Welcome to LookChem.com Sign In|Join Free
  • or
2',4'-Bis-methoxymethoxy-chalkon, also known as 2',4'-bis-(methoxymethoxy)-1,4-naphthoquinone, is a synthetic organic compound characterized by the presence of two methoxymethoxy groups attached to the 2' and 4' positions of a naphthoquinone backbone. This molecule is of interest in chemical research due to its potential applications in various fields, including the synthesis of pharmaceuticals and dyes. The methoxymethoxy groups contribute to the compound's reactivity and solubility properties, making it a valuable intermediate in the preparation of more complex molecules. The structure of 2',4'-bis-methoxymethoxy-chalkon allows for further functionalization and modification, which can lead to the development of new compounds with specific therapeutic or industrial applications.

6515-12-4

Post Buying Request

6515-12-4 Suppliers

Recommended suppliers

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

6515-12-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6515-12-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,5,1 and 5 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6515-12:
(6*6)+(5*5)+(4*1)+(3*5)+(2*1)+(1*2)=84
84 % 10 = 4
So 6515-12-4 is a valid CAS Registry Number.

6515-12-4Downstream Products

6515-12-4Relevant academic research and scientific papers

Design, synthesis and bioactivity of chalcones and its analogues

Niu, Chao,Tuerxuntayi, Adila,Li, Gen,Kabas, Madina,Dong, Chang-Zhi,Aisa, Haji Akber

, p. 1533 - 1538 (2017)

The Vernohia anthelmintica L.'s extract is one of the most popular Uygur medicines used for vitiligo. It is believed that the chalcone compounds of the plant play an important role in the treatment since they may activate tyrosinase and improve melanin production. In this study, twenty-one chalcones and nine analogues were synthesized in view of three different components of chalcone (A, B ring and α, β-unsaturated carbonyl). After biological evaluation of their activity on tyrosinase in cell-free systems, the result showed that most compounds (except polyhydroxy chalcones) possess activator effect on the tyrosinase, especially for 13a–15a, 20a and 1b, which bearing a comparable activity to the positive control 8-MOP. SAR of these tyrosinase activator was summed up for the first time as well. Finally, compound 13a was found to increase melanin contents and tyrosinase activity 1.75 and 1.3 fold, respectively, compared with that of untreated murine B16 cells at the concentration of 40?μg/mL.

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 6515-12-4