Welcome to LookChem.com Sign In|Join Free
  • or
1-Propanone, 3-(4-methyl-1,4-etheno-2,3-benzodioxin-1(4H)-yl)-1-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

109986-19-8

Post Buying Request

109986-19-8 Suppliers

Recommended suppliers

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

109986-19-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 109986-19-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,9,9,8 and 6 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 109986-19:
(8*1)+(7*0)+(6*9)+(5*9)+(4*8)+(3*6)+(2*1)+(1*9)=168
168 % 10 = 8
So 109986-19-8 is a valid CAS Registry Number.

109986-19-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(1,4-epidioxy-1,4-dihydro-4-methylnaphth-1-yl)-1-phenylpropanone

1.2 Other means of identification

Product number -
Other names 3-(8-Methyl-9,10-dioxa-tricyclo[6.2.2.02,7]dodeca-2(7),3,5,11-tetraen-1-yl)-1-phenyl-propan-1-one

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:109986-19-8 SDS

109986-19-8Downstream Products

109986-19-8Relevant academic research and scientific papers

The Formation of Bridged Bicyclic 1,2,4-Trioxanes by Intramolecular Capture of β-Hydroperoxy Cations

Jefford, Charles W.,Favarger, France,Ferro, Serenella,Chambaz, Daniel,Bringhen, Alain,et al.

, p. 1778 - 1786 (2007/10/02)

The 1,4-endoperoxide, prepared from 3-(4-methylnaphth-1-yl) propanal by photo-oxygenation in CH2Cl2, gave on treatment with Amberlyst-15, 3,10b-epidioxy-2,3,4a,10b-tetrahydro-6-methyl-1H-naphthopyran in 85percent yield.Its structure was determined by X-ray crystal structure analysis.The 1,2,4-trioxane moiety is locked in a twist-boat conformation with trans fusion to the parent six-membered ring.The 1,4-endoperoxides of the methyl, butyl, and phenyl ketone analogues of the aforementioned aldehyde underwent similar acid-catalyzed rearrangement to the corresponding bridged bicyclic trioxanes in 94,47, and 48percent yelds, respectively.

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 109986-19-8