17345-66-3 Usage
Uses
Used in Dye and Pigment Production:
2,3,4-Trihydroxydiphenylmethane is used as a key intermediate in the production of dyes and pigments for various applications, including textiles, plastics, and printing inks. Its unique chemical structure contributes to the color intensity and stability of the resulting dyes and pigments.
Used in Pharmaceutical Applications:
Leveraging its antioxidant properties, 2,3,4-Trihydroxydiphenylmethane is employed in pharmaceutical formulations to combat oxidative stress and related conditions. Its presence in medications can help protect cells from damage caused by reactive oxygen species, contributing to the overall health and well-being of patients.
Used in Cosmetic Applications:
In the cosmetics industry, 2,3,4-Trihydroxydiphenylmethane is used as an antioxidant to protect skin from environmental stressors and to maintain the integrity of cosmetic products. Its inclusion in skincare and beauty products can help prevent premature aging and promote a healthy skin appearance.
Used in Chemical Reactions:
Due to its high reactivity, 2,3,4-Trihydroxydiphenylmethane serves as a versatile building block in various chemical reactions, enabling the synthesis of a wide range of compounds for different industries, such as pharmaceuticals, agrochemicals, and materials science. Its ability to participate in multiple types of chemical transformations makes it a valuable asset in the development of new and innovative products.
Check Digit Verification of cas no
The CAS Registry Mumber 17345-66-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,3,4 and 5 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 17345-66:
(7*1)+(6*7)+(5*3)+(4*4)+(3*5)+(2*6)+(1*6)=113
113 % 10 = 3
So 17345-66-3 is a valid CAS Registry Number.
InChI:InChI=1/C9H11F3O4/c1-3-16-8(15)6(4-5(2)13)7(14)9(10,11)12/h6H,3-4H2,1-2H3
17345-66-3Relevant academic research and scientific papers
New convenient approach for the synthesis of benzyl 2H-chromenones and their α-amylase inhibitory, ABTS+ scavenging activities
Kumar, Jaladi Ashok,Tiwari, Ashok Kumar,Saidachary, Gannerla,Kumar, Domati Anand,Ali, Zehra,Sridhar, Balasubramanian,Raju, Bhimapaka China
, p. 806 - 811 (2013/09/23)
Series of new benzyl 2H-chromenones 6a-n was synthesized by Pechmann condensation of substituted benzyl resorcinols 2a-c and 3a with various β-ketoesters such as ethyl 3-oxobutanoate, ethyl 3-oxo-3-phenylpropanoate, ethyl 4-chloro-3-oxobutanoate, ethyl 4,4,4-trifluoro-3-oxobutanoate and ethyl 2-chloro-3-oxobutanoate 5a-e in very good yields. Synthesized compounds 6a-n were screened for their α-amylase inhibitory, and ABTS+ scavenging activities. In the present series of compounds, compound 8-benzyl-7-hydroxy-4-phenyl-2H-chromen-2-one 6c and 8-benzyl-7-hydroxy-4-methyl- 2H-chromen-2-one 6a were most potent ABTS+ radical scavenging and α-amylase inhibitor. Although compound 6,8-dibenzyl-7-hydroxy-4- (trifluoromethyl)-2H-chromen-2-one 6h displayed potent ABTS+ free radical scavenging potential, it was found poor in inhibiting pancreatic α-amylase.
