89791-76-4 Usage
General Description
2-Amino-3-nitro-4,6-dimethyl-5-bromopyridine is a chemical compound with the molecular formula C7H8BrN3O2. It is a brominated derivative of pyridine, a six-membered heterocyclic ring with five carbon atoms and one nitrogen atom. The compound contains an amino group, a nitro group, and two methyl groups in the 4 and 6 positions of the pyridine ring. 2-Amino-3-nitro-4,6-dimethyl-5-bromopyridine is mainly used in organic synthesis and pharmaceutical research, where it is used as an intermediate in the production of various pharmaceuticals and agrochemicals. It is also used in the development of new materials and complex organic molecules due to its unique structure and reactivity.
Check Digit Verification of cas no
The CAS Registry Mumber 89791-76-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,7,9 and 1 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 89791-76:
(7*8)+(6*9)+(5*7)+(4*9)+(3*1)+(2*7)+(1*6)=204
204 % 10 = 4
So 89791-76-4 is a valid CAS Registry Number.
89791-76-4Relevant articles and documents
SOMATOSTATIN MODULATORS AND USES THEREOF
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Paragraph 00376; 00377, (2019/08/29)
Described herein are compounds that are somatostatin modulators, methods of making such compounds, pharmaceutical compositions and medicaments comprising such compounds, and methods of using such compounds in the treatment of conditions, diseases, or disorders that would benefit from modulation of somatostatin activity.
Syntheses of two potential food mutagens
Tanga,Bradford,Bupp,Kozocas
, p. 569 - 573 (2007/10/03)
The syntheses of the potential heterocyclic amine food mutagens 1,4,6-trimethyl-2-aminoimidazo[4,5-c]pyridine and 1,5,7-trimethyl-2 -aminoimidazo [4,5-b]pyridine are described.
PYRIDYL IMIDAZOLE DERIVATIVES AND PROCESSES FOR THE PREPARATION THEREOF
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, (2008/06/13)
Substituted pyridyl imidazole derivatives of formula (I) inhibit effectively the action of angiotensin II and have a superior anti-hypertensive activity. STR1