Welcome to LookChem.com Sign In|Join Free
  • or
2,5-Bis-(3,4-dimethoxy-phenyl)-furan is a complex organic compound characterized by a furan ring structure, which is a five-membered aromatic ring containing one oxygen atom. The compound is distinguished by two 3,4-dimethoxy-phenyl groups attached to the 2 and 5 positions of the furan ring. Each of these phenyl groups has two methoxy substituents at the 3 and 4 positions, which are electron-donating groups that can influence the compound's reactivity and physical properties. This specific arrangement of functional groups endows the molecule with unique chemical and electronic properties, making it a subject of interest in various fields, including materials science and medicinal chemistry.

4650-69-5

Post Buying Request

4650-69-5 Suppliers

Recommended suppliers

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

4650-69-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4650-69-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,6,5 and 0 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 4650-69:
(6*4)+(5*6)+(4*5)+(3*0)+(2*6)+(1*9)=95
95 % 10 = 5
So 4650-69-5 is a valid CAS Registry Number.

4650-69-5Relevant academic research and scientific papers

Synthesis and?evaluation of?cytotoxic activity of?arylfurans

de Oliveira, Renata B.,de Souza-Fagundes, Elaine M.,Siqueira, Helen A.J.,Leite, Rodrigo S.,Donnici, Claudio L.,Zani, Carlos L.

, p. 756 - 760 (2007/10/03)

A series of 2-aryl and 2,5-diarylfurans were synthesized and evaluated for their in vitro cytotoxicity against human cancer cells lines and on the proliferation of human peripheral blood mononuclear cells (PBMC) stimulated with phytohemaglutinin (PHA). Three compounds were found to present significant activity against the cancer cell lines without affecting the lymphocyte proliferation in PBMCs, indicating low toxicity to normal cells.

Substituted furans as inhibitors of the PDE4 enzyme

Perrier, Helene,Bayly, Christopher,Laliberte, France,Huang, Zheng,Rasori, Roberta,Robichaud, Annette,Girard, Yves,Macdonald, Dwight

, p. 323 - 326 (2007/10/03)

The synthesis and in vitro activity of a series of substituted furans as a novel structural class of PDE4 inhibitors is described. Comparison of emetic threshold with known PDE4 inhibitors is presented.

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 4650-69-5