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6202-48-8

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6202-48-8 Usage

General Description

(1-Naphthyloxy)trimethylsilane is a chemical compound with the molecular formula C13H16OSi. It is a silane compound containing a trimethylsilyl group and a naphthoxy group. This chemical is commonly used as a reagent in organic synthesis, particularly in the functionalization of organic molecules. It can also be used as a protecting group for alcohols and phenols in organic chemistry reactions. Additionally, (1-Naphthyloxy)trimethylsilane has applications in the production of various pharmaceuticals and agrochemicals. Overall, it is a versatile chemical compound with important applications in organic synthesis and chemical manufacturing.

Check Digit Verification of cas no

The CAS Registry Mumber 6202-48-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,0 and 2 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6202-48:
(6*6)+(5*2)+(4*0)+(3*2)+(2*4)+(1*8)=68
68 % 10 = 8
So 6202-48-8 is a valid CAS Registry Number.

6202-48-8SDS

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 trimethyl(naphthalen-1-yloxy)silane

1.2 Other means of identification

Product number -
Other names Silane,trimethyl(1-naphthyloxy)

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:6202-48-8 SDS

6202-48-8Relevant articles and documents

Electrochemically driven desaturation of carbonyl compounds

Gnaim, Samer,Takahira, Yusuke,Wilke, Henrik R.,Yao, Zhen,Li, Jinjun,Delbrayelle, Dominique,Echeverria, Pierre-Georges,Vantourout, Julien C.,Baran, Phil S.

, p. 367 - 372 (2021/03/31)

Electrochemical techniques have long been heralded for their innate sustainability as efficient methods to achieve redox reactions. Carbonyl desaturation, as a fundamental organic oxidation, is an oft-employed transformation to unlock adjacent reactivity through the formal removal of two hydrogen atoms. To date, the most reliable methods to achieve this seemingly trivial reaction rely on transition metals (Pd or Cu) or stoichiometric reagents based on I, Br, Se or S. Here we report an operationally simple pathway to access such structures from enol silanes and phosphates using electrons as the primary reagent. This electrochemically driven desaturation exhibits a broad scope across an array of carbonyl derivatives, is easily scalable (1–100 g) and can be predictably implemented into synthetic pathways using experimentally or computationally derived NMR shifts. Systematic comparisons to state-of-the-art techniques reveal that this method can uniquely desaturate a wide array of carbonyl groups. Mechanistic interrogation suggests a radical-based reaction pathway. [Figure not available: see fulltext.]

Application of a novel nano-immobilization of ionic liquid on an MCM-41 system for trimethylsilylation of alcohols and phenols with hexamethyldisilazane

Zolfigol, Mohammad Ali,Sajjadifar, Sami,Ghorbani-Choghamarani, Arash,Tami, Farzaneh

, p. 7093 - 7106 (2018/08/17)

3-[(3-(Trisilyloxy)propyl)chloride]-1-methylimidazolium tribromide ionic liquid supported on MCM-41 [nano-MCM-41@(CH2)3-1-methylimidazole]Br3 as a novel heterogeneous nano-catalyst was easily prepared and characterized usi

Nano Fe3O4@ZrO2/SO42?: A highly efficient catalyst for the protection and deprotection of hydroxyl groups using HMDS under solvent-free condition

Ghafuri, Hossein,Paravand, Fatemeh,Rashidizadeh, Afsaneh

supporting information, p. 129 - 135 (2016/12/24)

In this work, we introduce a new procedure for the protection and deprotection process of various types of alcohols and phenols by HMDS in the presence of nano magnetic sulfated zirconia (Fe3O4@ZrO2/SO42?) as a solid acid catalyst under very mild and solvent-free condition. This method has interesting advantages like short reaction times and a simple workup process. With regard to some outstanding benefits of this new heterogeneous catalyst such as excellent yield, reusability of the catalyst and easy thermal stability, high acidity, strong and excellent magnetic properties, this method can be very interesting in aspect of green chemistry Principles.

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