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CAS:19241-16-8 | 2,6-DIMETHYLPHENYL ISOTHIOCYANATE

CAS:19241-16-8 | 2,6-DIMETHYLPHENYL ISOTHIOCYANATE

Molecular Formula:C9H9NS
Molecular Weigh:163.24
EINECS:242-906-0
Package:100g 1kg 5kg
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Made in China

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Product Introduction

Introduction of CAS:19241-16-8 | 2,6-DIMETHYLPHENYL ISOTHIOCYANATE

 

The molecular structure of compounds with the 2,6-dimethylphenyl group is often determined using X-ray crystallography. For example, the solid-state structures of phosphinamine chalcogenides and a zirconium complex were established by single-crystal X-ray diffraction analysis . The crystal and molecular-electronic structure of sterically hindered isomeric forms of dimethyl[methyl(phenylsulfonyl)amino]benzenesulfonyl chloride were also characterized by X-ray single-crystal diffraction .

 

Specification of CAS:19241-16-8 | 2,6-DIMETHYLPHENYL ISOTHIOCYANATE

 

ITEMS

SPECIFICATION

Boiling point

247 °C (lit.)

Density

1.085 g/mL at 25 °C (lit.)

Refractive index

n20/D 1.627(lit.)

Flash point

>230 °F

Storage condition

2 - 8°C

 

Research Application of CAS:19241-16-8 | 2,6-DIMETHYLPHENYL ISOTHIOCYANATE

 

Reactivity with Metal Complexes

It is used to study the reactivity of di(azido)bis(phosphine) complexes of Group 10 metals toward organic isothiocyanates, leading to the synthesis of various metal complexes (Kim et al., 2003).

Nanocrystal Growth Studies

Utilized as a molecular probe in studying the heterogeneous nucleation and growth of nanocrystals. This involves tracking the deposition of Pd on Ag nanocubes with surface-enhanced Raman scattering (Wu & Qin, 2018).

Organometallic Chemistry

The reaction of 2,6-Dimethylphenyl isocyanide with other compounds has been explored to study the behavior and structure of organometallic compounds (Klerks et al., 1981).

Photolysis Studies

Used in studies to understand the photolysis of related compounds and the formation of different molecular structures under specific conditions (Dunkin et al., 1985).

Dimerization and Molecular Structure Analysis

Used in the dimerization of isocyanides and in studying molecular structures, as seen in the formation of specific compounds like N,N′-Bis(2,6-dimethylphenyl)-2-methyl-1-(trimethylsilyl)ethane-1,2-diimine (Loroño-González, 2006).

Reactivity with Rhenium(V) Oxo Imido Complexes

Explored for its diverse reactivity with Rhenium(V) oxo imido complexes, which is crucial for developing new rhenium coordination complexes (Lohrey et al., 2020).

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