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Benzenesulfonamide, 4-[6-methoxy-1-[4-[2-(1-piperidinyl)ethoxy]phenoxy]-2-naphthalenyl]-N,N-dimethyl- is a complex organic compound with the chemical formula C28H30N2O4S. It is a derivative of benzenesulfonamide, featuring a naphthalene ring with various substituents, including a methoxy group, a piperidinyl-ethoxy group, and a dimethylamino group. Benzenesulfonamide, 4-[6-methoxy-1-[4-[2-(1-piperidinyl)ethoxy]phenoxy]-2-naphthalenyl]-N,N -dimethyl- is known for its potential applications in pharmaceuticals, particularly as a serotonin receptor agonist, and is used in the synthesis of drugs targeting central nervous system disorders. Its structure and properties make it a significant molecule in the field of medicinal chemistry.

648905-66-2

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648905-66-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 648905-66-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,4,8,9,0 and 5 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 648905-66:
(8*6)+(7*4)+(6*8)+(5*9)+(4*0)+(3*5)+(2*6)+(1*6)=202
202 % 10 = 2
So 648905-66-2 is a valid CAS Registry Number.

648905-66-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-{6-methoxy-1-[4-(2-piperidin-1-yl-ethoxy)-phenoxy]-naphthalen-2-yl}-N,N-dimethylbenzenesulfonamide

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

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More Details:648905-66-2 SDS

648905-66-2Relevant academic research and scientific papers

Structure-activity relationships of SERMs optimized for uterine antagonism and ovarian safety

Richardson, Timothy I.,Frank, Scott A.,Wang, Minmin,Clarke, Christian A.,Jones, Scott A.,Ying, Bai-Ping,Kohlman, Dan T.,Wallace, Owen B.,Shepherd, Timothy A.,Dally, Robert D.,Palkowitz, Alan D.,Geiser, Andrew G.,Bryant, Henry U.,Henck, Judith W.,Cohen, Ilene R.,Rudmann, Daniel G.,McCann, Denis J.,Coutant, David E.,Oldham, Samuel W.,Hummel, Conrad W.,Fong, Kin C.,Hinklin, Ronald,Lewis, George,Tian, Hongqi,Dodge, Jeffrey A.

, p. 3544 - 3549 (2008/02/07)

Structure-activity relationship studies are described, which led to the discovery of novel selective estrogen receptor modulators (SERMs) for the potential treatment of uterine fibroids. The SAR studies focused on limiting brain exposure and were guided by computational properties. Compounds with limited impact on the HPO axis were selected using serum estrogen levels as a biomarker for ovarian stimulation.

SELECTIVE ESTROGEN RECEPTOR MODULATORS CONTAINING A PHENYLSULFONYL GROUP

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Page/Page column 61, (2008/06/13)

The present invention relates to a selective estrogen receptor modulator of formula I or a pharmaceutical acid addition salt thereof; useful, e.g., for treating endometriosis and/or uterine leiomyoma/leiomyomata.

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