401518-12-5 Usage
Chemical class
Piperidine class of organic compounds
Piperidine ring
A six-membered nitrogen-containing ring
BOC protecting group
tert-butoxycarbonyl group attached to the nitrogen atom
BOC protecting group
Protects the nitrogen atom during chemical reactions
Cyano group
A carbon triple-bonded to nitrogen (-CN) attached to the piperidine ring
Cyano group
Can participate in various chemical reactions, such as addition, substitution, and reduction
Methoxyphenyl group
A phenyl ring with a methoxy (-OCH3) substituent
Cyclopentyloxy group
A five-membered cycloalkane ring attached to the phenyl group via an oxygen atom
Cyclopentyloxy group
Can affect the compound's lipophilicity and steric properties
Potential applications
Medicinal and pharmaceutical chemistry
Drug development
Development of new drugs and molecules for various therapeutic purposes
Research and development
Unique structure and properties make it an interesting candidate for further research
Methoxy group
Can influence the compound's solubility, reactivity, and biological activity
Synthesis
The compound can be synthesized through various chemical reactions, such as nucleophilic substitution, addition, and cyclization reactions.
Stability
The compound's stability can be influenced by factors such as temperature, pH, and the presence of other reactive species.
Reactivity
The compound may undergo various chemical reactions, such as substitution, elimination, and rearrangement reactions, depending on the reaction conditions and the presence of other reactants.
Biological activity
The compound's biological activity can be influenced by its structure, functional groups, and interactions with biological targets, such as enzymes, receptors, and ion channels.
Safety and handling
As with any chemical compound, appropriate safety measures should be taken when handling 1-BOC-4-CYANO-4-[3-(CYCLOPENTYLOXY)-4-METHOXYPHENYL]-PIPERIDINE, including the use of personal protective equipment and proper disposal of waste materials.
Analytical techniques
The compound can be characterized and analyzed using various analytical techniques, such as nuclear magnetic resonance (NMR) spectroscopy, mass spectrometry, and infrared (IR) spectroscopy.
Check Digit Verification of cas no
The CAS Registry Mumber 401518-12-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,1,5,1 and 8 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 401518-12:
(8*4)+(7*0)+(6*1)+(5*5)+(4*1)+(3*8)+(2*1)+(1*2)=95
95 % 10 = 5
So 401518-12-5 is a valid CAS Registry Number.
401518-12-5Relevant articles and documents
Highly potent PDE4 inhibitors with therapeutic potential
Ochiai, Hiroshi,Ohtani, Tazumi,Ishida, Akiharu,Kusumi, Kensuke,Kato, Masashi,Kohno, Hiroshi,Odagaki, Yoshihiko,Kishikawa, Katuya,Yamamoto, Susumu,Takeda, Hiroshi,Obata, Takaaki,Nakai, Hisao,Toda, Masaaki
, p. 4645 - 4665 (2007/10/03)
Synthesis and biological evaluation of piperidine derivatives is reported. The hypothesis that the dose-limiting side effects of PDE4 inhibitors could be mediated via the central nervous system prompted us to design and synthesize a hydrophilic piperidine
Piperidine derivatives and drugs containing these derivatives as active ingredient
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Page/Page column 16, (2008/06/13)
Piperidine derivatives represented by formula (I) or nontoxic salts thereof (wherein symbols are defined in the description): Since the compound represented by formula (I) has a PDE4 inhibitory activity, it is useful for preventing and/or treating inflamm
