69001-10-1 Usage
General Description
Ethyl 1-acetylpiperidine-4-carboxylate is a chemical compound with the molecular formula C12H19NO3. It is a derivative of piperidine, a heterocyclic organic compound, and contains an acetyl group and an ethyl ester group. ethyl 1-acetylpiperidine-4-carboxylate is commonly used in organic synthesis and pharmaceutical research, where it can be utilized as an intermediate or building block in the synthesis of various pharmaceutical drugs and other organic compounds. Ethyl 1-acetylpiperidine-4-carboxylate may also have potential applications in medicinal chemistry and drug development due to its structural and pharmacological properties. Additionally, it is important to handle this compound with caution, as it may present certain hazards and risks if not properly handled and stored.
Check Digit Verification of cas no
The CAS Registry Mumber 69001-10-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,0,0 and 1 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 69001-10:
(7*6)+(6*9)+(5*0)+(4*0)+(3*1)+(2*1)+(1*0)=101
101 % 10 = 1
So 69001-10-1 is a valid CAS Registry Number.
InChI:InChI=1/C10H17NO3/c1-3-14-10(13)9-4-6-11(7-5-9)8(2)12/h9H,3-7H2,1-2H3
69001-10-1Relevant articles and documents
Concurrent esterification and N-acetylation of amino acids with orthoesters: A useful reaction with interesting mechanistic implications
Gibson, Sarah,Romero, Dickie,Jacobs, Hollie K.,Gopalan, Aravamudan S.
scheme or table, p. 6737 - 6740 (2011/02/25)
The concurrent esterification and N-acetylation of amino acids has been studied with triethyl orthoacetate (TEOA) and triethyl orthoformate (TEOF). In a surprising finding, only 1 equiv of TEOA in refluxing toluene was necessary to convert l-proline and l-phenylalanine into the corresponding N-acetyl ethyl esters in good yield. The same transformation using TEOF was not effective. Stereochemical outcome and stoichiometric studies as well as structural variation of the amino acids in this reaction provided unexpected mechanistic insight.
Process for making substituted pyrazoles
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Page 40-41, (2008/06/13)
This invention is directed generally to a process for making substituted pyrazoles, tautomers of the substituted pyrazoles, and salts of the substituted pyrazoles and tautomers. The substituted pyrazoles correspond in structure to Formula (I): wherein R3A, R3B, R3C, Y1, Y2, Y3, Y4, and Y5 are as defined in the specification.
