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

160463-53-6

Post Buying Request

160463-53-6 Suppliers

Recommended suppliers

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

160463-53-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 160463-53-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,0,4,6 and 3 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 160463-53:
(8*1)+(7*6)+(6*0)+(5*4)+(4*6)+(3*3)+(2*5)+(1*3)=116
116 % 10 = 6
So 160463-53-6 is a valid CAS Registry Number.

160463-53-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-phenyl-1-triethylsilylethanone

1.2 Other means of identification

Product number -
Other names Silane,triethyl(phenylacetyl)

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:160463-53-6 SDS

160463-53-6Downstream Products

160463-53-6Relevant academic research and scientific papers

A synthesis of multisubstituted vinylsilanes via ynolates: Stereoselective formation of β-silyl-β-lactones followed by decarboxylation

Shindo, Mitsuru,Matsumoto, Kenji,Shishido, Kozo

, p. 2477 - 2479 (2007/10/03)

(Z)-Selective synthesis of multisubstituted vinylsilanes was achieved by stereoselective protonation or alkylation of β-silyl-β-lactone enolates, prepared by cycloadditions of acylsilanes with ynolates, followed by decarboxylation. The Royal Society of Ch

Conversion of Tellurol Esters to Enol Silyl Ethers of Acylsilanes

Inoue, Toru,Kambe, Nobuaki,Ryu, Ilhyong,Sonoda, Noboru

, p. 8209 - 8214 (2007/10/02)

Tellurol esters having an anion stabilizing group at the position α to the carbonyl, such as aryl-, (phenylthio)-, and (benzyloxy)ethanetelluroates, gave enol silyl ethers of the corresponding acylsilanes in good to excellent yields upon treatment with 2

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 160463-53-6