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103914-52-9

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103914-52-9 Usage

General Description

2-(4-Bromo-phenyl)-quinoline-4-carboxylic acid is a chemical compound with the molecular formula C16H10BrNO2. It is a quinoline derivative with a carboxylic acid group and a bromine-substituted phenyl ring. 2-(4-Bromo-phenyl)-quinoline-4-carboxylic acid has potential applications in pharmaceutical research and development due to its structural features and potential biological activities. It may also serve as a starting material or intermediate in the synthesis of other organic compounds. Overall, 2-(4-Bromo-phenyl)-quinoline-4-carboxylic acid is a versatile chemical with potential utility in various scientific and industrial fields.

Check Digit Verification of cas no

The CAS Registry Mumber 103914-52-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,9,1 and 4 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 103914-52:
(8*1)+(7*0)+(6*3)+(5*9)+(4*1)+(3*4)+(2*5)+(1*2)=99
99 % 10 = 9
So 103914-52-9 is a valid CAS Registry Number.
InChI:InChI=1/C16H10BrNO2/c17-11-7-5-10(6-8-11)15-9-13(16(19)20)12-3-1-2-4-14(12)18-15/h1-9H,(H,19,20)/p-1

103914-52-9SDS

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-(4-Bromophenyl)quinoline-4-carboxylic acid

1.2 Other means of identification

Product number -
Other names 2-(4-bromophenyl)quinoline-4-carboxylic acid

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:103914-52-9 SDS

103914-52-9Relevant articles and documents

Synthesis and Luminescent Properties of Eu3+, Gd3+, and Tb3+ Complexes with Quinoline-4-carboxylic Acids

Aksenov, N. A.,Aksenova, I. V.,Dotsenko, V. V.,Kolokolov, F. A.,Kotlova, I. A.

, p. 2413 - 2419 (2019)

New complex compounds LnL3·nH2O (n = 5–10) have been synthesized on the basis of Eu3+, Gd3+, and Tb3+ salts and quinoline-4-carboxylic acid derivatives obtained via the Pfitzinger reaction. Compositio

A highly selective and sensitive boronic acid-based sensor for detecting Pd2+ ion under mild conditions

Bian, Zhancun,Fang, Guiqian,Wang, Ran,Wu, Zhongyu,Yao, Qingqiang,Zhan, Dongxue,Zhang, Guimin

, (2020)

Herein, a boronic acid-based sensor was reported selectively to recognize Pd2+ ion. The fluorescence intensity increased 36-fold after sensor binding with 2.47 × 10?5 M of Pd2+ ion. It was carried out in the 99% aqueous so

Synthesis of Novel Quinoline–Benzoxazolinone Ester Hybrids: In Vitro Anti-Inflammatory Activity and Antibacterial Activity

Shaikh, Sarfaraz F.,Dhavan, Pratik P.,Singh, Pinky R.,Vaidya,Jadhav,Ramana

, p. 572 - 583 (2021/05/03)

Abstract: A series of novel quinoline-benzoxazolinone ester hybrids were synthesized characterized and assessed for their in vitro anti-inflammatory and antibacterial activity. The in vitro anti-inflammatory activity was executed using protein denaturation assay, proteinase inhibitory assay and human red blood cell membrane stabilization assay. Most of the compounds exhibited potential anti-inflammatory activity. Compound (2-oxobenzo[d]oxazol-3(2H)-yl)methyl-2-(thiophen-2-yl)quinoline-4-carboxylate showed a better anti-inflammatory activity than the standard drugs diclofenac sodium and indomethacin. Furthermore, antibacterial activities of the synthesized compounds were evaluated using resazurin microtiter assay (REMA) and were compared with a positive drug standard chloramphenicol. The compounds demonstrated moderate to potent antibacterial activity. (2-Oxobenzo[d]oxazol-3(2H)-yl)methyl-2-(3,4-dimethoxyphenyl)quinoline-4-carboxylate and (2-oxobenzo[d]oxazol-3(2H)-yl)methyl-2-(2-chlorophenyl)quinoline-4-carboxylate displayed excellent activity against all bacterial strains in comparison to standard chloramphenicol. Moreover, cytotoxicity was performed on MDCK cells using MTT assay and it was found that none of the synthesized derivatives possessed any cytotoxicity.

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