Cas 1227475-59-3,(1R,3S,3aR,8bS)-3a-(4-bromophenyl)-6,8-dimethoxy-3-phenyl-2,3,3a,8b-tetrahydro-1H-cyclopenta[b]benzofuran-1,8b-diol

1227475-59-3

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Basic information

Product Name: (1R,3S,3aR,8bS)-3a-(4-bromophenyl)-6,8-dimethoxy-3-phenyl-2,3,3a,8b-tetrahydro-1H-cyclopenta[b]benzofuran-1,8b-diol
Synonyms:
CAS NO:1227475-59-3
Molecular Formula:
Molecular Weight: 483.359
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: (1R,3S,3aR,8bS)-3a-(4-bromophenyl)-6,8-dimethoxy-3-phenyl-2,3,3a,8b-tetrahydro-1H-cyclopenta[b]benzofuran-1,8b-diol(CAS DataBase Reference)
NIST Chemistry Reference: (1R,3S,3aR,8bS)-3a-(4-bromophenyl)-6,8-dimethoxy-3-phenyl-2,3,3a,8b-tetrahydro-1H-cyclopenta[b]benzofuran-1,8b-diol(1227475-59-3)
EPA Substance Registry System: (1R,3S,3aR,8bS)-3a-(4-bromophenyl)-6,8-dimethoxy-3-phenyl-2,3,3a,8b-tetrahydro-1H-cyclopenta[b]benzofuran-1,8b-diol(1227475-59-3)

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: 1227475-59-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1227475-59-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,2,7,4,7 and 5 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1227475-59:
(9*1)+(8*2)+(7*2)+(6*7)+(5*4)+(4*7)+(3*5)+(2*5)+(1*9)=163
163 % 10 = 3
So 1227475-59-3 is a valid CAS Registry Number.

1227475-59-3Upstream product

1227475-68-4 C₂₅H₂₁BrO₅

1227475-59-3Downstream Products

1227475-59-3Relevant academic research and scientific papers

Novel flavaglines displaying improved cytotoxicity

Thuaud, Frédéric,Ribeiro, Nigel,Gaiddon, Christian,Cresteil, Thierry,Désaubry, Laurent

scheme or table, p. 411 - 415 (2011/03/19)

Novel flavagline analogues were synthesized and examined with respect to their cytotoxicity. Structural features critical to the potential of this class of anticancer natural products were unraveled. We demonstrated, in particular, that the introduction o

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