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1825-65-6

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1825-65-6 Usage

General Description

Butoxytrimethylsilane is an organosilicon compound with the chemical formula C7H18OSi. It is a clear, colorless liquid that is soluble in organic solvents but insoluble in water. Butoxytrimethylsilane is commonly used as a coupling agent in the synthesis of organic and inorganic substances, as well as in the production of silicone polymers and resins. It is also utilized as a chemical intermediate in the manufacturing of adhesives, sealants, and surface modifiers. Additionally, butoxytrimethylsilane is a key component in the formulation of coatings, paints, and printing inks for its ability to enhance adhesion and water repellency. However, it is important to handle this chemical with caution due to its flammability and potential for causing skin and eye irritation.

Check Digit Verification of cas no

The CAS Registry Mumber 1825-65-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,2 and 5 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1825-65:
(6*1)+(5*8)+(4*2)+(3*5)+(2*6)+(1*5)=86
86 % 10 = 6
So 1825-65-6 is a valid CAS Registry Number.
InChI:InChI=1/C7H18OSi/c1-5-6-7-8-9(2,3)4/h5-7H2,1-4H3

1825-65-6SDS

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 butoxy(trimethyl)silane

1.2 Other means of identification

Product number -
Other names trimethyl-n-butoxysilane

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:1825-65-6 SDS

1825-65-6Relevant articles and documents

Molybdenum-catalyzed transformation of molecular dinitrogen into silylamine: Experimental and DFT study on the remarkable role of ferrocenyldiphosphine ligands

Tanaka, Hiromasa,Sasada, Akira,Kouno, Tomohisa,Yuki, Masahiro,Miyake, Yoshihiro,Nakanishi, Haruyuki,Nishibayashi, Yoshiaki,Yoshizawa, Kazunari

supporting information; experimental part, p. 3498 - 3506 (2011/05/04)

A molybdenum-dinitrogen complex bearing two ancillary ferrocenyldiphosphine ligands, trans-[Mo(N2)2(depf)2] (depf = 1,1′-bis(diethylphosphino)ferrocene), catalyzes the conversion of molecular dinitrogen (N2) into silylamine (N(SiMe3) 3), which can be readily converted into NH3 by acid treatment. The conversion has been achieved in the presence of Me 3SiCl and Na at room temperature with a turnover number (TON) of 226 for the N(SiMe3)3 generation for 200 h. This TON is significantly improved relative to those ever reported by Hidai's group for mononuclear molybdenum complexes having monophosphine coligands [J. Am. Chem. Soc.1989, 111, 1939]. Density functional theory (DFT) calculations have been performed to figure out the mechanism of the catalytic N2 conversion. On the basis of some pieces of experimental information, SiMe3 radical is assumed to serve as an active species in the catalytic cycle. Calculated results also support that SiMe3 radical is capable of working as an active species. The formation of five-coordinate intermediates, in which one of the N2 ligands or one of the Mo-P bonds is dissociated, is essential in an early stage of the N2 conversion. The SiMe 3 addition to a "hydrazido(2-)" intermediate having the NN(SiMe3)2 group will give a "hydrazido(1-)" intermediate having the (Me3Si)NN(SiMe3)2 group rather than a pair of a nitrido (-N) intermediate and N(SiMe3) 3. The N(SiMe3)3 generation would not occur at the Mo center but proceed after the (Me3Si)NN(SiMe3) 2 group is released from the Mo center. The flexibility of the Mo-P bond between Mo and depf would play a vital role in the high catalysis of the Mo-Fe complex.

Reactions of Acetophenone Dibutyl Acetal with Dipropylchloroborane and Trimethylchlorosilane

Bagdasaryan, G. B.,Sarkisova, E. A.,Indzhikyan, M. G.

, p. 354 - 356 (2007/10/03)

Acetophenone dibutyl acetal reacts with dipropylchloroborane or trimethylchlorosilane, yielding 1,3,5-triphenylbenzene.The reaction is also successful in the presence of catalytic amounts of these electrophiles.

REACTION OF OCTAMETHYLTRISILOXANE WITH 2-ALKOXY-1,3-DIOXACYCLOALKANES

Nedogrei, E. P.,Zhurkina, I. P.,Musavirov, R. S.,Rakhmankulov, D. L.,Syrkin, A. M.

, p. 2231 - 2234 (2007/10/02)

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