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28-O-tert-butyldiphenylsilyl-3β-O-(2,3,4-tri-O-benzoyl-α-L-arabinopyranosyl)betulin is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1104398-61-9

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1104398-61-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1104398-61-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,0,4,3,9 and 8 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1104398-61:
(9*1)+(8*1)+(7*0)+(6*4)+(5*3)+(4*9)+(3*8)+(2*6)+(1*1)=129
129 % 10 = 9
So 1104398-61-9 is a valid CAS Registry Number.

1104398-61-9Relevant academic research and scientific papers

Influence of intramolecular hydrogen bonds on regioselectivity of glycosylation. Synthesis of lupane-type saponins bearing the OSW-1 saponin disaccharide unit and its isomers

Kuczynska, Kinga,Cmoch, Piotr,Rárová, Lucie,Okle??ková, Jana,Korda, Anna,Pakulski, Zbigniew,Strnad, Miroslav

supporting information, p. 49 - 69 (2016/02/20)

A series of lupane-type saponins bearing OSW-1 disaccharide unit as well as its regio- and stereoisomers were prepared and used for the structure-activity relationships (SAR) study. Unexpected preference for 1→4-linked regioisomers and an unusual inversio

BIDESMOSIDIC BETULIN AND BETULINIC ACID DERIVATIVES AND USES THEREOF AS ANTITUMOR AGENTS

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Page/Page column 33, (2010/04/06)

The instant application is directed to bidesmosidic betulin and betulinic acid saponin derivatives of formula (I), and use thereof as antitumor agents. In particular, said compounds are effective in treating lung carcinomas, colorectal adenocarcinomas, br

Synthesis and cytotoxicity of bidesmosidic betulin and betulinic acid saponins

Gauthier, Charles,Legault, Jean,Lavoie, Serge,Rondeau, Simon,Tremblay, Samuel,Pichette, Andre

experimental part, p. 72 - 81 (2009/05/26)

The naturally occurring cytotoxic saponin 28-O-β-D- glucopyranosylbetulinic acid 3β-O-α-L-arabinopyranoside (3) was easily synthesized along with seven bidesmosidic saponins starting from the lupane-type triterpenoids betulin (1) and betulinic acid (2). A

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