Cas 1253228-04-4,5,7,4'-triacetoxy-6-C-(2,3,4-tri-O-acetyl-β-D-xylopyranosyl)-8-C-(2,3,4-tri-O-acetyl-α-D-arabinopyranosyl)flavone

1253228-04-4

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Basic information

Product Name: 5,7,4'-triacetoxy-6-C-(2,3,4-tri-O-acetyl-β-D-xylopyranosyl)-8-C-(2,3,4-tri-O-acetyl-α-D-arabinopyranosyl)flavone
Synonyms: 5,7,4'-triacetoxy-6-C-(2,3,4-tri-O-acetyl-β-D-xylopyranosyl)-8-C-(2,3,4-tri-O-acetyl-α-D-arabinopyranosyl)flavone
CAS NO:1253228-04-4
Molecular Formula:
Molecular Weight: 912.809
EINECS: N/A
Product Categories: N/A
Mol File: 1253228-04-4.mol
Article Data: 1

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: 5,7,4'-triacetoxy-6-C-(2,3,4-tri-O-acetyl-β-D-xylopyranosyl)-8-C-(2,3,4-tri-O-acetyl-α-D-arabinopyranosyl)flavone(CAS DataBase Reference)
NIST Chemistry Reference: 5,7,4'-triacetoxy-6-C-(2,3,4-tri-O-acetyl-β-D-xylopyranosyl)-8-C-(2,3,4-tri-O-acetyl-α-D-arabinopyranosyl)flavone(1253228-04-4)
EPA Substance Registry System: 5,7,4'-triacetoxy-6-C-(2,3,4-tri-O-acetyl-β-D-xylopyranosyl)-8-C-(2,3,4-tri-O-acetyl-α-D-arabinopyranosyl)flavone(1253228-04-4)

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: 1253228-04-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1253228-04-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,5,3,2,2 and 8 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1253228-04:
(9*1)+(8*2)+(7*5)+(6*3)+(5*2)+(4*2)+(3*8)+(2*0)+(1*4)=124
124 % 10 = 4
So 1253228-04-4 is a valid CAS Registry Number.

1253228-04-4Upstream product

108-24-7 acetic anhydride

1253228-04-4Downstream Products

1253228-10-2 6-C-β-D-xylopyranosyl-8-C-α-D-arabinopyranosyl-5,7,4'-trihydroxyflavone

1253228-04-4Relevant articles and documents

Regioselective synthesis of di-C-glycosylflavones possessing anti-inflammation activities

Shie, Jiun-Jie,Chen, Chih-An,Lin, Chih-Chien,Ku, Angela Fay,Cheng, Ting-Jen R.,Fang, Jim-Min,Wong, Chi-Huey

, p. 4451 - 4462 (2010)

Three methods are utilized to synthesize a variety of 6,8-di-C- glycosylflavones bearing identical or distinct glycosyl moieties. Some C-glycosylation compounds are found to have better anti-inflammation activities than the parent flavones. Among them, 6,8-di-C-glucosylapigenin (known as vicenin-2) shows inhibition of TNF-α expression and NO production with IC50 values of 6.8 and 5.2 μM, respectively.

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