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[1,4'-Bipiperidine]-1'-carboxylic acid, 4-[(4-bromophenyl)methyl]-, 1,1-dimethylethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

203187-19-3

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203187-19-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 203187-19-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,3,1,8 and 7 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 203187-19:
(8*2)+(7*0)+(6*3)+(5*1)+(4*8)+(3*7)+(2*1)+(1*9)=103
103 % 10 = 3
So 203187-19-3 is a valid CAS Registry Number.

203187-19-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Methyl-2-propanyl 4-(4-bromobenzyl)-1,4'-bipiperidine-1'-carbox ylate

1.2 Other means of identification

Product number -
Other names 4-(4-bromo-benzyl)-[1,4']bipiperidinyl-1'-carboxylic acid tert-butyl ester

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

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:203187-19-3 SDS

203187-19-3Relevant academic research and scientific papers

MUSCARINIC M2 RECEPTOR BLOCKADE TO DELAY OR PREVENT ONSET OF PROGRESSIVE MEMORY DECLINE

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Paragraph 0016; 0056, (2018/10/04)

Provided are methods for delaying or preventing onset of progressive memory decline by administering a muscarinic M2 receptor blocking compound to patients identified as at risk of developing a condition characterized by progressive memory decline, prior

The synthesis of substituted bipiperidine amide compounds as CCR3 antagonists

Ting, Pauline C.,Lee, Joe F.,Wu, Jie,Umland, Shelby P.,Aslanian, Robert,Cao, Jianhua,Dong, Youhao,Garlisi, Charles G.,Gilbert, Eric J.,Huang, Ying,Jakway, James,Kelly, Joseph,Liu, Zhidan,McCombie, Stuart,Shah, Himanshu,Tian, Fang,Wan, Yuntao,Shih, Neng-Yang

, p. 1375 - 1378 (2007/10/03)

Bipiperidine amide 1 has been identified as a CC chemokine receptor 3 (CCR3) antagonist. Optimization of its structure-activity relationship has resulted in the identification of cis (R,R)-4-[(3,4-dichlorophenyl)methyl]-3- hydroxymethyl-1′(6-quinolinylcar

Isopropyl amide derivatives of potent and selective muscarinic M 2 receptor antagonists

Palani, Anandan,Dugar, Sundeep,Clader, John W.,Greenlee, William J.,Ruperto, Vilma,Duffy, Ruth A.,Lachowicz, Jean E.

, p. 1791 - 1794 (2007/10/03)

Low molecular weight amide derivatives were synthesized and evaluated as M2 receptor antagonists for the treatment of Alzheimer's disease. Isopropyl amides 19 and 31 are highly potent, selective and low molecular weight M2 receptor a

Muscarinic M2 antagonists: Anthranilamide derivatives with exceptional selectivity and in vivo activity

Clader, John W.,Billard, William,Binch III, Herbert,Chen, Lian-Yong,Crosby Jr., Gordon,Duffy, Ruth A.,Ford, Jennifer,Kozlowski, Joseph A.,Lachowicz, Jean E.,Li, Shengjian,Liu, Charles,McCombie, Stuart W.,Vice, Susan,Zhou, Gowei,Greenlee, William J.

, p. 319 - 326 (2007/10/03)

Anthranilamide analogues such as 23 are potent and highly selective muscarinic M2 antagonists that also show good oral bioavailability and in vivo activity.

MUSCARINIC ANTAGONISTS

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Page 23, (2010/02/06)

Amide derivatives of 1,4 di-substituted piperidine compounds of formula (I) or a pharmaceutically acceptable salt, ester or solvate thereof, wherein Q and Q are each -CH=, or one of Q and Q is -CH= and the other is -N=; X is -CH2- or (a); Y and Z are -C(R)=, or one of Y and Z is -C(R)= and the other is -N=; R is 1 to 3 substituents selected from H, halogen and alkoxy; R and R are 1 to 3 substituents selected from H, halogen, alkyl and alkoxy; and R and R are H or (C1-C6) alkyl are muscarinic antagonists usuful for treating cognitive disorders such as Alzheimer's disease. Pharmaceutical compositions and methods of preparation are also disclosed.

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