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Sodium; (5R,6R)-3-((R)-(Z)-2-acetylamino-ethenesulfinyl)-6-((S)-1-hydroxy-ethyl)-7-oxo-1-aza-bicyclo[3.2.0]hept-2-ene-2-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

83916-41-0

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83916-41-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 83916-41-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,9,1 and 6 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 83916-41:
(7*8)+(6*3)+(5*9)+(4*1)+(3*6)+(2*4)+(1*1)=150
150 % 10 = 0
So 83916-41-0 is a valid CAS Registry Number.

83916-41-0Downstream Products

83916-41-0Relevant academic research and scientific papers

Synthesis and biological activities of the Z isomers of carbapenem antibiotics

Harada,Tsubotani,Asai,Okonogi,Kondo

, p. 753 - 757 (1983)

Naturally occurring carbapenem antibiotics having a double bond in the side chain, when refluxed in chloroform containing quarternary alkylammonium halides, were converted into Z isomers in high yields. The mechanism of this new equilibration involved intramolecular proton transfer from the carboxylic acid to the carbon α to the sulfur atom in the side chain as shown by deuterium-labeling experiments. Some Z isomers showed stronger protective effects in mice infected by Escherichia coli O-111 and more potent synergistic activities with cefotiam in mice infected by Proteus vulgaris GN4815 than did the naturally occurring E isomers. The decompositon rates of the Z isomers in mouse kidney homogenates were about 3-fold slower than those of the E isomers.

Synthesis and biological activities of the Z isomers of carbapenem antibiotics

Harada,Tsubotani,Asai,Okonogi,Kondo

, p. 271 - 275 (1983)

Naturally occurring carbapenem antibiotics having a double bond in the side chain, when refluxed in chloroform containing quarternary alkylammonium halides, were converted into Z isomers in high yields. The mechanism of this new equilibration involves intramolecular proton transfer from the carboxylic acid to the carbon α to the sulfur atom in the side chain as shown by deuterium-labeling experiments. Some Z isomers showed stronger protective effects in mice infected by Escherichia coli O-111 and more potent synergistic activities with cefotiam in mice infected by Proteus vulgaris GN4815 than did the naturally occurring E isomers. The decomposition rates of the Z isomers in mouse kidney homogenates were about 3-fold slower than those of the E isomers.

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