Cas 592550-52-2,[12β,20(S),25-trihydroxydammar-3-O-β-D-glucopyranosyl-(1→2)-β-D-glucopyranoside]

592550-52-2

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Basic information

Product Name: [12β,20(S),25-trihydroxydammar-3-O-β-D-glucopyranosyl-(1→2)-β-D-glucopyranoside]
Synonyms: [12β,20(S),25-trihydroxydammar-3-O-β-D-glucopyranosyl-(1→2)-β-D-glucopyranoside]
CAS NO:592550-52-2
Molecular Formula:
Molecular Weight: 803.041
EINECS: N/A
Product Categories: N/A

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: [12β,20(S),25-trihydroxydammar-3-O-β-D-glucopyranosyl-(1→2)-β-D-glucopyranoside](CAS DataBase Reference)
NIST Chemistry Reference: [12β,20(S),25-trihydroxydammar-3-O-β-D-glucopyranosyl-(1→2)-β-D-glucopyranoside](592550-52-2)
EPA Substance Registry System: [12β,20(S),25-trihydroxydammar-3-O-β-D-glucopyranosyl-(1→2)-β-D-glucopyranoside](592550-52-2)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 592550-52-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 592550-52-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,9,2,5,5 and 0 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 592550-52:
(8*5)+(7*9)+(6*2)+(5*5)+(4*5)+(3*0)+(2*5)+(1*2)=172
172 % 10 = 2
So 592550-52-2 is a valid CAS Registry Number.

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592550-52-2Relevant academic research and scientific papers

Conversion of ginsenoside RB1 into six types of highly bioactive ginsenoside Rg3 and its derivatives by FeCl3 catalysis

Yu, Hongshan,Wang, Yu,Liu, Chunying,Yang, Jiamei,Xu, Longquan,Li, Guanheng,Song, Jianguo,Jin, Fengxie

, p. 901 - 906 (2018)

Ginsenoside Rb1 is an important saponin of ginseng(s); however, Rb1, with 3-O- and 20-O-sugar moieties, has low bioavailability. Here, we report the derivatization of ginsenoside Rb1 to completely generate six types of highly bioactive minor ginsenoside R

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