14764-90-0 Usage
Uses
Used in Organic Synthesis:
2,6-Diiodo-3-hydroxypyridine is used as a building block in organic synthesis for the preparation of various pharmaceuticals and agrochemicals. Its presence of iodine atoms and a hydroxyl group allows for a wide range of chemical reactions, contributing to the development of new and improved compounds in these fields.
Used in Materials Science:
In the field of materials science, 2,6-Diiodo-3-hydroxypyridine is employed in the production of dyes and pigments. Its chemical structure provides specific color properties, making it a useful component in the creation of various colorants for different applications.
Used as an Intermediate in Synthesis:
2,6-Diiodo-3-hydroxypyridine also serves as an intermediate in the synthesis of other organic compounds. Its unique structure and reactivity make it a key component in the production of a variety of chemical products, further expanding its utility in the chemical industry.
Used in Chemical Research:
As a valuable reagent, 2,6-Diiodo-3-hydroxypyridine is commonly used in laboratories for its distinctive properties. Researchers leverage its reactivity to explore new chemical pathways and develop innovative applications, contributing to the advancement of chemical science.
Check Digit Verification of cas no
The CAS Registry Mumber 14764-90-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,7,6 and 4 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 14764-90:
(7*1)+(6*4)+(5*7)+(4*6)+(3*4)+(2*9)+(1*0)=120
120 % 10 = 0
So 14764-90-0 is a valid CAS Registry Number.
14764-90-0Relevant academic research and scientific papers
RING-FUSED MORPHOLINE DERIVATIVE HAVING PI3K-INHIBITING ACTIVITY
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Page/Page column 33, (2011/07/30)
The present invention provides compounds or a pharmaceutically acceptable salt thereof which inhibit the activity of PI3K to regulate many biological processes including the growth, differentiation, survival, proliferation, migration, metabolism, and the like of cells and are therefore useful for the prophylaxis/therapy of diseases including inflammatory diseases, arteriosclerosis, vascular/circulatory diseases, cancer/tumors, immune system diseases, cell proliferative diseases, infectious diseases, and the like. The above problem was solved by providing a ring-fused morpholine compound shown in the present specification, or a pharmaceutically acceptable salt thereof.
Synthesis of the phenylpyridal scaffold as a helical peptide mimetic
Bourne, Gregory T.,Kuster, Daniel J.,Marshall, Garland R.
supporting information; experimental part, p. 8439 - 8445 (2010/09/08)
Phenylpyridal- and phenyldipyridal-based scaffolds have been designed and synthesized as novel helical peptide mimetics. The synthesis required optimisation and selective alkylation in producing 2,6-functionalized 3-hydroxypyridine derivatives for a convergent scheme. The pyridine analogues were coupled by a series of Suzuki/Stille types cross-coupling reactions. A series of biaryl and ter-aryl substituted heterocycles were produced. The synthetic approach was concise and high yielding allowing large variability at the wanted sidechain attachment points. A number of compounds were synthesised to show the versatility of the strategy.
