213337-42-9 Usage
Uses
Used in Organic Synthesis:
2-(Bromomethyl)quinoline hydrobromide is used as a reagent in organic synthesis for the functionalization of aromatic compounds. Its unique structure allows for the introduction of various functional groups to aromatic rings, facilitating the synthesis of complex organic molecules.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-(Bromomethyl)quinoline hydrobromide is utilized for the development of potential drug candidates. Its quinoline core and bromomethyl functionality provide a versatile scaffold for the design and synthesis of new therapeutic agents with diverse biological activities.
Used in Chemical Research:
2-(Bromomethyl)quinoline hydrobromide is also employed in chemical research for studying the reactivity and selectivity of various organic reactions. Its unique properties enable researchers to explore new reaction pathways and develop innovative synthetic methods.
Used in Material Science:
Although not explicitly mentioned in the provided materials, 2-(Bromomethyl)quinoline hydrobromide could potentially be used in material science for the development of new materials with specific properties, such as optoelectronic materials, sensors, or catalysts, due to its quinoline-based structure and functionalizable bromomethyl group.
Check Digit Verification of cas no
The CAS Registry Mumber 213337-42-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,3,3,3 and 7 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 213337-42:
(8*2)+(7*1)+(6*3)+(5*3)+(4*3)+(3*7)+(2*4)+(1*2)=99
99 % 10 = 9
So 213337-42-9 is a valid CAS Registry Number.
213337-42-9Relevant articles and documents
STIMULI - OR BIO- RESPONSIVE COPOLYMERS, THE POLYMERSOMES COMPRISING THE SAME AND THEIR USE IN DRUG DELIVERY
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, (2021/06/22)
The present invention concerns amphiphilic copolymers that may be photo- or redox-cleavable and that may assemble into polymersomes. It also concerns their process of preparation and their use as drug carriers.
