488799-65-1 Usage
Description
2-[(3-bromophenoxy)methyl]pyridine is a pyridine compound featuring a bromophenyl group attached to the pyridine ring. It is recognized for its unique structure and reactivity, which positions it as a valuable building block and intermediate in organic synthesis and pharmaceutical research. The bromine substitution on the phenyl group endows the molecule with distinctive characteristics, making it a potentially versatile tool across various applications in the chemical and pharmaceutical industries.
Uses
Used in Organic Synthesis:
2-[(3-bromophenoxy)methyl]pyridine is used as a building block for the synthesis of a wide range of organic compounds. Its unique structure allows for the creation of new molecules with specific properties, making it a key component in the development of novel chemical entities.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 2-[(3-bromophenoxy)methyl]pyridine serves as an intermediate in the production of various pharmaceuticals. Its reactivity and the presence of the bromine atom facilitate the synthesis of new drugs with potential therapeutic applications.
Used in Agrochemical Development:
2-[(3-bromophenoxy)methyl]pyridine is also utilized in the agrochemical sector as a precursor for the development of new pesticides and other agrochemical products. Its unique attributes can contribute to the creation of more effective and environmentally friendly solutions for agricultural challenges.
Used in Material Science:
2-[(3-bromophenoxy)methyl]pyridine's versatility extends to material science, where it is used as a component in the development of new materials with specific properties. Its potential applications in this field include the creation of advanced polymers, coatings, and other materials with tailored characteristics for various industries.
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.
