64354-26-3 Usage
Uses
Used in Pharmaceutical Industry:
4,6-Dibromo-5-hydroxypicolinic acid is used as a building block for the synthesis of pharmaceutical compounds due to its unique chemical properties and reactivity.
Used in Coordination Chemistry:
4,6-Dibromo-5-hydroxypicolinic acid is used as a ligand in the synthesis of coordination complexes, contributing to the development of new materials with potential applications in various fields.
Used in Organic Synthesis:
4,6-Dibromo-5-hydroxypicolinic acid is used as a reactant in organic synthesis, enabling the creation of new organic compounds with potential applications in various industries.
Used in Catalysis:
4,6-Dibromo-5-hydroxypicolinic acid is used as a catalyst or catalyst precursor in various chemical reactions, enhancing the efficiency and selectivity of these processes.
Check Digit Verification of cas no
The CAS Registry Mumber 64354-26-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,3,5 and 4 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 64354-26:
(7*6)+(6*4)+(5*3)+(4*5)+(3*4)+(2*2)+(1*6)=123
123 % 10 = 3
So 64354-26-3 is a valid CAS Registry Number.
64354-26-3Relevant academic research and scientific papers
Selectively herbicidal 4,6-dibromo-5-hydroxy-2-pyridine carboxamide, salts and esters thereof and methods of preparation and use
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, (2008/06/13)
The invention is a genus of compounds of the formula STR1 wherein X is --OH, --OM, --OR or --NH2 ; Y is H, M or R'C0--; R is a primary or secondary C1 --C12 alkyl group, a C5 --C7 cycloalkyl group, phenyl or a C7 --C12 phenalkyl or alylphenyl group; R' is a C1 --C11 alkyl or alkenyl group, a C5 --C7 cycloalkyl or cycloalkenyl group, phenyl or a C7 --C12 phenyl alkyl, phenylalkenyl, alkylphenyl or alkenylphenyl group and M, independently, is a metal or ammonium cation. The compounds in which X is --NH2 are uniquely selective post-emergent herbicides for control of both broadleaf weeds and wild oats in grains such as wheat and barley. The compounds in which X is not NH2 have utility as intermediates and some of them are biologically active.
