516508-80-8 Usage
Description
(+/-)-4-[2-(diethylamino)ethoxy]-3,5-diiodophenyl[2-(3-hydroxybutyl)benzofuran-3-yl]methanone hydrochloride is a complex organic compound with a molecular structure that features a phenyl ring with various functional groups, including diethylaminoethoxy and hydroxybutylbenzofuran moieties. (+/-)-4-[2-(diethylamino)ethoxy]-3,5-diiodophenyl[2-(3-hydroxybutyl)benzofuran-3-yl]methanone hydrochloride is characterized by its unique chemical properties and potential applications in various fields.
Uses
Used in Pharmaceutical Industry:
(+/-)-4-[2-(diethylamino)ethoxy]-3,5-diiodophenyl[2-(3-hydroxybutyl)benzofuran-3-yl]methanone hydrochloride is used as an active pharmaceutical ingredient for the development of new drugs targeting specific ion channels. Its unique molecular structure allows it to act as a non-selective ion channel blocker, which can be beneficial in treating various arrhythmic conditions.
Used in Chemical Synthesis:
In the field of organic chemistry, (+/-)-4-[2-(diethylamino)ethoxy]-3,5-diiodophenyl[2-(3-hydroxybutyl)benzofuran-3-yl]methanone hydrochloride serves as a key intermediate in the synthesis of various complex molecules. Its versatile structure can be further modified to produce a wide range of compounds with potential applications in different industries.
Used in Polymer Science:
(+/-)-4-[2-(diethylamino)ethoxy]-3,5-diiodophenyl[2-(3-hydroxybutyl)benzofuran-3-yl]methanone hydrochloride can be utilized as an initiator in ring-opening polymerization reactions. Its alkyne alcohol functionality enables the formation of meta-depside bonds, which can be used to create novel polymeric materials with specific properties.
Used in Drug Delivery Systems:
(+/-)-4-[2-(diethylamino)ethoxy]-3,5-diiodophenyl[2-(3-hydroxybutyl)benzofuran-3-yl]methanone hydrochloride can also be employed in the development of drug delivery systems, particularly for targeted drug delivery. Its unique structure can be exploited to enhance the bioavailability and therapeutic outcomes of various drugs, making it a valuable asset in the field of pharmaceutical research and development.
Check Digit Verification of cas no
The CAS Registry Mumber 516508-80-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,1,6,5,0 and 8 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 516508-80:
(8*5)+(7*1)+(6*6)+(5*5)+(4*0)+(3*8)+(2*8)+(1*0)=148
148 % 10 = 8
So 516508-80-8 is a valid CAS Registry Number.
516508-80-8Relevant articles and documents
Identifying a selective substrate and inhibitor pair for the evaluation of CYP2J2 activity
Lee, Caroline A.,Jones III,Katayama, Jonathan,Kaspera, Ruediger,Jiang, Ying,Freiwald, Sascha,Smith, Evan,Walker, Gregory S.,Totah, Rheem A.
, p. 943 - 951 (2012)
CYP2J2, an arachidonic acid epoxygenase, is recognized for its role in the first-pass metabolism of astemizole and ebastine. To fully assess the role of CYP2J2 in drug metabolism, a selective substrate and potent specific chemical inhibitor are essential.
