67738-67-4 Usage
Uses
Used in Pharmaceutical Industry:
[3aa,4a(E),5b,6aa]-4-[4-(3-Chlorophenoxy)-3-oxo-1-butenyl]hexahydro-5-hydroxy-2H-cyclopenta[b]furan-2-one is used as a potential drug candidate for its possible biological activity. The presence of a cyclopentafuran ring and a butenyl side chain with a chlorine substituent, along with a hydroxyl group and a keto-alkene functional group, may contribute to its pharmacological properties, making it a subject of interest for further research and development in the pharmaceutical sector.
Used in Chemical Research:
In the field of chemical research, [3aa,4a(E),5b,6aa]-4-[4-(3-Chlorophenoxy)-3-oxo-1-butenyl]hexahydro-5-hydroxy-2H-cyclopenta[b]furan-2-one is utilized for studying the synthesis and properties of complex organic molecules. Its unique structure provides opportunities for exploring novel chemical reactions and mechanisms, potentially leading to the discovery of new compounds with various applications.
Used in Biochemical Studies:
[3aa,4a(E),5b,6aa]-4-[4-(3-Chlorophenoxy)-3-oxo-1-butenyl]hexahydro-5-hydroxy-2H-cyclopenta[b]furan-2-one is employed in biochemical studies to investigate its interactions with biological systems. The molecule's structure and functional groups may allow it to bind to specific biological targets or enzymes, offering insights into its potential role in biological processes and its use in developing new therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 67738-67-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,7,3 and 8 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 67738-67:
(7*6)+(6*7)+(5*7)+(4*3)+(3*8)+(2*6)+(1*7)=174
174 % 10 = 4
So 67738-67-4 is a valid CAS Registry Number.
67738-67-4Relevant articles and documents
Intramolecular Acetalization of 5-Hydroxy Ketones and Enones. A Novel Transformation of Important Prostaglandin Intermediates under Acidic Conditions
Schwarz, Sigfrid,Weber, Gisela,Palme, Hans-Joachim,Wentzke, Manfred
, p. 751 - 756 (2007/10/02)
Intermediates in the synthesis of ω-tetranor 16-aryloxy prostaglandins, which are 5-hydroxy enones undergo quantitative intramolecular transformation into cyclic methyl acetals in acidic methanolic solution.The reaction proceeds via the corresponding 5-hydroxy-3-methoxy ketones, which partly exist as hemiacetals.The structure of the compounds investigated was elucidated by 1H NMR spectroscopy and by X-ray analysis of the acetal (11).
PROSTANOIDS. XIX. THE SYNTHESIS OF 14C-LABELED CLOPROSTENOL
Miftakhov, M. S.,Vostrikov, N. S.,Kuznetsov, O. M.,Kuvatov, Yu. G.,Murinov, Yu. I.,Tolstikov, G. A.
, p. 1072 - 1075 (2007/10/02)
A 1:3400 mixture of 2-14C-labelled methyl bromoacetate with the nonradioactive ester gave labelled dimethoxy-2-oxo-3-(m-chlorophenoxy)phosphonate which was used for the synthesis of 16-14C-labelled cloprostenol by the Corey strategy.
