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6-Bromo-2-piperazin-1-yl-quinoline, a quinoline derivative with the molecular formula C14H14BrN3, is a chemical compound that features a piperazine moiety. This structure endows it with potential pharmacological properties, making it a candidate for medicinal applications. It has been the subject of research for its antimalarial and antitumor activities, and its unique structure also positions it as a valuable intermediate in the synthesis of pharmaceutical compounds. Furthermore, it holds promise for use in medicinal chemistry research and drug development.

124782-95-2

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124782-95-2 Usage

Uses

Used in Pharmaceutical Industry:
6-BROMO-2-PIPERAZIN-1-YL-QUINOLINE is used as a pharmacological agent for its potential antimalarial and antitumor properties, serving as a foundation for the development of new treatments in these therapeutic areas.
Used in Medicinal Chemistry Research:
6-BROMO-2-PIPERAZIN-1-YL-QUINOLINE is used as a research compound to explore its chemical and biological properties, contributing to the advancement of knowledge in medicinal chemistry.
Used in Drug Development:
6-BROMO-2-PIPERAZIN-1-YL-QUINOLINE is used as a synthetic intermediate in the creation of various pharmaceutical compounds, facilitating the design and synthesis of new drugs with potential therapeutic benefits.

Check Digit Verification of cas no

The CAS Registry Mumber 124782-95-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,7,8 and 2 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 124782-95:
(8*1)+(7*2)+(6*4)+(5*7)+(4*8)+(3*2)+(2*9)+(1*5)=142
142 % 10 = 2
So 124782-95-2 is a valid CAS Registry Number.
InChI:InChI=1/C13H14BrN3/c14-11-2-3-12-10(9-11)1-4-13(16-12)17-7-5-15-6-8-17/h1-4,9,15H,5-8H2

124782-95-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-bromo-2-piperazin-1-ylquinoline

1.2 Other means of identification

Product number -
Other names Quinoline,6-bromo-2-(1-piperazinyl)

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:124782-95-2 SDS

124782-95-2Downstream Products

124782-95-2Relevant academic research and scientific papers

BET INHIBITORS FOR MODULATING DUX4 EXPRESSION IN FSHD

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Page/Page column 296; 297, (2020/07/14)

The present disclosure provides BET inhibitors of the formula: wherein the variables are defined herein, as well as pharmaceutical compositions thereof. The present disclosure also provides methods of treating a patient comprising administering a bromo- and extra-terminal (BET) domain inhibitor for the treatment of FSHD which modulates DUX4 expression. In some embodiments, the present methods comprise using one or more BET inhibitors as a therapeutic agent for the treatment of FSHD patients including patients who are being treated with one or more palliative treatments such as therapy and/or agents which lead to increased muscle mass.

ANTIDEPRESSANT ARYLPIPERAZINE DERIVATIVES OF HETEROCYCLE-FUSED BENZODIOXANS

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Page 50-51, (2008/06/13)

Compounds of the formula I: are useful for the treatment of depression (including but not limited to major depressive disorder, childhood depression and dysthymia), anxiety, panic disorder, post-traumatic stress disorder, premenstrual dysphoric disorder (also known as pre-menstrual syndrome), attention deficit disorder (with and without hyperactivity), obsessive-compulsive disorder, social anxiety disorder, generalized anxiety disorder, obesity eating disorders such as anorexia nervosa and bulimia nervosa, vasomotor flushing, cocaine and alcohol addiction, sexual dysfunction and related illnesses.

Syntheses and binding affinities of 6-nitroquipazine analogues for serotonin transporter. Part 1

Lee, Byoung Se,Chu, Soyoung,Lee, Byung Chul,Chi, Dae Yoon,Choe, Yearn Seong,Jeong, Kyung Ja,Jin, Changbae

, p. 1559 - 1562 (2007/10/03)

6-Nitroquipazine has been known as one of the most potent and selective inhibitors of serotonin transporter in vitro and in vivo. Nine derivatives of 6-nitroquipazine were synthesized and tested for their potential abilities to displace [3H]citalopram binding to the rat cortical membranes. (C) 2000 Elsevier Science Ltd. All rights reserved.

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