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(R,S)-N-benzyloxycarbonyl-4-(ethan-1'-amino)piperidine is a chiral piperidine derivative featuring a piperidine ring with an attached benzyloxycarbonyl group and an ethan-1'-amino group. (R,S)-N-benzyloxycarbonyl-4-(ethan-1'-amino)piperidine has both (R) and (S) configurations and is known for its potential applications in organic synthesis and pharmaceutical research, particularly in the development of new drugs and medication. The benzyloxycarbonyl group serves as a protecting group in organic chemistry, while the piperidine ring and the ethan-1'-amino group hint at possible biological activity and pharmacological relevance.

863560-19-4

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863560-19-4 Usage

Uses

Used in Organic Synthesis:
(R,S)-N-benzyloxycarbonyl-4-(ethan-1'-amino)piperidine is used as an intermediate in the synthesis of various organic compounds due to its unique structural features and reactivity.
Used in Pharmaceutical Research:
(R,S)-N-benzyloxycarbonyl-4-(ethan-1'-amino)piperidine is used as a key component in the development of new drugs and medication, leveraging its potential biological activity and pharmacological relevance for therapeutic applications.
Used in Drug Design and Medicinal Chemistry:
In the field of drug design and medicinal chemistry, (R,S)-N-benzyloxycarbonyl-4-(ethan-1'-amino)piperidine is used as a building block for creating novel molecular entities with potential therapeutic properties, taking advantage of its chiral nature and functional groups for further chemical modifications and optimizations.

Check Digit Verification of cas no

The CAS Registry Mumber 863560-19-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,3,5,6 and 0 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 863560-19:
(8*8)+(7*6)+(6*3)+(5*5)+(4*6)+(3*0)+(2*1)+(1*9)=184
184 % 10 = 4
So 863560-19-4 is a valid CAS Registry Number.

863560-19-4Relevant academic research and scientific papers

4-SUBSTITUTED PIPERIDINE DERIVATIVES

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Page/Page column 134, (2008/06/13)

Substituted piperidine compounds represented by the structure I are provided, wherein each of Rla, R1b, R1c, R1d, Rle, R1f, R1g, R1h, R2, R2A, R3, R4, A, X, a, x, and n is as defined in the specification. Substituted piperidine compounds of structure I may permeate or penetrate across a nerve cell membrane into the interior of a nerve cell, may inhibit intracellular Rho kinase enzyme found in nerve cells in mammals, and may find utility in repair of damaged nerves in the central and peripheral nervous system of such mammals. These compounds may induce the regeneration or growth of neurites in mammalian nerve cells and may thereby induce regeneration of damaged or diseased nerve tissue. These compounds also find additional utility as antagonists of the enzyme Rho kinase in treatment of disease states in which Rho kinase is implicated. Pharmaceutical compositions containing these substituted piperidine compounds may be useful to promote neurite growth and in the treatment of diseases in which Rho kinase inhibition is indicated.

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