79171-99-6 Usage
Uses
Used in Chemical Industry:
[1,1'-Biphenyl]-4-carboxylic acid, hexahydro-2-oxo-4-(3-oxo-4-phenoxy-1-butenyl)-2H-cyclopenta[b]furan-5-yl ester, [3aR-[3aα,4α(E),5β,6aα]](9CI) is used as a key intermediate in the synthesis of various specialty chemicals and pharmaceuticals. Its unique structure and properties enable it to serve as a building block for the development of new compounds with specific functionalities and applications.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, [1,1'-Biphenyl]-4-carboxylic acid, hexahydro-2-oxo-4-(3-oxo-4-phenoxy-1-butenyl)-2H-cyclopenta[b]furan-5-yl ester, [3aR-[3aα,4α(E),5β,6aα]](9CI) is utilized as a precursor for the synthesis of novel drug candidates. Its unique molecular structure allows for the development of compounds with potential therapeutic applications, such as in the treatment of various diseases and disorders.
Used in Drug Delivery Systems:
[1,1'-Biphenyl]-4-carboxylic acid, hexahydro-2-oxo-4-(3-oxo-4-phenoxy-1-butenyl)-2H-cyclopenta[b]furan-5-yl ester, [3aR-[3aα,4α(E),5β,6aα]](9CI) can also be employed in the design and development of drug delivery systems. Its unique properties may enable the creation of innovative formulations that improve the bioavailability, stability, and targeted delivery of therapeutic agents, ultimately enhancing their efficacy and safety.
Check Digit Verification of cas no
The CAS Registry Mumber 79171-99-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,1,7 and 1 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 79171-99:
(7*7)+(6*9)+(5*1)+(4*7)+(3*1)+(2*9)+(1*9)=166
166 % 10 = 6
So 79171-99-6 is a valid CAS Registry Number.
79171-99-6Relevant articles and documents
He fluorine front row element intermediate preparation method (by machine translation)
-
, (2018/05/16)
The invention discloses he fluorine front row element intermediate, i.e. formula 5 compound preparation method, including the use of biphenyl formyl protected Corey lactone as raw materials, through oxidation, HWE connected side chain, fluorinated, hydrolysis of deprotection step. Preparation method of this invention has the operability is strong, stable process, intermediates for the preparation of white powder, good stability. (by machine translation)
N-(Methanesulfonyl)-16-phenoxyprostaglandincarboxamides: Tissue-Selective, Uterine Stimulants
Schaaf, Thomas K.,Bindra, Jasjit S.,Eggler, James F.,Plattner, Jacob J.,Nelson, A. James,et al.
, p. 1353 - 1359 (2007/10/02)
In an effort to develop tissue-selective prostaglandin analogues resistant to the metabolic inactivating pathways of the natural materials, hybrid compounds modified both at C-1 with a sulfonimide moiety and in the n-amylcarbinol side chain with substituted phenoxy groups were synthesized and evaluated in a variety of in vitro and in vivo models.Several of these analogues exhibited potent, tissue-selective, uterine stimulant activity, a finding subsequently confirmed in clinical studies with one member of this series, N-(methanesulfonyl)-16-phenoxy-ω-tetranor-PGE2-carboxamide (CP-34089/ZK-57671, sulprostone).
