16310-38-6 Usage
Description
4-[(4-CHLOROPHENYL)SULFONYL]PIPERIDINE HYDROCHLORIDE is a hydrochloride salt form of a sulfonyl-substituted piperidine derivative, belonging to the class of piperidine compounds. It is a promising chemical compound with potential applications in various fields, including pharmaceuticals and medicinal chemistry.
Used in Pharmaceutical Industry:
4-[(4-CHLOROPHENYL)SULFONYL]PIPERIDINE HYDROCHLORIDE is used as a pharmaceutical intermediate for the synthesis of various organic compounds. Its unique chemical structure allows it to serve as a building block in the development of new drug candidates, contributing to the advancement of pharmaceutical research and drug discovery.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 4-[(4-CHLOROPHENYL)SULFONYL]PIPERIDINE HYDROCHLORIDE is utilized for the development of new drug candidates. Its sulfonyl-substituted piperidine structure offers potential therapeutic properties, making it a valuable component in the design and synthesis of novel pharmaceutical agents.
Safety Considerations:
Due to its potentially hazardous nature, it is crucial to handle 4-[(4-CHLOROPHENYL)SULFONYL]PIPERIDINE HYDROCHLORIDE with proper care and follow safety guidelines. This ensures the safety of individuals working with the compound and minimizes any potential risks associated with its use.
Check Digit Verification of cas no
The CAS Registry Mumber 16310-38-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,3,1 and 0 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 16310-38:
(7*1)+(6*6)+(5*3)+(4*1)+(3*0)+(2*3)+(1*8)=76
76 % 10 = 6
So 16310-38-6 is a valid CAS Registry Number.
InChI:InChI=1/C11H14ClNO2S.ClH/c12-9-1-3-10(4-2-9)16(14,15)11-5-7-13-8-6-11;/h1-4,11,13H,5-8H2;1H
16310-38-6Relevant articles and documents
TAUTOMERISM OF DERIVATIVES OF AZINES. 16. TAUTOMERISM OF ACYLMETHYLPYRAZINES AND -QUINOXALINES
Mainagashev, I. Ya.,Lapachev, V. V.,Fedotov, M. A.,Mamaev, V. P.
, p. 1339 - 1342 (2007/10/02)
The tautomeric equilibria of acylmethylpyrazines and -quinoxalines in chloroform were studied by 1H, 14N, and 17O NMR spectroscopy.It was shown that keto-enol tautomerism is realized in the acylmethylpyrazine series.Annelation leads to the development of an ylidene tautomer in the acylmethylquinoxaline series.A marked dependence of the position of the intrachelate equilibrium on the character of the solvent was observed.
Syntheses of 2-(2-Quinoxalyl)-1-phenylethanone and Related Ethanones
Sund, Eldon H.,Callender, David L.
, p. 189 (2007/10/02)
Nine 2-(2-quinoxalyl)-1-phenylethanones were synthesized by the condensation of 2-methylquinoxaline and the requisite methyl benzoate ester with sodium hydride as the condensing agent.Substituents in the 3 or 4 positions of the phenyl ring were methyl, methoxy, chloro, or trifluoromethyl.
