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N-[(2,4,6-trimethylphenyl)sulfonyl]tricyclo[3.3.1.1~3,7~]decane-1-carboxamide is a complex organic compound with the molecular formula C21H27NO2S. It is characterized by a tricyclic decane core, with a carboxamide group attached to the first carbon atom of the decane ring. The sulfonyl group is derived from 2,4,6-trimethylphenol, which is attached to the nitrogen atom of the carboxamide. This chemical is known for its potential applications in pharmaceuticals, particularly as a precursor in the synthesis of certain drugs. Its structure provides it with unique properties that can be exploited in medicinal chemistry, although specific details about its pharmacological activity or therapeutic use are not provided in this summary.

5582-59-2

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5582-59-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5582-59-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,5,8 and 2 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5582-59:
(6*5)+(5*5)+(4*8)+(3*2)+(2*5)+(1*9)=112
112 % 10 = 2
So 5582-59-2 is a valid CAS Registry Number.

5582-59-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(2,4,6-trimethylphenyl)sulfonyladamantane-1-carboxamide

1.2 Other means of identification

Product number -
Other names Tetraphenylcyclotetraarsthian

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:5582-59-2 SDS

5582-59-2Downstream Products

5582-59-2Relevant academic research and scientific papers

Thioacylsulfanylarsines (RCS2)xAsPh3-x, x = 1-3: Synthesis, structures, natural bond order analyses and reactions with piperidine

Tani, Kazuyasu,Hanabusa, Shin-Ichi,Kato, Shinzi,Mutoh, Shin-Ya,Suzuki, Shun-Ichi,Ishida, Masaru

, p. 518 - 527 (2007/10/03)

A series of thioacylsulfanylarsines ((RCS2)AsPh2, (RCS2)2AsPh, (RCS2)3As) were synthesized by treating piperidinium dithiocarboxylates with Ph2AsCl, PhAsCl2 or AsCl3, respectively and characterized. Their molecular structures were determined by X-ray crystallography and compared with those of the corresponding acylsulfanyl derivatives ((RCOS)AsPh2, (RCOS)2AsPh, (RCOS)3As). They exist as monomers, and the environment around the arsenic atoms is distorted tetrahedral with one lone pair at the apex. The structure of the mono(dithiocarboxylate) is different from that of the corresponding thiocarboxylic acid derivative, while the bis and tris derivatives showed similar structure to the corresponding thiocarboxylic acid derivatives ((RCOS)2AsPh, (RCOS)3As), respectively. The new compounds showed intramolecular interactions between the thiocarbonyl sulfur and the central arsenic atom. NBO (Natural Bond Orbital) analyses performed on the model compounds (CH3CS2)As(CH3)2 and (CH3CS21)-(CH3CS22 )AsCH3 at the RHF/LANL2DZ level of theory showed the presence of interactions between the non-bonding orbitals on the thiocarbonyl sulfur (ns) and the σ*MS orbitals together with that between the ns and the σ*MC orbitals for the former compound; for the latter the presence of both orbital interactions between ns and σ*MS1 and between ns and σ*MS2 are present. The reaction of the mono(dithiocarboxylate) derivative (R = 4-CH3-C6H4) with piperidine in ethanol gave piperidinium diphenyldithioarsinate along with the corresponding N-thioacyl- or N-acyl-piperidine. A similar reaction of the bis(dithiocarboxylate) derivative (R = 4-CH3C6H4) gave the novel di(piperidinium) phenyltrithioarsonate in which two anion charges are delocalized on the AsS3 moiety and a cyclic phenylarsine sulfide tetramer (PhAsS)4. The diphenyldithioarsinate and phenyltrithioarsonate salts exist as a dimer and a polymer, respectively, in which 12-membered rings are formed by intermolecular N-H ... S hydrogen bonds.

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