863560-23-0 Usage
Uses
Used in Pharmaceutical Synthesis:
(R,S)-4-[N'-(tert-butyloxycarbonyl)ethan-1'-amino]piperidine is used as an intermediate in the pharmaceutical industry for the synthesis of various drugs. The presence of the Boc group allows for selective protection of the amino group, enabling the compound to be a versatile building block in the development of new medications.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (R,S)-4-[N'-(tert-butyloxycarbonyl)ethan-1'-amino]piperidine serves as a valuable compound for the design and synthesis of novel bioactive molecules. Its structural features, including the piperidine ring and the protected amino group, make it a promising candidate for the creation of potential therapeutic agents.
Used in Organic Synthesis:
(R,S)-4-[N'-(tert-butyloxycarbonyl)ethan-1'-amino]piperidine is also utilized in organic synthesis as a key component in the assembly of complex organic molecules. The Boc group's protective nature allows chemists to carry out reactions selectively, facilitating the synthesis of a wide range of organic compounds with potential applications in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 863560-23-0 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, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 863560-23:
(8*8)+(7*6)+(6*3)+(5*5)+(4*6)+(3*0)+(2*2)+(1*3)=180
180 % 10 = 0
So 863560-23-0 is a valid CAS Registry Number.
863560-23-0Relevant academic research and scientific papers
4-SUBSTITUTED PIPERIDINE DERIVATIVES
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Page/Page column 136, (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.
