Welcome to LookChem.com Sign In|Join Free
  • or
Ethanone,1,1'-(2,3,5,6-tetramethyl-1,4-phenylene)bis- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

15517-58-5

Post Buying Request

15517-58-5 Suppliers

Recommended suppliers

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

15517-58-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 15517-58-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,5,1 and 7 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 15517-58:
(7*1)+(6*5)+(5*5)+(4*1)+(3*7)+(2*5)+(1*8)=105
105 % 10 = 5
So 15517-58-5 is a valid CAS Registry Number.

15517-58-5SDS

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 1-(4-acetyl-2,3,5,6-tetramethylphenyl)ethanone

1.2 Other means of identification

Product number -
Other names 1,4-Diacetoxypentan

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:15517-58-5 SDS

15517-58-5Relevant academic research and scientific papers

Transition metal free α-C-alkylation of ketones using secondary alcohols

Dambatta, Mubarak B.,Santos, Joseph,Bolt, Robert R.A.,Morrill, Louis C.

supporting information, (2020/09/18)

A base-mediated α-C-alkylation of ketones with secondary alcohols has been developed. This transition metal free approach employs KOt-Bu as the base and exhibits a broad scope, allowing a range of commodity aliphatic secondary alcohols and 1-arylethanols

Hydrogen Borrowing Catalysis with Secondary Alcohols: A New Route for the Generation of β-Branched Carbonyl Compounds

Akhtar, Wasim M.,Cheong, Choon Boon,Frost, James R.,Christensen, Kirsten E.,Stevenson, Neil G.,Donohoe, Timothy J.

supporting information, p. 2577 - 2580 (2017/03/01)

A hydrogen borrowing reaction employing secondary alcohols and Ph? (Me5C6) ketones to give β-branched carbonyl products is described (21 examples). This new C-C bond forming process requires low loadings of [Cp?IrCl2]2, relatively low temperatures, and up to 2.0 equiv of the secondary alcohol. Substrate-induced diastereoselectivity was observed, and this represents the first example of a diastereoselective enolate hydrogen borrowing alkylation. By utilizing the Ph? group, the β-branched products could be straightforwardly cleaved to the corresponding esters or amides using a retro-Friedel-Crafts reaction. Finally, this protocol was applied to the synthesis of fragrance compound (±)-3-methyl-5-phenylpentanol.

NOVEL INITIATORS FOR LIVING CARBOCATIONIC POLYMERIZATION

-

Paragraph 0092; 0093, (2017/09/05)

In various embodiments, the present invention is directed to new low cost initiator compositions for use with the production of well-defined telechelic PIBs (by LC+P of isobutylene). In various other embodiments, the present invention is directed to metho

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 15517-58-5