228710-82-5 Usage
Description
5-bromo-2-(2,5-dimethyl-1H-pyrrol-1-yl)pyridine is an organic compound characterized by its unique molecular structure, which features a pyridine ring with a bromine atom at the 5th position and a 2,5-dimethyl-1H-pyrrol-1-yl group attached at the 2nd position. 5-bromo-2-(2,5-dimethyl-1H-pyrrol-1-yl)pyridine is known for its reactivity and versatility in organic synthesis, making it a valuable building block for creating a wide range of other organic molecules.
Uses
Used in Organic Synthesis:
5-bromo-2-(2,5-dimethyl-1H-pyrrol-1-yl)pyridine is used as a reactant and reagent for the synthesis of various organic compounds. Its unique structure allows it to participate in a range of chemical reactions, such as cross-coupling, substitution, and condensation reactions, enabling the formation of diverse molecular architectures with potential applications in different fields.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 5-bromo-2-(2,5-dimethyl-1H-pyrrol-1-yl)pyridine is used as a key intermediate in the development of new drugs. Its ability to form a variety of organic compounds makes it a valuable tool for medicinal chemists, who can use it to create novel drug candidates with potential therapeutic properties.
Used in Chemical Research:
5-bromo-2-(2,5-dimethyl-1H-pyrrol-1-yl)pyridine is also utilized in academic and industrial research settings, where it serves as a starting material for exploring new reaction pathways and developing innovative synthetic methods. Its reactivity and structural diversity make it an attractive candidate for studying various aspects of organic chemistry, including reaction mechanisms, stereochemistry, and catalyst design.
Used in Material Science:
In the field of material science, 5-bromo-2-(2,5-dimethyl-1H-pyrrol-1-yl)pyridine can be employed as a building block for designing new materials with specific properties, such as optoelectronic materials, sensors, or advanced polymers. Its unique structure and reactivity allow for the creation of materials with tailored characteristics, which can be applied in various technological applications.
Check Digit Verification of cas no
The CAS Registry Mumber 228710-82-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,8,7,1 and 0 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 228710-82:
(8*2)+(7*2)+(6*8)+(5*7)+(4*1)+(3*0)+(2*8)+(1*2)=135
135 % 10 = 5
So 228710-82-5 is a valid CAS Registry Number.
InChI:InChI=1/C11H11BrN2/c1-8-3-4-9(2)14(8)11-6-5-10(12)7-13-11/h3-7H,1-2H3
228710-82-5Relevant articles and documents
Alternate synthesis of a β-3 adrenergic receptor agonist
Scott, Robert W.,Fox, Darrell E.,Wong, John W.,Burns, Michael P.
, p. 587 - 592 (2004)
Previously our group reported synthetic efforts used to synthesize kilogram quantities of the β-3 receptor agonist (R)-(4-(2-(2-(6-aminopyridin-3-yl)- 2-hydroxyethylamino)ethoxy)phenyl)-acetic acid, 1. Additional research was conducted to explore an alternate chiral route with a streamlined protecting group scheme. The alternate asymmetric process and synthetic rationale are described.
PROLYL HYDROXYLASE INHIBITORS
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Page/Page column 16, (2010/04/03)
The invention described herein relates to certain bicyclic heteroaromatic N-substituted glycine derivatives of formula (I), which are antagonists of HIF prolyl hydroxylases and are useful for treating diseases benefiting from the inhibition of this enzyme, anemia being one example.
NOVEL SULFONAMIDE SUBSTITUTED CHROMAN DERIVATIVES USEFUL AS BETA-3 ADRENORECEPTOR AGONISTS
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Page/Page column 56, (2008/12/07)
This invention relates to novel sulfonamide substituted chroman derivatives which are useful in the treatment of beta-3 receptor mediated conditions.
