Welcome to LookChem.com Sign In|Join Free
  • or
9,10-Anthracenedione, 1,3,8-trimethoxy-6-methyl- is a chemical compound with the molecular formula C17H16O5. It is a derivative of anthraquinone, a type of organic compound that consists of two benzene rings fused together with a carbonyl group in the center. This specific compound features three methoxy groups (-OCH3) attached to the 1, 3, and 8 positions of the anthraquinone structure, as well as a methyl group (-CH3) at the 6 position. The compound is known for its potential applications in the synthesis of various dyes and pharmaceuticals, and it is characterized by its unique chemical structure and properties.

6414-42-2

Post Buying Request

6414-42-2 Suppliers

Recommended suppliers

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

6414-42-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6414-42-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,4,1 and 4 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6414-42:
(6*6)+(5*4)+(4*1)+(3*4)+(2*4)+(1*2)=82
82 % 10 = 2
So 6414-42-2 is a valid CAS Registry Number.

6414-42-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3,8-trimethoxy-6-methylanthracene-9,10-dione

1.2 Other means of identification

Product number -
Other names 1,3,8-Trimethoxy-6-methyl-anthraquinone

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:6414-42-2 SDS

6414-42-2Relevant academic research and scientific papers

REACTIONS OF KETENE ACETALS-14; THE USE OF SIMPLE MIXED VINYLKETENE ACETALS IN THE ANNULATION OF QUINONES

Savard, Jacques,Brassard, Paul

, p. 3455 - 3464 (1984)

α,β- and β,γ-unsaturated esters can be converted by strong base and chlorotrimethylsilane to the corresponding mixed vinylketene acetals which are shown to be particularly useful and generally applicable reagents for the regiospecific annulation of halogenoquinones.The reaction proceeds readily with a variety of substrates including benzoquinones.

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 6414-42-2