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4,4'-diacetoxy-3,3'-dimethoxystilbene is a synthetic organic compound characterized by its unique molecular structure. It is a stilbene derivative, which means it has a core structure consisting of two phenyl rings connected by a double bond. This particular compound is distinguished by the presence of acetoxy groups at the 4 and 4' positions, and methoxy groups at the 3 and 3' positions. These functional groups contribute to its chemical properties and potential applications. The acetoxy groups are ester derivatives of acetic acid, while the methoxy groups are ether derivatives of methanol. 4,4'-diacetoxy-3,3'-dimethoxystilbene may be of interest in chemical research, particularly in the fields of organic synthesis and materials science, due to its specific functional groups and the potential for further chemical modifications.

7329-59-1

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7329-59-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7329-59-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,3,2 and 9 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 7329-59:
(6*7)+(5*3)+(4*2)+(3*9)+(2*5)+(1*9)=111
111 % 10 = 1
So 7329-59-1 is a valid CAS Registry Number.

7329-59-1Relevant academic research and scientific papers

Flash-metathesis for the coupling of sustainable (poly)hydroxyl β-methylstyrenes from essential oils

Hitce,Crutizat,Bourdon,Vivès,Marat,Dalko-Csiba

supporting information, p. 3756 - 3761 (2015/07/15)

A cross-metathesis procedure was developed to synthetize symmetrical and non symmetrical stilbenes from sustainable resources. The reaction proceeds under solvent-free conditions and at low catalyst loading (down to 0.01 mol%) within a couple of minutes only (TOF up to 6.9 s-1), on multi-gram scale. The highly reactive β-methylstyrene substrates were homo-coupled not only as pure synthons but also as components of essential oils that were reacted directly in order to eliminate prior substrate isolation from the overall process.

Cytoprotective compounds, pharmaceutical and cosmetic formulations, and methods

-

, (2008/06/13)

Cytoprotective compounds, many of which are phenolic derivatives characterized by a substituted phenol having certain conjugated bonds, are useful in the treatment of certain ischemic or inflammatory conditions, including but not limited to stroke, myocardial infarction, congestive heart failure, and skin disorders characterized by inflammation or oxidative damage. They are also useful in the manufacture of pharmaceutical and cosmetic formulations for the treatment of such conditions.

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