488799-65-1 Usage
General Description
The chemical 2-[(3-bromophenoxy)methyl]pyridine is a pyridine compound with a bromophenyl group attached to the pyridine ring. It is commonly used in organic synthesis and pharmaceutical research as a building block or intermediate for the production of various compounds. Its unique structure and reactivity make it a valuable tool for creating new pharmaceuticals, agrochemicals, and materials. The bromine substitution on the phenyl group adds interesting characteristics to the molecule, making it potentially useful for a variety of applications in the chemical and pharmaceutical industries. Overall, 2-[(3-bromophenoxy)methyl]pyridine is a versatile and important compound in the field of organic chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 488799-65-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,8,8,7,9 and 9 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 488799-65:
(8*4)+(7*8)+(6*8)+(5*7)+(4*9)+(3*9)+(2*6)+(1*5)=251
251 % 10 = 1
So 488799-65-1 is a valid CAS Registry Number.
488799-65-1Relevant articles and documents
Palladium-Catalyzed Regioselective Synthesis of 1-Hydroxycarbazoles Under Aerobic Conditions
Youn, So Won,Kim, Young Ho,Jo, Yoon Hyung
supporting information, p. 462 - 468 (2019/01/04)
A palladium-catalyzed aerobic C?H amidation of N-Ts-2-amino-3′-hydroxylbiaryls has been developed to afford a diverse range of 1-hydroxycarbazoles with high regioselectivity and efficiency. This protocol benefits from operational simplicity, robustness, a
Design and synthesis of oxadiazolidinediones as inhibitors of plasminogen activator inhibitor-1
Gopalsamy, Ariamala,Kincaid, Scott L.,Ellingboe, John W.,Groeling, Thomas M.,Antrilli, Thomas M.,Krishnamurthy, Girija,Aulabaugh, Ann,Friedrichs, Gregory S.,Crandall, David L.
, p. 3477 - 3480 (2007/10/03)
A novel series of PAI-1 inhibitors containing an oxadiazolidinedione moiety were identified by high through-put screening. Optimization of substituents by parallel synthesis and the iterative design toward understanding structure-activity relationship to improve potency are described.
