868245-27-6 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule. In this case, the compound has 12 carbon (C) atoms, 16 hydrogen (H) atoms, 2 nitrogen (N) atoms, and 1 oxygen (O) atom.
Explanation
This structure indicates the arrangement of atoms and the type of chemical bonds between them. The compound consists of a pyridine ring with a 3-pyridinyl group and a 6-(1-piperazinyl) group attached to it, and an ethanone (keto) group at the 1-position.
Explanation
The compound is derived from a ketone, specifically ethanone, with additional functional groups (pyridine and piperazine) attached to it.
Explanation
The compound's structural features, including the presence of a ketone, pyridine, and piperazine groups, make it a valuable component in the development of new chemical entities for diverse purposes.
Explanation
The specific properties and potential uses of 1-[6-(1-Piperazinyl)-3-pyridinyl]ethanone may vary depending on the context and application in which it is used, such as in the synthesis of pharmaceuticals or other organic compounds.
Chemical Structure
1-[6-(1-Piperazinyl)-3-pyridinyl]ethanone
Functional Groups
Ketone, Pyridine, and Piperazine
Type of Compound
Ketone Derivative
Applications
Research and Pharmaceutical
Structural Features
Valuable Component in Chemical Development
Potential Uses
Varies depending on context and application
Check Digit Verification of cas no
The CAS Registry Mumber 868245-27-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,8,2,4 and 5 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 868245-27:
(8*8)+(7*6)+(6*8)+(5*2)+(4*4)+(3*5)+(2*2)+(1*7)=206
206 % 10 = 6
So 868245-27-6 is a valid CAS Registry Number.
InChI:InChI=1/C11H15N3O/c1-9(15)10-2-3-11(13-8-10)14-6-4-12-5-7-14/h2-3,8,12H,4-7H2,1H3
868245-27-6Relevant articles and documents
Pd-Catalyzed Synthesis of Piperazine Scaffolds under Aerobic and Solvent-Free Conditions
Reilly, Sean W.,Mach, Robert H.
supporting information, p. 5272 - 5275 (2016/10/31)
A facile Pd-catalyzed methodology providing an efficient synthetic route to biologically relevant arylpiperazines under aerobic conditions is reported. Electron donating and sterically hindered aryl chlorides were aminated to afford yields up to 97%, with examples using piperazine as solvent, illustrating an ecofriendly, cost-effective synthesis of these privileged structures.
ACYLATED PIPERIDIHES AS GLYCINE TRANSPORTER INHIBITORS
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Page/Page column 61, (2010/11/23)
The invention provides a compound of formula (I) or a salt or solvate thereof: wherein R1, n, X, Y and Z are as defined in the specification, and uses of such compounds. The compounds inhibit GlyT1 transporters and are useful in the treatment of certain neurological and neuropsychiatric disorders, including schizophrenia.
PIPERAZINE DERIVATIVES AS GLYT1 INHIBITORS
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Page/Page column 51, (2010/11/23)
The invention provides a compound of formula (I) or a salt or solvate thereof: wherein R1, n, X, Y and Z are as defined in the specification, and uses of such compounds. The compounds inhibit GlyT1 transporters and are useful in the treatment of certain neurological and neuropsychiatric disorders, including schizophrenia.
