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Retroresinolide is a naturally occurring chemical compound belonging to the class of diterpenes, which are derived from the resin of plants. It is characterized by its unique structure, featuring a retro-configuration, which means that the double bond in the molecule is arranged in a specific orientation that is different from the more common顺式 (cis) configuration. Retroresinolide has been found to exhibit various biological activities, such as anti-inflammatory and cytotoxic properties, making it a subject of interest in the field of natural product chemistry and pharmacology. The study of retroresinolide and its derivatives could potentially lead to the development of new therapeutic agents for treating various diseases.

3571-40-2

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3571-40-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3571-40-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,7 and 1 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 3571-40:
(6*3)+(5*5)+(4*7)+(3*1)+(2*4)+(1*0)=82
82 % 10 = 2
So 3571-40-2 is a valid CAS Registry Number.

3571-40-2Relevant academic research and scientific papers

SYNTHESIS OF DIARYLBUTANES FROM CORDIGERINES AND REINVESTIGATION OF THEIR OXIDATIVE COUPLINGS IN DEOXYSCHIZANDRINS. - AN UNUSUAL FORMATION OF PHENYLTETRALIN LIGNANS -

Landais, Y.,Lebrun, A.,Lenain, V.,Robin, J.-P.

, p. 5161 - 5164 (2007/10/02)

Dibenzylbutanolide lignans including cordigerines were synthetized and transformed in the corresponding diarylbutane lignans which were submitted to non-phenolic oxidative coupling conditions by using RuO2 or Tl2O3 in trifluoroacetic medium to give deoxyschizandrins.A concurently aryl-benzyl coupling leads to the formation of the corresponding phenyltetralin of which the structure was confirmed by total synthesis.

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