16310-38-6 Usage
General Description
4-[(4-Chlorophenyl)sulfonyl]piperidine hydrochloride is a chemical compound that belongs to the class of piperidine compounds. It is a hydrochloride salt form of 4-[(4-chlorophenyl)sulfonyl]piperidine, which is a sulfonyl-substituted piperidine derivative. 4-[(4-CHLOROPHENYL)SULFONYL]PIPERIDINE HYDROCHLORIDE has potential use as a pharmaceutical intermediate or building block in the synthesis of various organic compounds. It may also have potential applications in medicinal chemistry for the development of new drug candidates. Additionally, it is important to handle this chemical with proper care and follow safety guidelines due to its potentially hazardous nature.
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.
