Cas 130548-63-9,(6aR,9aS,11aR)-4-methyl-9-<2-(3'-O-tosyl-1',2'-O-isopropylidene-α-D-xylopentafuranoso)acetoxymethyl>-1,2,6a,7,10,10a-hexahydrothieno<3,2-a>anthracene-3,3,6,11-tetraone

130548-63-9

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Product Name: (6aR,9aS,11aR)-4-methyl-9-<2-(3'-O-tosyl-1',2'-O-isopropylidene-α-D-xylopentafuranoso)acetoxymethyl>-1,2,6a,7,10,10a-hexahydrothieno<3,2-a>anthracene-3,3,6,11-tetraone
Synonyms:
CAS NO:130548-63-9
Molecular Formula:
Molecular Weight: 700.785
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: (6aR,9aS,11aR)-4-methyl-9-<2-(3'-O-tosyl-1',2'-O-isopropylidene-α-D-xylopentafuranoso)acetoxymethyl>-1,2,6a,7,10,10a-hexahydrothieno<3,2-a>anthracene-3,3,6,11-tetraone(CAS DataBase Reference)
NIST Chemistry Reference: (6aR,9aS,11aR)-4-methyl-9-<2-(3'-O-tosyl-1',2'-O-isopropylidene-α-D-xylopentafuranoso)acetoxymethyl>-1,2,6a,7,10,10a-hexahydrothieno<3,2-a>anthracene-3,3,6,11-tetraone(130548-63-9)
EPA Substance Registry System: (6aR,9aS,11aR)-4-methyl-9-<2-(3'-O-tosyl-1',2'-O-isopropylidene-α-D-xylopentafuranoso)acetoxymethyl>-1,2,6a,7,10,10a-hexahydrothieno<3,2-a>anthracene-3,3,6,11-tetraone(130548-63-9)

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: 130548-63-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 130548-63-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,5,4 and 8 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 130548-63:
(8*1)+(7*3)+(6*0)+(5*5)+(4*4)+(3*8)+(2*6)+(1*3)=109
109 % 10 = 9
So 130548-63-9 is a valid CAS Registry Number.

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130548-63-9Relevant academic research and scientific papers

Cycloaddition of glycosylated butadienes in the synthesis of natural quinone analogs

Vafina,Spirikhin,Shul'ts,Tolstikov

, p. 386 - 395 (2007/10/03)

Diels-Alder reactions of naphthoquinones with substituted hydroxybutadienes containing a carbohydrate moiety proceed in a regioselective fashion, yielding the corresponding C-glycosylated anthraquinones. A nucleoside having an anthraquinone fragment was s

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