Cas 690274-21-6,4H-1-Benzopyran-4-one, 7-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-2,3-dihydro-3-(1-methylethyl)-2-[ 4-[2-(1-piperidinyl)ethoxy]phenyl]-

690274-21-6

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Basic information

Product Name: 4H-1-Benzopyran-4-one, 7-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-2,3-dihydro-3-(1-methylethyl)-2-[ 4-[2-(1-piperidinyl)ethoxy]phenyl]-
Synonyms:
CAS NO:690274-21-6
Molecular Formula: C31H45NO4Si
Molecular Weight: 523.788
EINECS: N/A
Product Categories: N/A
Mol File: 690274-21-6.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: 4H-1-Benzopyran-4-one, 7-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-2,3-dihydro-3-(1-methylethyl)-2-[ 4-[2-(1-piperidinyl)ethoxy]phenyl]-(CAS DataBase Reference)
NIST Chemistry Reference: 4H-1-Benzopyran-4-one, 7-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-2,3-dihydro-3-(1-methylethyl)-2-[ 4-[2-(1-piperidinyl)ethoxy]phenyl]-(690274-21-6)
EPA Substance Registry System: 4H-1-Benzopyran-4-one, 7-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-2,3-dihydro-3-(1-methylethyl)-2-[ 4-[2-(1-piperidinyl)ethoxy]phenyl]-(690274-21-6)

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: 690274-21-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 690274-21-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,9,0,2,7 and 4 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 690274-21:
(8*6)+(7*9)+(6*0)+(5*2)+(4*7)+(3*4)+(2*2)+(1*1)=166
166 % 10 = 6
So 690274-21-6 is a valid CAS Registry Number.

690274-21-6Upstream product

690274-21-6Downstream Products

690274-21-6Relevant articles and documents

Estrogen receptor ligands. Part 1: The discovery of flavanoids with subtype selectivity

Chen, Helen Y.,Dykstra, Kevin D.,Birzin, Elizabeth T.,Frisch, Katalin,Chan, Wanda,Yang, Yi T.,Mosley, Ralph T.,DiNinno, Frank,Rohrer, Susan P.,Schaeffer, James M.,Hammond, Milton L.

, p. 1417 - 1421 (2007/10/03)

A class of flavanoids exhibiting a high degree of selectivity for ERα over ERβ has been discovered. The most active analogue 6 was found to be 66-fold ERα-selective and demonstrated uterine estradiol antagonism.

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