143729-84-4 Usage
General Description
The chemical compound "(2S,5R,6R)-3,3-dimethyl-7-oxo-6-[[2-phenyl-2-[[(2E)-2-[(4-propoxybenzoyl)hydrazinylidene]acetyl]amino]acetyl]amino]-4-thia-1-azabicyclo[3.2. 0]heptane-2-carboxylic acid" is a complex molecule with a heterocyclic structure. It contains a carboxylic acid group and several amino acid residues, as well as a phenyl group. The compound is a derivative of the antibiotic cephalosporin, and is commonly used as an antibacterial agent. Its specific chemical structure gives it the ability to inhibit the synthesis of bacterial cell walls, making it effective in treating a wide range of bacterial infections.
Check Digit Verification of cas no
The CAS Registry Mumber 143729-84-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,3,7,2 and 9 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 143729-84:
(8*1)+(7*4)+(6*3)+(5*7)+(4*2)+(3*9)+(2*8)+(1*4)=144
144 % 10 = 4
So 143729-84-4 is a valid CAS Registry Number.
InChI:InChI=1/C28H31N5O7S/c1-4-14-40-18-12-10-17(11-13-18)23(35)32-29-15-19(34)30-20(16-8-6-5-7-9-16)24(36)31-21-25(37)33-22(27(38)39)28(2,3)41-26(21)33/h5-13,15,20-22,26H,4,14H2,1-3H3,(H,30,34)(H,31,36)(H,32,35)(H,38,39)/b29-15+/t20?,21-,22+,26-/m1/s1
143729-84-4Relevant articles and documents
New ampicillin derivatives with glyoxyloylbenzhydrazones as side chains
Heinisch,Hanschke,Willitzer,Mollmann,Tresselt,Stengel,Eckardt,Kleinwachter
, p. 412 - 415 (2007/10/02)
New ampicillin derivatives were synthesized from glyoxylic acid benzhydrazones by reaction with chloroformates via mixed anhydrides and ampicillin. These compounds were tested in an agar diffusion test against six different bacterial strains and also for their stability against β-lactamases. Studies about structure activity relationships have shown, that the activity against different bacterial strains is influenced in different manner by hydrophilic or hydrophobic and electronic properties of substituents.