InChI=1/C5H4BrIN2/c6-3-1-9-2-4(7)5(3)8/h1-2H,(H2,8,9)
902837-39-2Relevant academic research and scientific papers
NOVEL NAPHTHYRIDINES AND ISOQUINOLINES AND THEIR USE AS CDK8/19 INHIBITORS
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Paragraph 0867; 0868, (2016/02/12)
The present invention relates to naphthyridine and isoquinoline compounds, and pharmaceutically acceptable compositions thereof, useful as inhibitors of CDK8/19, and for the treatment of CDK8/19-related disorders.
Palladium-catalyzed synthesis of 2,3-disubstituted 5-azaindoles via heteroannulation reaction and of 2-substituted 5-azaindoles through domino sila-Sonogashira/5-endo cyclization
Livecchi, Marion,Calvet, Geraldine,Schmidt, Frederic
experimental part, p. 5006 - 5016 (2012/07/03)
A general and efficient procedure for the synthesis of 2,3-disubstituted 5-azaindoles through the palladium-catalyzed heteroannulation of 4-acetamido-3-iodopyridines and diaryl-, dialkyl-, or arylalkylalkynes is described along with a study of the reactio
