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Ethyl 2-(3,4,5-trimethoxybenzoyl)heptanoate is a complex organic compound with the chemical formula C18H28O6. It is a derivative of heptanoic acid, featuring a 3,4,5-trimethoxybenzoyl group attached to the second carbon of the heptanoate chain. ethyl 2-(3,4,5-trimethoxybenzoyl)heptanoate is characterized by its ester functional group, which is formed by the reaction of the carboxylic acid group of heptanoic acid with ethanol. The presence of three methoxy groups on the benzene ring of the trimethoxybenzoyl moiety contributes to its unique chemical properties. Ethyl 2-(3,4,5-trimethoxybenzoyl)heptanoate is often used in the synthesis of various pharmaceuticals and fragrances due to its specific scent and reactivity. Its molecular structure and functional groups make it a versatile building block in organic chemistry, particularly in the creation of complex molecules with potential applications in the chemical and pharmaceutical industries.

1574-99-8

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1574-99-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1574-99-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,7 and 4 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1574-99:
(6*1)+(5*5)+(4*7)+(3*4)+(2*9)+(1*9)=98
98 % 10 = 8
So 1574-99-8 is a valid CAS Registry Number.

1574-99-8Downstream Products

1574-99-8Relevant academic research and scientific papers

Synthesis of Dithiolethiones and Identification of Potential Neuroprotective Agents via Activation of Nrf2-Driven Antioxidant Enzymes

Bai, Feifei,Fang, Jianguo,Song, Zi-Long,Zhang, Baoxin

, p. 2214 - 2231 (2020/03/06)

Oxidative stress is implicated in the pathogenesis of a wide variety of neurodegenerative disorders, and accordingly, dietary supplement of exogenous antioxidants or/and upregulation of the endogenous antioxidant defense system are promising for therapeutic intervention or chemoprevention of neurodegenerative diseases. Nrf2, a master regulator of the cellular antioxidant machinery, cardinally participates in the transcription of cytoprotective genes against oxidative/electrophilic stresses. Herein, we report the synthesis of 59 structurally diverse dithiolethiones and evaluation of their neuroprotection against 6-hydroxydopamine-or H2O2-induced oxidative damages in PC12 cells, a neuron-like rat pheochromocytoma cell line. Initial screening identified compounds 10 and 11 having low cytotoxicity but conferring remarkable protection on PC12 cells from oxidative-mediated damages. Further studies demonstrated that both compounds upregulated a battery of antioxidant genes as well as corresponding genes' products. Significantly, silence of Nrf2 expression abolishes cytoprotection of 10 and 11, indicating targeting Nrf2 activation is pivotal for their cellular functions. Taken together, the two lead compounds discovered here with potent neuroprotective functions against oxidative stress via Nrf2 activation merit further development as therapeutic or chemopreventive candidates for neurodegenerative disorders.

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