99909-62-3 Usage
Uses
Used in Pharmaceutical Industry:
5-ISOPROPYL-3-(METHOXYCARBONYL)-2H-CYCLOHEPTA[B]FURAN-2-ONE is used as a key intermediate in the synthesis of various pharmaceuticals for its potential biological and pharmacological activities. Its unique structure allows for the development of compounds with therapeutic applications.
Used in Agrochemical Industry:
5-ISOPROPYL-3-(METHOXYCARBONYL)-2H-CYCLOHEPTA[B]FURAN-2-ONE is used as a building block in the synthesis of agrochemicals, contributing to the development of effective and environmentally friendly products.
Used in Antimicrobial Applications:
5-ISOPROPYL-3-(METHOXYCARBONYL)-2H-CYCLOHEPTA[B]FURAN-2-ONE is used as an antimicrobial agent for its potential to inhibit the growth of various microorganisms, making it a promising candidate for the development of new antimicrobial drugs.
Used in Antitumor Applications:
5-ISOPROPYL-3-(METHOXYCARBONYL)-2H-CYCLOHEPTA[B]FURAN-2-ONE is used as an antitumor agent for its potential to exhibit antitumor properties, offering a new avenue for the development of cancer treatments.
Used in Organic Synthesis:
5-ISOPROPYL-3-(METHOXYCARBONYL)-2H-CYCLOHEPTA[B]FURAN-2-ONE is used as a valuable building block in organic synthesis, enabling the preparation of diverse organic compounds with potential applications in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 99909-62-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,9,0 and 9 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 99909-62:
(7*9)+(6*9)+(5*9)+(4*0)+(3*9)+(2*6)+(1*2)=203
203 % 10 = 3
So 99909-62-3 is a valid CAS Registry Number.
InChI:InChI=1/C14H14O4/c1-8(2)9-5-4-6-11-10(7-9)12(13(15)17-3)14(16)18-11/h4-8H,1-3H3
99909-62-3Relevant academic research and scientific papers
Synthesis and analysis of positive inotropic effects of 3-substituted-2H-cyclohepta[b]furan-2-one derivatives
Yokota,Yanagisawa,Kosakai,Wakabayashi,Tomiyama,Yasunami
, p. 865 - 871 (2007/10/02)
Several 3-substituted-2H-cyclohepta[h]furan-2-one derivatives were prepared and tested in vitro for positive inotropic character. Introduction of an isopropyl group at the 5-position of compound 8a caused an increase of PIC50 (negative logarithm of the dosage which increases the contractile force by 50%) from 4.48 to 5.10. Among the 5-isopropyl-8-alkoxy compounds, the isopropoxy compound 12f had the most potent activity with a PIC50 value of 5.99. Conversion of the ester group at the 3-position to a methylene group and of the alkoxy group at the 8-position to a substituted amino group caused a decrease in activity. The most active compound, 12f, was also found to bave a weaker heart rate (HR)-increasing effect compared to milrinone and amrinone.
