1000018-10-9 Usage
General Description
3-Amino-2,6-dibromo-5-ethoxypyridine is a specialized chemical compound having a pyridine nucleus, which is a basic heterocyclic organic compound. It is a derivative of pyridine, synthesized with amino, bromo, and ethoxy groups attached to the core structure. 3-Amino-2,6-dibromo-5-ethoxypyridine does not occur naturally and is synthesized in laboratories for various chemical experiments and production processes. It appears as a solid in its pure form. The specific physical properties such as melting point, boiling point, density, and solubility of this compound could vary depending on the conditions under which it is processed and stored. Also, precautions need to be taken while handling this chemical due to its reactive nature. As a compound with potential industrial uses, 3-Amino-2,6-dibromo-5-ethoxypyridine may be utilized in the pharmaceutical industry and other sectors like dye and adhesives productions.
Check Digit Verification of cas no
The CAS Registry Mumber 1000018-10-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,0,0,1 and 8 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1000018-10:
(9*1)+(8*0)+(7*0)+(6*0)+(5*0)+(4*1)+(3*8)+(2*1)+(1*0)=39
39 % 10 = 9
So 1000018-10-9 is a valid CAS Registry Number.
1000018-10-9Relevant articles and documents
Creating an antibacterial with in vivo efficacy: Synthesis and characterization of potent inhibitors of the bacterial cell division protein FTSZ with improved pharmaceutical properties
Haydon, David J.,Bennett, James M.,Brown, David,Collins, Ian,Galbraith, Greta,Lancett, Paul,MacDonald, Rebecca,Stokes, Neil R.,Chauhan, Pramod K.,Sutariya, Jignesh K.,Nayal, Narendra,Srivastava, Anil,Beanland, Joy,Hall, Robin,Henstock, Vincent,Noula, Caterina,Rockley, Chris,Czaplewski, Lloyd
supporting information; experimental part, p. 3927 - 3936 (2010/09/04)
3-Methoxybenzamide (1) is a weak inhibitor of the essential bacterial cell division protein FtsZ. Alkyl derivatives of 1 are potent antistaphylococcal compounds with suboptimal drug-like properties. Exploration of the structure-activity relationships of analogues of these inhibitors led to the identification of potent antistaphylococcal compounds with improved pharmaceutical properties.
