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1-(4-BroMophenyl)-3-pyrrolidinol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

536742-64-0

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536742-64-0 Usage

Uses

1-(4-Bromophenyl)-3-pyrrolidinol used in antitumor studies.

Check Digit Verification of cas no

The CAS Registry Mumber 536742-64-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,3,6,7,4 and 2 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 536742-64:
(8*5)+(7*3)+(6*6)+(5*7)+(4*4)+(3*2)+(2*6)+(1*4)=170
170 % 10 = 0
So 536742-64-0 is a valid CAS Registry Number.

536742-64-0SDS

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 1-(4-bromo-phenyl)-pyrrolidin-3-ol

1.2 Other means of identification

Product number -
Other names 1-(4-Bromophenyl)-3-pyrrolidinol

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:536742-64-0 SDS

536742-64-0Relevant academic research and scientific papers

Ruthenium catalyzed amination cyclization of 1,2,4-butanetriol with primary amines: A borrowing hydrogen strategy for 3-pyrrolidinol synthesis

Xu, Qing-Song,Li, Chen,Xu, Yong,Xu, Defeng,Shen, Mei-Hua,Xu, Hua-Dong

supporting information, (2019/06/04)

A ruthenium based catalytic system ([Ru(p-cymene)Cl2]2/XantPhos with substoichiometric Cs2CO3) has been established to effectively achieve the first direct amination cyclization of 1,2,4-butanetriol with primary

COMPOUNDS AND COMPOSITIONS AS MODULATORS OF GPR119 ACTIVITY

-

Page/Page column 139, (2008/12/08)

The invention provides compounds, pharmaceutical compositions comprising such compounds and methods of using such compounds to treat or prevent diseases or disorders associated with the activity of GPR119.

Alkyne compounds with MCH antagonistic activity and medicaments comprising these compounds

-

Page/Page column 31, (2010/02/14)

Alkyne compounds of formula I wherein A, B, W, X, Y, Z, R1, and R2 have the meanings given herein, which have MCH-receptor antagonistic activity and are useful for preparing pharmaceutical compositions for the treatment of metabolic disorders and/or eating disorders, particularly obesity and diabetes.

NOVEL ALKYNE COMPOUNDS HAVING AN MCH-ANTAGONISTIC EFFECT, AND MEDICAMENTS CONTAINING SAID COMPOUNDS

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Page/Page column 82; 83, (2010/02/14)

The invention relates to alkyne compounds of general formula (I), wherein the groups and radicals A, B, W, X, Y, Z, R1, and R2 have the meanings indicated in claim 1. The invention further relates to medicaments containing at least one inventive alkyne. The disclosed medicaments are suitable for the treatment of metabolic disorders and/or eating disorders, particularly adiposity and diabetes, as a result of the MCH receptor antagonistic activity thereof.

Non-classical antifolates, 5-(N-phenylpyrrolidin-3-yl)-2,4,6-triaminopyrimidines and 2,4-Diamino-6(5H)-oxopyrimidines, synthesis and antitumor studies

Huang, Yen-Lin,Lin, Chyun-Feng,Lee, Yi-Jen,Li, Wei-Wei,Chao, Ting-Chou,Bacherikov, Valeriy A.,Chen, Kuo-Tung,Chen, Chin-Ming,Su, Tsann-Long

, p. 145 - 157 (2007/10/03)

A series of non-classical antifolates, namely 5-(N-phenylpyrrolidin-3-yl)-2,4,6-triaminopyrimidines (25a-i) and 2,4-diamino-(N-phenylpyrrolidin-3-yl)-6(5H)-oxopyrimidines (26a,b,c,f,h,i) was synthesized and evaluated for their in vitro cytotoxicity. React

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