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2-Propen-1-one, 1-[2,4-bis(methoxymethoxy)phenyl]-3-[3,4-bis(methoxymethoxy)phenyl]- is a complex organic compound characterized by its unique molecular structure. It is a derivative of 2-propen-1-one, also known as acrolein, which is a basic building block in organic chemistry. The compound features two phenyl rings, each substituted with methoxymethoxy groups at the 2 and 4 positions. These substitutions significantly alter the chemical properties and reactivity of the molecule, making it a potentially valuable intermediate in the synthesis of various pharmaceuticals, agrochemicals, or other specialty chemicals. The specific arrangement and bonding of these functional groups contribute to the compound's stability and its potential applications in advanced material science.

6515-03-3

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6515-03-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6515-03-3 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, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6515-03:
(6*6)+(5*5)+(4*1)+(3*5)+(2*0)+(1*3)=83
83 % 10 = 3
So 6515-03-3 is a valid CAS Registry Number.

6515-03-3Downstream Products

6515-03-3Relevant 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 (2017/07/17)

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.

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