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18276-53-4

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18276-53-4 Usage

General Description

Trimethylsilylpyrazole is a chemical compound with the molecular formula C8H14N2Si. It is a pyrazole derivative with three methyl groups and one trimethylsilyl group attached to the nitrogen atom of the pyrazole ring. Trimethylsilylpyrazole is commonly used in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds. It is also employed as a ligand in organometallic chemistry, where it can coordinate with transition metals to form stable complexes. Additionally, trimethylsilylpyrazole has been studied for its potential applications in materials science, such as in the development of advanced polymers and functionalized surfaces. Overall, trimethylsilylpyrazole has diverse uses in organic synthesis and materials research, making it an important compound in the field of chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 18276-53-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,2,7 and 6 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 18276-53:
(7*1)+(6*8)+(5*2)+(4*7)+(3*6)+(2*5)+(1*3)=124
124 % 10 = 4
So 18276-53-4 is a valid CAS Registry Number.
InChI:InChI=1/C13H28Cl2Si/c1-3-4-5-6-7-8-9-10-11-12-13-16(2,14)15/h3-13H2,1-2H3

18276-53-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name TRIMETHYLSILYLPYRAZOLE

1.2 Other means of identification

Product number -
Other names trimethyl-pyrrol-1-yl-silane

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:18276-53-4 SDS

18276-53-4Relevant articles and documents

A Simple Synthesis of Phenanthrene

Allen, Robert W.,Gilbertson, Jeffrey J.,Gribble, Gordon W.

, (2020)

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Frisch,Kary

, p. 931 (1956)

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Nagy et al.

, p. 293,295 - 297, 300, 302 (1969)

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Palladium catalysed aryl amination reactions in supercritical carbon dioxide

Smith, Catherine J.,Tsang, Melanie W.S.,Holmes, Andrew B.,Danheiser, Rick L.,Tester, Jefferson W.

, p. 3767 - 3781 (2007/10/03)

Palladium catalysed C-N bond formation in supercritical carbon dioxide has been accomplished. Carbamic acid formation is avoided in part through the use of an N-silylamine as the coupling partner. Employing a catalyst system of Pd 2dba3 (1 mol%) and 2-dicyclohexylphosphino-2′, 4′,6′-triisopropyl-1,1′-biphenyl (X-Phos) (2 mol%) enabled the catalytic amination of aryl bromides and chlorides with N-silylanilines to be realised in excellent yield. Extension of the methodology to the N-arylation of N-silyldiarylamines, N-silylazoles and N-silylsulfonamides is reported. The Royal Society of Chemistry 2005.

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