Welcome to LookChem.com Sign In|Join Free
  • or
1,2-Diacetoxy-9,10-anthraquinone is a chemical compound with the molecular formula C16H12O6. It is a derivative of anthraquinone, a type of organic compound that is widely used in the dye industry. This specific compound features two acetoxy groups attached to the 1 and 2 positions of the anthraquinone core, which gives it unique properties and potential applications. It is often used as an intermediate in the synthesis of various dyes and pigments, particularly those with anthraquinone-based structures. The compound is known for its stability and can be synthesized through various chemical reactions, making it a valuable component in the production of a range of colorants for textiles, plastics, and other materials.

1629-51-2

Post Buying Request

1629-51-2 Suppliers

Recommended suppliers

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

1629-51-2 Usage

Derivative of

Anthraquinone

Common uses

a. Redox catalyst
b. Intermediate in the production of dyes and pigments

Potential applications

a. Organic synthesis
b. Production of advanced materials

Stability

Stable

Versatility

Can undergo various reactions to form a wide range of products

Unique chemical properties

Valuable component in the production of industrial and consumer products

Check Digit Verification of cas no

The CAS Registry Mumber 1629-51-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,2 and 9 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1629-51:
(6*1)+(5*6)+(4*2)+(3*9)+(2*5)+(1*1)=82
82 % 10 = 2
So 1629-51-2 is a valid CAS Registry Number.

1629-51-2Relevant academic research and scientific papers

Different synthetic routes towards efficient organogelators: 2,3-substituted anthracenes

Pozzo, Jean-Luc,Clavier, Gilles M.,Colomes, Michel,Bouas-Laurent, Henri

, p. 6377 - 6390 (2007/10/03)

Three synthetic approaches towards 2,3-substituted anthracenes are reported and discussed in terms of selectivity and viability. This allowed us to introduce a variety of substituents as sidearms. Promising results have been found using a tandem Diels-Alder aromatization reaction using 2,2,3-dimethoxybuladiene 9 as a key intermediate. However, for multigram preparations the Friedel-Crafts approach is preferred.

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 1629-51-2