64140-56-3 Usage
Description
1-(2,3-dihydro-1H-indol-1-yl)-3-(piperidin-1-yl)propan-1-one is a complex chemical compound featuring a 1H-indol-1-yl group and a piperidin-1-yl group connected to a propan-1-one backbone. As a ketone, it possesses a unique structure that may exhibit pharmaceutical properties due to the presence of the indole and piperidine moieties, which are known to be part of various biologically active compounds. 1-(2,3-dihydro-1H-indol-1-yl)-3-(piperidin-1-yl)propan-1-one holds promise for further exploration in medicinal chemistry and drug discovery, as well as potential applications in synthetic organic chemistry for creating related chemical entities.
Uses
Used in Pharmaceutical Research:
1-(2,3-dihydro-1H-indol-1-yl)-3-(piperidin-1-yl)propan-1-one is used as a compound of interest in pharmaceutical research for its potential medicinal properties. The presence of indole and piperidine moieties suggests that it may interact with biological targets and exhibit therapeutic effects.
Used in Drug Discovery:
In the field of drug discovery, 1-(2,3-dihydro-1H-indol-1-yl)-3-(piperidin-1-yl)propan-1-one is used as a starting point for the development of new drugs. Its complex structure and the presence of biologically active moieties make it a promising candidate for further investigation and optimization to target specific diseases or conditions.
Used in Synthetic Organic Chemistry:
1-(2,3-dihydro-1H-indol-1-yl)-3-(piperidin-1-yl)propan-1-one is used as a building block in synthetic organic chemistry for the synthesis of other related chemical entities. Its unique structure and functional groups can be utilized to create a variety of novel compounds with potential applications in various industries, including pharmaceuticals, agrochemicals, and materials science.
Used in Medicinal Chemistry:
In medicinal chemistry, 1-(2,3-dihydro-1H-indol-1-yl)-3-(piperidin-1-yl)propan-1-one is used as a lead compound for the design and development of new therapeutic agents. Its complex structure and the presence of pharmacophore elements make it a valuable starting point for the creation of new drugs with improved efficacy, selectivity, and safety profiles.
Check Digit Verification of cas no
The CAS Registry Mumber 64140-56-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,1,4 and 0 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 64140-56:
(7*6)+(6*4)+(5*1)+(4*4)+(3*0)+(2*5)+(1*6)=103
103 % 10 = 3
So 64140-56-3 is a valid CAS Registry Number.