Cas 1599463-45-2,diosgenyl 2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl-(1→2)-[2,3,4-tri-O-benzoyl-α-D-lyxopyranosyl-(1→3)]-4,6-di-O-benzylidene-β-D-galactopyranoside

1599463-45-2

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Product Name: diosgenyl 2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl-(1→2)-[2,3,4-tri-O-benzoyl-α-D-lyxopyranosyl-(1→3)]-4,6-di-O-benzylidene-β-D-galactopyranoside
Synonyms: diosgenyl 2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl-(1→2)-[2,3,4-tri-O-benzoyl-α-D-lyxopyranosyl-(1→3)]-4,6-di-O-benzylidene-β-D-galactopyranoside
CAS NO:1599463-45-2
Molecular Formula:
Molecular Weight: 1381.58
EINECS: N/A
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Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: diosgenyl 2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl-(1→2)-[2,3,4-tri-O-benzoyl-α-D-lyxopyranosyl-(1→3)]-4,6-di-O-benzylidene-β-D-galactopyranoside(CAS DataBase Reference)
NIST Chemistry Reference: diosgenyl 2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl-(1→2)-[2,3,4-tri-O-benzoyl-α-D-lyxopyranosyl-(1→3)]-4,6-di-O-benzylidene-β-D-galactopyranoside(1599463-45-2)
EPA Substance Registry System: diosgenyl 2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl-(1→2)-[2,3,4-tri-O-benzoyl-α-D-lyxopyranosyl-(1→3)]-4,6-di-O-benzylidene-β-D-galactopyranoside(1599463-45-2)

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RTECS:
HazardClass: N/A
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Hazardous Substances Data: 1599463-45-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1599463-45-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,9,9,4,6 and 3 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1599463-45:
(9*1)+(8*5)+(7*9)+(6*9)+(5*4)+(4*6)+(3*3)+(2*4)+(1*5)=232
232 % 10 = 2
So 1599463-45-2 is a valid CAS Registry Number.

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1599463-45-2Relevant academic research and scientific papers

Efficient synthesis and antitumor activities of indioside e analogs

Zhao, Yisheng,An, Lian,Gu, Guofeng,Guo, Zhongwu

, p. 152 - 168 (2014/05/06)

An efficient synthesis of seven analogs of a naturally occurring saponin, indioside E, is described. The synthesis used a 3,4,6-O-protected D-galactopyranosyl thioglycoside as the key intermediate to enable regioselective glycosylation and one-pot multistep reactions. Antitumor activities of the synthetic saponins against a human hepatocellular carcinoma cell line BEL-7402 and a human breast adenocarcinoma cell line MCF-7 were evaluated by means of the CCK-8 assay. Analogs carrying trisaccharides with the D-xylopyranose in indioside E substituted with a D-ribopyranose and an L-arabinopyranose or with its diosgenin aglycon replaced with tigogenin exhibited similar antitumor activities as indioside E, but not other analogs.

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