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1,7,13-Trioxa-4,10,16-triazacyclooctadecane-3,11-dione, 4,10-dimethyl-16-[(4-methylphenyl)sulfonyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

105206-48-2

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105206-48-2 Usage

Molecular structure

A complex organic molecule with a cyclic structure containing three oxygen atoms and three nitrogen atoms arranged in a specific pattern.

Functional groups

The compound has a 3,11-dione functional group, indicating the presence of a ketone moiety at these positions.

Additional groups

The molecule has methyl and sulfonyl groups attached at specific positions.

Sulfonamide compound

The presence of the sulfonyl group suggests that it is likely to be a sulfonamide compound.

Potential applications

The compound's intricate structure and diverse functional groups suggest it may have potential applications in various fields such as pharmaceuticals, materials science, or as a complexing agent in chemical processes.

Molecular weight

Approximately 429.58 g/mol

Stereochemistry

The compound may have stereoisomers due to the presence of chiral centers in the molecule.

Solubility

The compound's solubility properties are not explicitly mentioned, but it may be influenced by its polar and nonpolar functional groups.

Stability

The stability of the compound may depend on factors such as temperature, pH, and the presence of other reactive species.

Reactivity

The compound may undergo various chemical reactions due to the presence of its functional groups, such as nucleophilic addition, electrophilic substitution, or elimination reactions.

Synthesis

The synthesis of 1,7,13-Trioxa-4,10,16-triazacyclooctadecane-3,11-dione, 4,10-dimethyl-16-[(4-methylphenyl)sulfonyl]- may involve multiple steps, including the formation of the cyclic structure, introduction of functional groups, and subsequent modifications.

Analytical techniques

Techniques such as NMR, IR, and mass spectrometry can be used to analyze and confirm the structure of 1,7,13-Trioxa-4,10,16-triazacyclooctadecane-3,11-dione, 4,10-dimethyl-16-[(4-methylphenyl)sulfonyl]-.

Hazards

The compound's hazards, such as toxicity, flammability, or reactivity, are not explicitly mentioned but should be considered based on its functional groups and potential applications.

Storage and handling

Appropriate storage and handling conditions should be determined based on the compound's stability, reactivity, and potential hazards.

Check Digit Verification of cas no

The CAS Registry Mumber 105206-48-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,2,0 and 6 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 105206-48:
(8*1)+(7*0)+(6*5)+(5*2)+(4*0)+(3*6)+(2*4)+(1*8)=82
82 % 10 = 2
So 105206-48-2 is a valid CAS Registry Number.

105206-48-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-<(4-methylphenyl)sylfonyl>-7,13-dimethyl-1,7,13-triaza-4,10,16-trioxacyclooctadecane-6,14-dione

1.2 Other means of identification

Product number -
Other names 4,10-Dimethyl-16-(toluene-4-sulfonyl)-1,7,13-trioxa-4,10,16-triaza-cyclooctadecane-3,11-dione

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:105206-48-2 SDS

105206-48-2Relevant academic research and scientific papers

Tetazac: A Novel Artificial Receptor for Binding ω-Amino Carboxylates

Schmidtchen, F. P.

, p. 5161 - 5168 (2007/10/02)

Our concept to produce linearly connected polytopic artificial receptors was developed in order to enhance binding selectivity while conserving a reasonable synthesizability of the host compound.A first step in this direction involves the synthesis of Tet

SYNTHESIS OF AN ABIOTIC DITOPIC RECEPTOR MOLECULE

Schmidtchen, F.P.

, p. 4361 - 4364 (2007/10/02)

The synthesis of the ditopic host molecule 1 is described, which binds aminocarboxylates with preference over simple ammonium salts.

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