634205-29-1 Usage
Molecular structure
1-Phenazinecarboxylic acid, 6-[(1R)-1-[[2-methyl-6-(2-propenyloxy)benzoyl]oxy]ethyl]-, 2-propenyl ester has a complex structure consisting of a phenazinecarboxylic acid core and a 6-[(1R)-1-[[2-methyl-6-(2-propenyloxy)benzoyl]oxy]ethyl]-, 2-propenyl ester group.
Functional groups
The compound contains various functional groups, including a carboxylic acid group, an ester group, and an alkene group (2-propenyl).
Stereochemistry
The compound has a specific stereochemistry, with the (1R) configuration at the ethyl group attached to the phenazine core.
Potential applications
1-Phenazinecarboxylic acid, 6-[(1R)-1-[[2-methyl-6-(2-propenyloxy)benzoyl]oxy]ethyl]-, 2-propenyl ester may have potential applications in pharmaceuticals, agrochemicals, and materials science due to its unique structure and properties.
Research and development
Further testing and study are needed to fully understand the potential uses and implications of 1-Phenazinecarboxylic acid,
6-[(1R)-1-[[2-methyl-6-(2-propenyloxy)benzoyl]oxy]ethyl]-, 2-propenyl
ester in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 634205-29-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,3,4,2,0 and 5 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 634205-29:
(8*6)+(7*3)+(6*4)+(5*2)+(4*0)+(3*5)+(2*2)+(1*9)=131
131 % 10 = 1
So 634205-29-1 is a valid CAS Registry Number.
634205-29-1Relevant academic research and scientific papers
First synthesis of racemic saphenamycin and its enantiomers. Investigation of biological activity
Laursen, Jane B.,Jorgensen, Charlotte G.,Nielsen, John
, p. 723 - 731 (2007/10/03)
The natural antibiotic saphenamycin, 6-[1-(2-hydroxy-6-methyl-benzoyloxy)-ethyl]-phenazine-1-carboxylic acid, was synthesized from saphenic acid using temporary allyl protection of carboxy and phenoxy functionalities. Resolution of racemic saphenic acid was performed by crystallization of the corresponding (-)-brucine diastereomeric salts and the absolute configuration of (-)-brucinium (-)-saphenate was determined by X-ray crystallography to have R-configuration. This also proved to be the configuration of natural saphenic acid. Enantiomers of saphenamycin were obtained from resolved saphenic acid and screened against a range of skin flora and resistant Staphylococcus aureus strains. Biological activities of saphenamycin enantiomers were compared with that of the synthetic racemate as well as earlier reported activities of saphenamycin isolated from natural sources. No significant difference was observed in activity of the enantiomers of saphenamycin, which revealed that the chirality of saphenamycin has no consequences for the antibiotic activity. Saphenamycin proved to be a potent antibiotic against fusidic acid and rifampicin resistant S. aureus strains showing MIC of 0.1-0.2 μg/mL. 2002 Elsevier Science. All rights reserved.
