58684-54-1 Usage
Uses
Used in Pharmaceutical Industry:
(6R-trans)-3-(acetoxymethyl)-7-[(4-chloro-1,3-dioxobutyl)amino]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid is used as an antibiotic for the treatment of various bacterial infections. Its application is based on the compound's ability to interfere with bacterial cell wall synthesis, leveraging the properties of its chemical structure to combat infections effectively.
Additionally, if there are more specific applications in different industries, they can be listed as follows:
Used in Research and Development:
(6R-trans)-3-(acetoxymethyl)-7-[(4-chloro-1,3-dioxobutyl)amino]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid is used as a research compound for studying the mechanisms of antibiotic action and resistance in bacteria. Its application is due to its unique chemical structure, which can provide insights into the development of new antibiotics and strategies to combat antibiotic resistance.
Used in Veterinary Medicine:
(6R-trans)-3-(acetoxymethyl)-7-[(4-chloro-1,3-dioxobutyl)amino]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid is used as a veterinary antibiotic for treating bacterial infections in animals. Its application is based on the compound's potential to effectively target and treat a range of bacterial infections in veterinary patients, contributing to animal health and welfare.
Check Digit Verification of cas no
The CAS Registry Mumber 58684-54-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,6,8 and 4 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 58684-54:
(7*5)+(6*8)+(5*6)+(4*8)+(3*4)+(2*5)+(1*4)=171
171 % 10 = 1
So 58684-54-1 is a valid CAS Registry Number.
InChI:InChI=1/C14H15ClN2O7S/c1-6(18)24-4-7-5-25-13-10(16-9(20)2-8(19)3-15)12(21)17(13)11(7)14(22)23/h10,13H,2-5H2,1H3,(H,16,20)(H,22,23)
58684-54-1Relevant academic research and scientific papers
A new cephalosporin. SCE-963: 7-[2-(2-aminothiazol-4-yl)-acetamido]-3- [[[1-(2-dimethylaminoethyl)-1h-tetrazol-5-yl]-thio]methyl]ceph-3-em-4-carboxylic acid. Chemistry and structure-activity relationships
Numata,Minamida,Yamaoka,Shiraishi,Miyawaki,Akimoto,Naito,Kida
, p. 1262 - 1271 (2007/10/09)
The synthesis and the in vitro and in vivo antimicrobial activities of a series of 7-[2-(2-aminothiazol-4-yl)acetamido]cephalosporins (1) having varied 3-substituents, such as methyl, hydroxymethyl, acetoxymethyl, pyridiniomethyl and heterocyclicthiomethyls, are described. The derivates having five membered heterocyclicthiomethyls exhibited strong inhibitory activities against Gram-negative organisms including some strains od Escherichia coli and Proteus morganii which are insensitive to cefazolin and cephaloridine. Pronounced activities were noted with 7-[2-(2-aminothiazol-4-yl)-acetamido]-3-[[[1-(2-dimethylaminoethyl)-1H-tetra zol-5-yl]thio]methyl]ceph-3-em-4-carboxylic acid (1y;SCE-963).
