2843-50-7 Usage
Uses
Used in Organic Synthesis:
2,3-dibromobicyclo[2.2.1]heptane is used as a building block for the synthesis of various organic compounds due to its stable and rigid molecular structure, which facilitates the formation of desired products in chemical reactions.
Used in Pharmaceutical Production:
In the pharmaceutical industry, 2,3-dibromobicyclo[2.2.1]heptane is utilized as a key intermediate in the synthesis of certain drugs, contributing to the development of new medications with improved therapeutic properties.
Used in Agrochemical Production:
2,3-dibromobicyclo[2.2.1]heptane is employed in the production of agrochemicals, such as pesticides and herbicides, where its chemical properties can be harnessed to enhance the effectiveness of these products in agricultural applications.
Used as a Chiral Auxiliary in Asymmetric Synthesis:
2,3-dibromobicyclo[2.2.1]heptane has been studied for its potential use as a chiral auxiliary in asymmetric synthesis, where it can help achieve enantioselective reactions, leading to the production of enantiomerically pure compounds with specific biological activities.
Used in Antimicrobial and Antifungal Applications:
2,3-dibromobicyclo[2.2.1]heptane has been shown to exhibit antimicrobial and antifungal properties, making it a potential candidate for use in the development of new antimicrobial agents to combat resistant pathogens.
Check Digit Verification of cas no
The CAS Registry Mumber 2843-50-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,4 and 3 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2843-50:
(6*2)+(5*8)+(4*4)+(3*3)+(2*5)+(1*0)=87
87 % 10 = 7
So 2843-50-7 is a valid CAS Registry Number.
2843-50-7Relevant academic research and scientific papers
Cross-linked Poly-(4-vinylpyridine-styrene)-Bromine Complexes as Stereoselective Brominating Agents
Johar, Y.,Zupan, M.,Sket, B.
, p. 2059 - 2062 (2007/10/02)
Cross-linked poly(styrene-4-vinylpyridine) beads, containing 40-43percent of pyridine rings, were transformed with bromine to provide three types of brominating agents (1), (2), and (3).Reactions of cis- and trans-1-phenylpropene with (1), (2), and (3) resulted in a high degree of anti-stereoselectivity.The reactivity increases from (1) to (3); solvent polarity had no significant effect on stereoselectivity, but affects the reactivity, being significantly greater in acetonitrile and chloroform than in cyclohexane and dioxan.Bromination of 1-phenylcyclohexene with (1) and (3) resulted in the formation of trans-1,2-dibromo-1-phenylcyclohexane (9) and 3-bromo-2-phenylcyclohexene (10), the temperature affecting only the ratio of the products.Bromonation of norbornene with the reagents (1), (2) and (3) resulted in the formation of seven products: 2-exo-bromonorbornane (12), 7-bromonortricyclane (13), 2-exo,3-endo-dibromonorbornane (14), 2-exo-7-anti-dibromonorbornane (15), 2-exo,5-endo-dibromonorbornane (16), 2-exo,5-exo-dibromonorbornane (17), and 2-exo,7-syn-dibromonorbornane (18).
