2623-83-8 Usage
General Description
2-Bromonanoic acid is a chemical compound with the molecular formula C9H17BrO2. It is a carboxylic acid with a bromine atom attached to the second carbon of a nine-carbon chain. This chemical is commonly used in the synthesis of pharmaceuticals and organic compounds. It is also utilized as a reagent in organic and medicinal chemistry, particularly in the development of new drugs and biologically active compounds. Additionally, 2-Bromonanoic acid can be used as a building block in the synthesis of various esters, amides, and other organic molecules. It is important to handle 2-Bromonanoic acid with care, as it is corrosive and can cause irritation to the skin, eyes, and respiratory system if not handled properly.
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.
