61563-26-6 Usage
Uses
Used in Pharmaceutical Industry:
2,3-Dibromobenzaldehyde is used as a precursor for the synthesis of various pharmaceuticals, contributing to the development of new drugs and therapeutic agents. Its chemical properties make it a valuable component in the creation of medicinal compounds.
Used in Agrochemical Industry:
In the agrochemical sector, 2,3-Dibromobenzaldehyde serves as a precursor, playing a crucial role in the production of pesticides and other agricultural chemicals that are essential for crop protection and enhancement of yield.
Used in Dye and Perfume Industry:
2,3-Dibromobenzaldehyde is utilized as an intermediate in the production of dyes, which are vital for coloring textiles, plastics, and other materials. Additionally, it is employed in the creation of perfumes, where its chemical structure contributes to the development of unique fragrances.
Used in Organic Synthesis:
As a building block in organic synthesis, 2,3-Dibromobenzaldehyde is instrumental in the synthesis of a variety of aromatic compounds. Its structural features facilitate the formation of complex organic molecules, which are essential in various chemical and industrial applications.
Used as a Reagent in Organic Reactions:
2,3-Dibromobenzaldehyde also functions as a reagent in organic reactions, enabling chemists to carry out specific transformations and syntheses. Its reactivity and selectivity make it a preferred choice for certain types of chemical processes.
Check Digit Verification of cas no
The CAS Registry Mumber 61563-26-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,5,6 and 3 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 61563-26:
(7*6)+(6*1)+(5*5)+(4*6)+(3*3)+(2*2)+(1*6)=116
116 % 10 = 6
So 61563-26-6 is a valid CAS Registry Number.
InChI:InChI=1/C7H4Br2O/c8-6-3-1-2-5(4-10)7(6)9/h1-4H
61563-26-6Relevant academic research and scientific papers
Pharmaceutical compositions and methods of inhibiting phenylethanolamine N-methyltransferase
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, (2008/06/13)
Pharmaceutical compositions and methods of inhibiting phenylethanolamine N-methyltransferase using 7 and/or 8 substituted 1,2,3,4-tetrahydroisoquinoline compounds.
7 AND 8-Halo substituted 1,2,3,4-tetrahydroisoquinoline compounds
-
, (2008/06/13)
1,2,3,4-Tetrahydroisoquinoline compounds having 7 and 8 halo substituents are inhibitors of phenylethanolamine N-methyltransferase.
