Cas 1104455-75-5,acetic acid 9-[3,17β-bisbenzyloxyestra-1,3,5(10)-trien-11β-yl]-3,3,4,4,5,5,6,6-octafluorononyl ester

1104455-75-5

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Basic information

Product Name: acetic acid 9-[3,17β-bisbenzyloxyestra-1,3,5(10)-trien-11β-yl]-3,3,4,4,5,5,6,6-octafluorononyl ester
Synonyms: acetic acid 9-[3,17β-bisbenzyloxyestra-1,3,5(10)-trien-11β-yl]-3,3,4,4,5,5,6,6-octafluorononyl ester
CAS NO:1104455-75-5
Molecular Formula:
Molecular Weight: 780.839
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: acetic acid 9-[3,17β-bisbenzyloxyestra-1,3,5(10)-trien-11β-yl]-3,3,4,4,5,5,6,6-octafluorononyl ester(CAS DataBase Reference)
NIST Chemistry Reference: acetic acid 9-[3,17β-bisbenzyloxyestra-1,3,5(10)-trien-11β-yl]-3,3,4,4,5,5,6,6-octafluorononyl ester(1104455-75-5)
EPA Substance Registry System: acetic acid 9-[3,17β-bisbenzyloxyestra-1,3,5(10)-trien-11β-yl]-3,3,4,4,5,5,6,6-octafluorononyl ester(1104455-75-5)

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: 1104455-75-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1104455-75-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,0,4,4,5 and 5 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1104455-75:
(9*1)+(8*1)+(7*0)+(6*4)+(5*4)+(4*5)+(3*5)+(2*7)+(1*5)=115
115 % 10 = 5
So 1104455-75-5 is a valid CAS Registry Number.

1104455-75-5Upstream product

1104455-75-5Downstream Products

1104455-88-0 9-(3,17β-bisbenzyloxyestra-1,3,5(10)-trien-11β-yl)-3,3,4,4,5,5,6,6-octafluorononan-1-ol

1104455-75-5Relevant academic research and scientific papers

Effect of fluorination on the pharmacological profile of 11β isomers of fulvestrant in breast carcinoma cells

Agouridas, Vangelis,Magnier, Emmanuel,Blazejewski, Jean-Claude,La?os, Ioanna,Cleeren, Anny,Nonclercq, Denis,Laurent, Guy,Leclercq, Guy

experimental part, p. 883 - 887 (2009/11/30)

We describe the synthesis of an 11/β isomer 3 of the steroidal antiestrogen fulvestrant 2. Partial fluorination of the 11β side chain in 3 leads to 4, which still shows strong antiproliferative activity on MCF-7 cells. However, unlike 2 and 3, compound 4

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