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35692-27-4

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35692-27-4 Usage

General Description

4-Methoxyphenyltrimethoxysilane is a chemical compound often used in pharmaceutical and organic synthesis processes. Its chemical formula is C10H14O4Si, indicative of the presence of carbon, hydrogen, oxygen, and silicon elements in it. It is a member of the silane family, typically in liquid form, with a slightly pungent smell. This chemical is used for a diverse range of applications including surface treatment, adhesive promotion, and chemical binding, due to its ability to form strong bonds with many surfaces. Its stability and reactivity depend on storage and handling conditions and precautions need to be taken while handling this chemical.

Check Digit Verification of cas no

The CAS Registry Mumber 35692-27-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,6,9 and 2 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 35692-27:
(7*3)+(6*5)+(5*6)+(4*9)+(3*2)+(2*2)+(1*7)=134
134 % 10 = 4
So 35692-27-4 is a valid CAS Registry Number.
InChI:InChI=1/C10H16O4Si/c1-11-9-5-7-10(8-6-9)15(12-2,13-3)14-4/h5-8H,1-4H3

35692-27-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name trimethoxy-(4-methoxyphenyl)silane

1.2 Other means of identification

Product number -
Other names 4-anisolyl trimethoxysilane

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:35692-27-4 SDS

35692-27-4Relevant articles and documents

Carbon-Silicon Bond Formation in the Synthesis of Benzylic Silanes

Visco, Michael D.,Wieting, Joshua M.,Mattson, Anita E.

supporting information, p. 2883 - 2885 (2016/07/06)

Sterically encumbered organosilanes can be difficult to synthesize with conventional, strongly basic reagents; the harsh reaction conditions are often low yielding and not suitable for many functional groups. As an alternative to the typical anionic strat

Copper-promoted C-N bond cross-coupling with hypervalent aryl siloxanes and room-temperature N-arylation with aryl iodide [5]

Lam, Patrick Y. S.,Deudon, Sophie,Averill, Kristin M.,Li, Renhua,He, Ming Y.,DeShong, Philip,Clark, Charles G.

, p. 7600 - 7601 (2007/10/03)

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