2623-83-8 Usage
Description
2-Bromonanoic acid, with the molecular formula C9H17BrO2, is a carboxylic acid featuring a bromine atom attached to the second carbon of a nine-carbon chain. This chemical compound is widely recognized for its role in the synthesis of pharmaceuticals and organic compounds, serving as a versatile reagent in organic and medicinal chemistry for the development of new drugs and biologically active molecules. Moreover, it functions as a building block in the creation of various esters, amides, and other organic molecules, highlighting its significance in chemical synthesis.
Uses
Used in Pharmaceutical Synthesis:
2-Bromonanoic acid is utilized as a key intermediate in the synthesis of pharmaceuticals, contributing to the development of new drugs and biologically active compounds. Its unique structure allows for various chemical reactions, facilitating the creation of a broad range of medicinal agents.
Used in Organic Compound Synthesis:
As a reagent in organic chemistry, 2-Bromonanoic acid is employed in the synthesis of a variety of organic compounds. Its ability to participate in numerous chemical reactions makes it a valuable component in the formation of complex organic molecules.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, 2-Bromonanoic acid serves as a crucial reagent for research and development. It aids in the exploration of new drug candidates and the enhancement of existing pharmaceuticals, driving advancements in medical treatments.
Used in the Synthesis of Esters and Amides:
2-Bromonanoic acid is used as a building block in the synthesis of esters and amides, which are essential components in various chemical and biological processes. Its presence in these compounds allows for the creation of a diverse array of molecules with potential applications in various industries.
It is important to handle 2-Bromonanoic acid with care due to its corrosive nature, which can cause irritation to the skin, eyes, and respiratory system if not properly managed. Proper safety measures should be taken to minimize risks associated with its use.
Check Digit Verification of cas no
The CAS Registry Mumber 2623-83-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,6,2 and 3 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2623-83:
(6*2)+(5*6)+(4*2)+(3*3)+(2*8)+(1*3)=78
78 % 10 = 8
So 2623-83-8 is a valid CAS Registry Number.
InChI:InChI=1/C9H17BrO2/c1-2-3-4-5-6-7-8(10)9(11)12/h8H,2-7H2,1H3,(H,11,12)
2623-83-8Relevant articles and documents
Synthesis and biological evaluation of novel N-α-haloacylated homoserine lactones as quorum sensing modulators
Syrpas, Michail,Ruysbergh, Ewout,Stevens, Christian V.,De Kimpe, Norbert,Mangelinckx, Sven
, p. 2539 - 2549 (2015/02/19)
Novel N-α-haloacylated homoserine lactones, in which a halogen atom was introduced at the α-position of the carbonyl function of the N - acyl chain, have been studied as quorum sensing (QS) modulators and compared with a library of natural N - acylated homoserine lactones (AHLs). The series of novel analogues consists of α-chloro, α-bromo and α-iodo AHL analogues. Furthermore, the biological QS activity of the synthetic AHL analogues compared to the natural AHLs was evaluated. Halogenated analogues demonstrated a reduced activity in the Escherichia coli JB523 bioassay, with the α-iodo lactones being the less active ones and the α-chloro AHLs the most potent QS agonists. Most of the α-haloacylated analogues did not exhibit a significant reduction when tested in the QS inhibition test. Therefore, these novel analogues could be utilized as chemical probes for QS structure-activity studies.
