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methyl 2-(3,5-dimethoxy-1-methyloxycarbonyl-2,5-cyclohexadienyl)acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

358742-91-3

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358742-91-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 358742-91-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,8,7,4 and 2 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 358742-91:
(8*3)+(7*5)+(6*8)+(5*7)+(4*4)+(3*2)+(2*9)+(1*1)=183
183 % 10 = 3
So 358742-91-3 is a valid CAS Registry Number.

358742-91-3Relevant academic research and scientific papers

Synthesis and evaluation of 4-hydroxyphenylacetic acid amides and 4-hydroxycinnamamides as antioxidants

Jung, Young-Sik,Kang, Tae-Souk,Yoon, Joong-Ho,Joe, Bo-Young,Lim, Hee-Jong,Seong, Churl-Min,Park, Woo-Kyu,Kong, Jae-Yang,Cho, Jungsook,Park, No-Sang

, p. 2599 - 2602 (2007/10/03)

4-Hydroxyphenylacetic acid amides and 4-hydroxycinnamamides were synthesized and their antioxidant and neuroprotective activities were evaluated. Among the prepared compounds, 6f, 6g, 8b, and 9 exhibited potent inhibition of lipid peroxidation in rat brain homogenates, and marked DPPH radical scavenging activities. Furthermore, 6f, 6g, and 9 exhibited neuroprotective action against the oxidative damage induced by the exposure of primary cultured rat cortical cells to H2O2, xanthine/xanthine oxidase, or Fe2+/ascorbic acid. Based on these results, we found that 6f was the most potent antioxidant among the compounds tested.

Synthesis of 3-alkoxy-4-hydroxyphenylacetic acids from methyl 3-alkoxybenzoates

Jung,Kang,Lee,Seong,Ham,Park

, p. 455 - 462 (2007/10/03)

3-Alkoxy-4-hydroxyphenylacetic acids 4 were obtained from 3-alkoxyl-substituted methyl benzoates 1 by reductive alkylation, followed by allylic oxidation and hydrolysis.

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