Information on Dimethylphenylsilanol

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dimethylphenylsilanol

Detailed information on Ethyl(dimethyl)phenylsilanol structure can be obtained by downloading its Structure data file. This file will give you information on its atoms, bond structures, connectivity, and more. Moreover, you can also view its Reactions, Structure data, and InChIKey. All these data will help you in understanding the chemical structure of this compound.

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Chemical structure

The molecular formula of dimethylphenylsilanol (3S)-3-ethoxyhexane identifies the various constituent elements by chemical symbols and tells us the proportionate number of atoms in each. The molecular weight of the compound is calculated by adding the atomic weights of each element to the total molecule’s molecular mass. Once calculated, the molecular weight is the mass of the compound in g/mol.

The molecule is a simple example of a ring of molecules. Its chemical structure refers to the arrangement of atoms and their chemical bonds. The molecule is made up of 26 atoms, each containing a hydrogen atom and one oxygen atom. Each atom is connected by a series of bonds called carbon atoms, hydrogen atoms, nitrogen atoms, and oxygen ions.

Reactions

The silanol reaction is governed by the pKa of the solvent as well as the pH in the mobile phase as well as the Ionic force that the column has. Silanol activity is typically determined at lower pH which is when the peaks become stronger. Silanols aren’t insoluble within water, making them an excellent option as organic chromatography.

To convert the silane to dimethylphenylsilane, the prochiral sila-ketone acetyldimethyl-(phenyl)silane was reduced to (R)-2 by a biocatalyst. The reaction was carried out on a size of 2.0 grams in a 5-1/ bioreactor. The conversion rate was between 45 and 55 mg (R)-2*min-1 and the entire substrates were converted within 1 hour of incubation.

Structure data

The chemical structure of dimethyl(phenyl)silane is available for download. This data file contains information on the atoms, bond structures, connectivity, coordinates, and more. You can rotate the dimethyl(phenyl)silane molecule interactively. And You can also zoom in or out by scrolling the mouse wheel. You can also view the structure of this compound by viewing the visualization.

A Dimethylphenylsilanola-derived molecule is available in the form of a structure data file. This file contains the exact coordinates, atoms, and bonds of the substance. It can be imported into most chemistry-related software packages. The atoms and bonding properties of a molecule are important for computational chemistry. However, this information is not always available for every molecule.

InChIKey

Standard InChIKeys are generated for each species in a participant VAMDC node. The format is based on the SHA-1 hash and the structure of a species must be translated to an InChI(Key). Openbabel and SMILES are programs that can do this. The format of the species must be in the same format as the original one, and it is not recommended that you use a beta version.

Version 1.03 of InChI was released in January 2009. This version does not produce duplicate structures and does not recognize potential tautomers. The generated InChIKeys are stored in a file for further analysis using PowerGREP software. The InChIKeys are stored in CML format. This format allows you to compare two InChIs without the need to generate a new one.