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Lup-20(29)-ene-3β,28-diyl dibenzoate is a naturally occurring chemical compound derived from plants, specifically from the lupine family. It is a diterpene, a class of organic compounds that are derived from the isoprene unit. lup-20(29)-ene-3β,28-diyl dibenzoate is characterized by its unique molecular structure, which includes a dibenzoate group attached to a lup-20(29)-ene-3β,28-diyl moiety. The dibenzoate group is an ester formed from the reaction of a diol (in this case, the lup-20(29)-ene-3β,28-diyl) with benzoic acid. lup-20(29)-ene-3β,28-diyl dibenzoate is of interest in the field of natural products chemistry and may have potential applications in pharmaceuticals or as a chemical intermediate. However, further research is needed to fully understand its properties and potential uses.

5354-50-7

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5354-50-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5354-50-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,5 and 4 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5354-50:
(6*5)+(5*3)+(4*5)+(3*4)+(2*5)+(1*0)=87
87 % 10 = 7
So 5354-50-7 is a valid CAS Registry Number.

5354-50-7Downstream Products

5354-50-7Relevant academic research and scientific papers

Ferrocenyltriazoles from 3β,28-Diacylbetulin: Synthesis and Cytotoxic Activity

Glushkov,Shemyakina,Zhukova,Pavlogradskaya,Dmitriev,Eroshenko,Galeev,Mokrushin

, p. 1690 - 1697 (2019)

The reaction of 30-bromo-3β,28-diacylbetulin with sodium azide afforded 30-azido-3β,28-diacyloxylup-20(29)-enes. The products were subjected to a CuI/TMEDA-catalyzed click reaction with ethynylferrocene to obtain the corresponding ferrocene-betulin conjug

Synthesis of Betulin Dibenzoate and Diphthalate

Levdanskii,Levdanskii,Kuznetsov

, p. 310 - 311 (2017/07/05)

Betulin-3,28-dibenzoate and -3,28-diphthalate were synthesized for the first time by reacting betulin with melts of benzoic and phthalic acids at 190–200°C for 5 min.

Synthesis and in vitro antitumor evaluation of betulin acid ester derivatives as novel apoptosis inducers

Yang, Sheng-Jie,Liu, Ming-Chuan,Xiang, Hong-Mei,Zhao, Qi,Xue, Wei,Yang, Song

, p. 249 - 255 (2015/08/24)

Nineteen betulin derivatives modified at the C-3 and C-28 positions were synthesized and assessed for antitumor activities against the MGC-803, PC3, Bcap-37, A375, and MCF-7 human cancer cell lines in vitro by MTT assay. Some derivatives (compounds 3a-3d

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