1027079-22-6 Usage
Uses
Used in Pharmaceutical Industry:
5-(4-Methoxyphenoxy)pentanoic Acid Methyl Ester is used as an intermediate in the synthesis of Stigmatellin A, a compound with potential applications in pharmaceutical research. Its role in the preparation of Stigmatellin A makes it valuable for the development of new drugs and therapeutic agents.
Used in Chemical Synthesis:
In the field of chemical synthesis, 5-(4-Methoxyphenoxy)pentanoic Acid Methyl Ester is used as a protected form of the parent acid, allowing for further reactions and modifications. This protected form enables chemists to carry out specific reactions without affecting the functional groups of the molecule, which can be crucial for the synthesis of complex organic compounds.
Used in Research and Development:
5-(4-Methoxyphenoxy)pentanoic Acid Methyl Ester is utilized in research and development for the study of its chemical properties and potential applications. Its role as an intermediate in the synthesis of Stigmatellin A makes it an important compound for understanding the structure-activity relationships and exploring the biological activities of related compounds.
Used in Analytical Chemistry:
In analytical chemistry, 5-(4-Methoxyphenoxy)pentanoic Acid Methyl Ester can be employed as a reference compound or standard for the development and validation of analytical methods. Its clear oil appearance and unique chemical structure make it suitable for use in chromatographic, spectroscopic, and other analytical techniques.
Overall, 5-(4-Methoxyphenoxy)pentanoic Acid Methyl Ester is a versatile compound with applications in various industries, including pharmaceuticals, chemical synthesis, research and development, and analytical chemistry. Its role as an intermediate in the preparation of Stigmatellin A highlights its potential in the development of new drugs and therapeutic agents, while its protected form allows for further exploration of its chemical properties and applications.
Check Digit Verification of cas no
The CAS Registry Mumber 1027079-22-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,7,0,7 and 9 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1027079-22:
(9*1)+(8*0)+(7*2)+(6*7)+(5*0)+(4*7)+(3*9)+(2*2)+(1*2)=126
126 % 10 = 6
So 1027079-22-6 is a valid CAS Registry Number.
1027079-22-6Relevant academic research and scientific papers
Efficient synthesis of an enantiopure β-lactam as an advanced precursor of thrombin and tryptase inhibitors
Annunziata, Rita,Benaglia, Maurizio,Cinquini, Mauro,Cozzi, Franco,Maggioni, Francesco,Puglisi, Alessandra
, p. 2952 - 2955 (2007/10/03)
A new and efficient synthesis of a β-lactam that is an advanced precursor of inhibitors of thrombin and tryptase is reported. The reaction sequence is based on the use of an inexpensive enantiomerically pure starting material and is designed to allow acce
