82360-26-7 Usage
General Description
4-(2-oxopiperidin-1-yl)butanoic acid, also known as 4-(2-oxopyrrolidin-1-yl)butanoic acid, is a chemical compound with the molecular formula C9H15NO3. It is a synthetic intermediate used in the production of pharmaceuticals, specifically in the development of drugs with potential anti-inflammatory and analgesic properties. 4-(2-oxopiperidin-1-yl)butanoic acid is a derivative of piperidine and butanoic acid, and its structural features make it a useful building block in organic synthesis. Its unique molecular structure and properties make it a valuable tool in drug discovery and development processes. Additionally, it may have potential applications in medicinal chemistry and biochemistry research.
Check Digit Verification of cas no
The CAS Registry Mumber 82360-26-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,3,6 and 0 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 82360-26:
(7*8)+(6*2)+(5*3)+(4*6)+(3*0)+(2*2)+(1*6)=117
117 % 10 = 7
So 82360-26-7 is a valid CAS Registry Number.
InChI:InChI=1/C9H15NO3/c11-8-4-1-2-6-10(8)7-3-5-9(12)13/h1-7H2,(H,12,13)
82360-26-7Relevant articles and documents
Intramolecular hydrogen bonding in derivatives of beta-alanine and gamma-amino butyric acid: Model studies for the folding of unnatural polypeptide backbones
Dado,Gellman
, p. 1054 - 1062 (2007/10/02)
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AZAPROPELLANES AS PHASE-TRANSFER CATALYSTS-II A CMR AND PMR STUDY OF THE THREE-DIMENSIONAL STRUCTURE OF 1-AZONIAPROPELLANES CONTAINING 5- AND 6-MEMBERED RINGS
McIntosh, John M.
, p. 261 - 266 (2007/10/02)
An improved synthesis of 1-azoniatricyclo1,6>tridecane (2) and the preparation of the remaining member of the series, 1-azoniatricyclo1,6>dodecane salts (3) have been achieved.Using a combination of 1H (at 400 MHz) and 13C NMR spectra has allowed the assignment of the signals in the well-resolved 1H spectra.The results indicate that 1 exists in the all-chair form which undergoes racemisation by ring inversion with a rate constant of 0.7 sec-1 and further that the counterion in these salts is restricted to associating with only one face of the tetrahedral N atom.
