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(1-benzoyl-4-phenylpiperidine-4-yl)acetaldehyde is a complex chemical compound that features a benzoyl group, a phenyl group, and a piperidine ring, along with an aldehyde functional group. Its intricate structure suggests potential applications in organic synthesis and medicinal chemistry, given the prevalence of benzoyl and piperidine groups in pharmaceuticals and bioactive molecules.

716358-36-0

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716358-36-0 Usage

Uses

Used in Organic Synthesis:
(1-benzoyl-4-phenylpiperidine-4-yl)acetaldehyde is used as a key intermediate in the synthesis of various organic compounds due to its reactive aldehyde group and the presence of multiple functional groups that can participate in a range of chemical reactions.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (1-benzoyl-4-phenylpiperidine-4-yl)acetaldehyde is used as a building block for the development of new pharmaceuticals, leveraging the bioactivity often associated with benzoyl and piperidine-containing molecules.
Further research and characterization are essential to explore the full potential of (1-benzoyl-4-phenylpiperidine-4-yl)acetaldehyde and to understand its properties and possible applications more comprehensively.

Check Digit Verification of cas no

The CAS Registry Mumber 716358-36-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,1,6,3,5 and 8 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 716358-36:
(8*7)+(7*1)+(6*6)+(5*3)+(4*5)+(3*8)+(2*3)+(1*6)=170
170 % 10 = 0
So 716358-36-0 is a valid CAS Registry Number.

716358-36-0Downstream Products

716358-36-0Relevant academic research and scientific papers

Discovery of bioavailable 4,4-disubstituted piperidines as potent ligands of the chemokine receptor 5 and inhibitors of the human immunodeficiency virus-1

Kazmierski, Wieslaw M.,Aquino, Christopher,Chauder, Brian A.,Deanda, Felix,Ferris, Robert,Jones-Hertzog, Deborah K.,Kenakin, Terrence,Koble, Cecilia S.,Watson, Christian,Wheelan, Pat,Yang, Hanbiao,Youngman, Michael

experimental part, p. 6538 - 6546 (2009/11/30)

We describe robust chemical approaches toward putative CCR5 scaffolds designed in our laboratories. Evaluation of analogues in the 125I-[MIP-1β] binding and Ba-L-HOS antiviral assays resulted in the discovery of 64 and 68 in the 4,4-disubstitited piperidine class H, both potent CCR5 ligands (pIC50 = 8.30 and 9.00, respectively) and HIV-1 inhibitors (pIC50 = 7.80 and 7.84, respectively, in Ba-L-HOS assay). In addition, 64 and 68 were bioavailable in rodents, establishing them as lead molecules for further optimization toward CCR5 clinical candidates.

CCR5 ANTAGONISTS AS THERAPEUTIC AGENTS

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Page 50 - 51, (2010/02/07)

The present invention relates to compounds of formula (I) or pharmaceutically acceptable derivatives thereof, useful in the treatment or prophylaxis of CCR5-related diseases and disorders, for example, in the inhibition of HIV replication, the prevention or treatment of an HIV infection, and in the treatment of the resulting acquired immune deficiency syndrome (AIDS).

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