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17348-66-2

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17348-66-2 Usage

General Description

T-butyldimethylIsopropoxylsilane is a chemical compound used in various industrial and research applications. It is a silane-based compound with the chemical formula C9H22OSi and a molecular weight of 174.36 g/mol. t-butyldimethylIsopropoxylsilane is a colorless liquid with a strong odor and is highly flammable. It is used as a coupling agent, crosslinking agent, and surface modifier in the production of adhesives, sealants, and coatings. T-butyldimethylIsopropoxylsilane is also utilized in the manufacturing of silicone polymers, ceramics, and electronic materials. It is important to handle this chemical with caution and follow proper safety protocols due to its flammability and potential health hazards.

Check Digit Verification of cas no

The CAS Registry Mumber 17348-66-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,3,4 and 8 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 17348-66:
(7*1)+(6*7)+(5*3)+(4*4)+(3*8)+(2*6)+(1*6)=122
122 % 10 = 2
So 17348-66-2 is a valid CAS Registry Number.

17348-66-2SDS

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 tert-butyl-dimethyl-propan-2-yloxysilane

1.2 Other means of identification

Product number -
Other names Isopropyloxy-dimethyl-tert-butyl-silan

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:17348-66-2 SDS

17348-66-2Downstream Products

17348-66-2Relevant articles and documents

Functionalized olefin cross-coupling to construct carbon-carbon bonds

Lo, Julian C.,Gui, Jinghan,Yabe, Yuki,Pan, Chung-Mao,Baran, Phil S.

, p. 343 - 348 (2015/03/04)

Carbon-carbon (C-C) bonds form the backbone of many important molecules, including polymers, dyes and pharmaceutical agents. The development of new methods to create these essential connections in a rapid and practical fashion has been the focus of numerous organic chemists. This endeavour relies heavily on the ability to form C-C bonds in the presence of sensitive functional groups and congested structural environments. Here we report a chemical transformation that allows the facile construction of highly substituted and uniquely functionalized C-C bonds. Using a simple iron catalyst, an inexpensive silane and a benign solvent under ambient atmosphere, heteroatom-substituted olefins are easily reacted with electron-deficient olefins to create molecular architectures that were previously difficult or impossible to access. More than 60 examples are presented with a wide array of substrates, demonstrating the chemoselectivity and mildness of this simple reaction.

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