Welcome to LookChem.com Sign In|Join Free
  • or
Silane, trimethoxy[(phenylthio)methyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

57557-71-8

Post Buying Request

57557-71-8 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

57557-71-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 57557-71-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,5,5 and 7 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 57557-71:
(7*5)+(6*7)+(5*5)+(4*5)+(3*7)+(2*7)+(1*1)=158
158 % 10 = 8
So 57557-71-8 is a valid CAS Registry Number.

57557-71-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name trimethoxy(phenylsulfanylmethyl)silane

1.2 Other means of identification

Product number -
Other names trimethoxy-phenylsulfanylmethyl-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:57557-71-8 SDS

57557-71-8Relevant academic research and scientific papers

A Route to Organyl(trialkoxysilyl)chalcogenides and Dichalcogenides, Bis(trialkoxysilylmethyl)chalcogenides and Dichalcogenides

Sorokin, M. S.,Voronkov, M. G.

, p. 1883 - 1890 (2007/10/03)

Reactions of organylchalcogenomagnesium halides RYMgX (in situ) (R = Me, Et, Ph; Y = S, Se, Te; X = Br, I) with (halomethyl)trialkoxysilanes X'CH2Si(OR')3 (X' = Cl, I; R' = Me, Et) at reflux in tetra-hydrofuran and the systems of tetrahydrofuran-acetonitrile 1 :2, and ether-acetonitrile 1:2 are studied. These reactions are shown to lead to formation of mixtures of corresponding organyl(trialkoxysilylmethyl)chalcogenide and -dichalcogenide, bis(trialkoxysilyl methyl)chalcogenide and -dichalcogenide, as well as the contaminants 2,2,6,6-tetraalkoxy-2,6-disila-4-chalcogen-1-oxane, diorganylchalcogenide and -dichalcogenide, and other organic and organosilicon compounds. Composition of the formed mixtures depends considerably on the structure of R, nature of the chalcogen Y (S, Se, Te), and halides X and X' in the initial reagents, and reaction conditions. The most of synthesized and isolated organosilicon chalcogenides are newly obtained compounds.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 57557-71-8