42743-23-7 Usage
Uses
Used in Pharmaceutical Industry:
[1,1'-Biphenyl]-4-carboxylic acid, hexahydro-4-(3-hydroxy-3-methyl-1-octenyl)-2-oxo-2H-cyclopenta[b]furan-5-ester, [3aR-[3aa,4a(1E,3S),5b,6aa]]is used as a pharmaceutical compound for its potential therapeutic properties. The carboxylic acid and ester groups, along with the hexahydro-4-(3-hydroxy-3-methyl-1-octenyl)-2-oxo moiety, may contribute to its bioactivity and interactions with biological targets, making it a candidate for drug development.
Used in Agrochemical Industry:
In the agrochemical industry, [1,1'-Biphenyl]-4-carboxylic acid, hexahydro-4-(3-hydroxy-3-methyl-1-octenyl)-2-oxo-2H-cyclopenta[b]furan-5-ester, [3aR-[3aa,4a(1E,3S),5b,6aa]]may be utilized as an active ingredient in pesticides or herbicides. Its unique structure and functional groups could provide selective control of pests or weeds, offering an alternative to existing agrochemicals.
Used in Materials Science:
[1,1'-Biphenyl]-4-carboxylic acid, hexahydro-4-(3-hydroxy-3-methyl-1-octenyl)-2-oxo-2H-cyclopenta[b]furan-5-ester, [3aR-[3aa,4a(1E,3S),5b,6aa]]can be employed in materials science for the development of novel materials with specific properties. The molecule's structure and functional groups may contribute to the creation of new polymers, coatings, or other materials with unique characteristics, such as enhanced stability, reactivity, or selectivity.
Check Digit Verification of cas no
The CAS Registry Mumber 42743-23-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,7,4 and 3 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 42743-23:
(7*4)+(6*2)+(5*7)+(4*4)+(3*3)+(2*2)+(1*3)=107
107 % 10 = 7
So 42743-23-7 is a valid CAS Registry Number.
42743-23-7Relevant academic research and scientific papers
PROCESS FOR THE PREPARATION OF CARBOPROST AND ITS TROMETHAMINE SALT
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Page/Page column 12, (2017/06/24)
The subject of the invention is a novel process for the preparation of Carboprost tromethamine salt where alkylation the enone of the general formula (II) is carried out in the presence of a chiral auxiliary in aprotic solvent with a Grignard reagent. The methyl ester epimers of formula (VII) are separated by gravity silicagel chromatography and the salt formation is carried out by using solid tromethamine base.
