97944-43-9 Usage
General Description
4-Amino-5-bromo-3-methylpyridine is a chemical compound with the molecular formula C6H7BrN2. It is a derivative of pyridine and contains an amino group, a bromine atom, and a methyl group attached to the pyridine ring. This chemical is commonly used in the pharmaceutical and agrochemical industries for the synthesis of various compounds, including pharmaceutical drugs and crop protection products. It is known for its versatile reactivity and can be used as a building block in organic synthesis. Additionally, it is a valuable intermediate in the production of other chemical compounds. Due to its unique structure and properties, 4-amino-5-bromo-3-methylpyridine has applications in a wide range of chemical processes and industries.
Check Digit Verification of cas no
The CAS Registry Mumber 97944-43-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,9,4 and 4 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 97944-43:
(7*9)+(6*7)+(5*9)+(4*4)+(3*4)+(2*4)+(1*3)=189
189 % 10 = 9
So 97944-43-9 is a valid CAS Registry Number.
InChI:InChI=1/C6H7BrN2/c1-4-2-9-3-5(7)6(4)8/h2-3H,1H3,(H2,8,9)
97944-43-9Relevant articles and documents
NOVEL INHIBITOR COMPOUNDS OF PHOSPHODIESTERASE TYPE 10A
-
, (2013/02/28)
The present invention relates to novel carboxamide compounds, pharmaceutical compositions containing them, and their use in therapy. The compounds possess valuable therapeutic properties and are particularly suitable for treating or controlling medical disorders selected from neurological disorders and psychiatric disorders, for ameliorating the symptoms associated with such disorders and for reducing the risk of such disorders
Bromination of Pyridines. II. Bromination of Aminopicolines
Dunn, A. D.,Currie, A.,Hayes, L. E.
, p. 369 - 374 (2007/10/02)
The bromination of all ten possible aminopicolines 1-10 was investigated.In general, the major brominated product was that corresponding to electrophilic attack at the sites para or ortho to the amino group.