78058-42-1 Usage
Description
(S)-Piperidine-2-carboxamide hydrochloride is a chemical compound that serves as an intermediate in the pharmaceutical industry for the synthesis of various drugs. It is a salt form of piperidine-2-carboxamide, which is derived from piperidine—a six-membered heterocyclic ring structure. (S)-Piperidine-2-carboxamide hydrochloride is favored in pharmaceutical applications due to its stability and solubility properties.
Uses
Used in Pharmaceutical Industry:
(S)-Piperidine-2-carboxamide hydrochloride is used as a key intermediate for the synthesis of various medications, particularly in the development of antiviral and anticancer drugs. Its role in drug synthesis is crucial due to its ability to form complex organic molecules, which contribute to the effectiveness of these medications.
Used in Synthesis of Complex Organic Molecules:
In the field of organic chemistry, (S)-Piperidine-2-carboxamide hydrochloride is used as a building block for the synthesis of other complex organic molecules. Its structural properties make it a valuable component in creating a wide range of compounds with diverse applications.
Check Digit Verification of cas no
The CAS Registry Mumber 78058-42-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,0,5 and 8 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 78058-42:
(7*7)+(6*8)+(5*0)+(4*5)+(3*8)+(2*4)+(1*2)=151
151 % 10 = 1
So 78058-42-1 is a valid CAS Registry Number.
78058-42-1Relevant articles and documents
THERAPEUTIC COMPOUNDS: PYRIDINE AS SCAFFOLD
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Page/Page column 105, (2010/02/14)
Compounds of formulas I, IA, and IB or IC or pharmaceutically acceptable salts thereof: wherein A, A1, A2, A3, A4, R2, R3, R4 and n are as defined in the specifications well as salts and pharmaceutical compositions including the compounds are prepared. They are useful in therapy, in particular in the management of pain.
Dopamine Receptor Modulation by Pro-Leu-Gly-NH2 Analogues Possessing Cyclic Amino Acid Residues at the C-Terminal Position
Johnson, Rodney L.,Rajakumar, G.,Mishra, Ram K.
, p. 2100 - 2104 (2007/10/02)
The synthesis of several analogues of L-prolyl-L-leucylglycinamide (PLG) was carried out in which the glycinamide residue was replaced with the following cyclic amino acid residues: L- and D-prolinamide, (+)- and (-)-thiazolidine-2-carboxamide, L- and D-3
Tripeptides acting on the central nervous system and a process for the preparation thereof
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, (2008/06/13)
The invention relates to new peptide derivatives which act on the central nervous system and correspond to the general formula (I), wherein X is L-norleucyl, L-leucyl, L-norvalyl, D-leucyl, L-prolyl, L-2-aminobutyryl, L-valyl, L-threonyl, L-isoleu
