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94110-86-8

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94110-86-8 Usage

Description

Ethyl 8-nitro-4-oxo-3,4-dihydroquinoline-3-carboxylate is a complex chemical compound belonging to the quinoline class, characterized by the presence of a nitro group, a carbonyl group, and an ethyl ester functional group. It may hold potential in medicinal chemistry due to the pharmacological properties often associated with quinoline derivatives, such as anti-inflammatory and antimicrobial activities.

Uses

Used in Medicinal Chemistry:
Ethyl 8-nitro-4-oxo-3,4-dihydroquinoline-3-carboxylate is used as a potential pharmaceutical agent for its possible anti-inflammatory and antimicrobial properties, leveraging the known pharmacological activities of quinoline derivatives.
Further research and testing are required to determine the specific applications and efficacy of ethyl 8-nitro-4-oxo-3,4-dihydroquinoline-3-carboxylate in various fields, including but not limited to drug development for treating inflammation and infections.

Check Digit Verification of cas no

The CAS Registry Mumber 94110-86-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,1,1 and 0 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 94110-86:
(7*9)+(6*4)+(5*1)+(4*1)+(3*0)+(2*8)+(1*6)=118
118 % 10 = 8
So 94110-86-8 is a valid CAS Registry Number.

94110-86-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name Ethyl 8-nitro-4-oxo-3,4-dihydro-3-quinolinecarboxylate

1.2 Other means of identification

Product number -
Other names 8-nitro-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid ethyl 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:94110-86-8 SDS

94110-86-8Relevant articles and documents

Investigations on the 4-quinolone-3-carboxylic acid motif. 4. Identification of new potent and selective ligands for the cannabinoid type 2 receptor with diverse substitution patterns and antihyperalgesic effects in mice

Pasquini, Serena,De Rosa, Maria,Pedani, Valentina,Mugnaini, Claudia,Guida, Francesca,Luongo, Livio,De Chiaro, Maria,Maione, Sabatino,Dragoni, Stefania,Frosini, Maria,Ligresti, Alessia,Di Marzo, Vincenzo,Corelli, Federico

supporting information; experimental part, p. 5444 - 5453 (2011/09/30)

Experimental evidence suggests that selective CB2 receptor modulators may provide access to antihyperalgesic agents devoid of psychotropic effects. Taking advantage of previous findings on structure-activity/selectivity relationships for a class of 4-quin

QUINOLINE DERIVATIVES AS CASPASE-3 INHIBITOR, PREPARATION FOR PRODUCING THE SAME AND PHARMACEUTICAL COMPOSITION COMPRISING THE SAME

-

Page/Page column 27-28, (2008/06/13)

The present invention relates to new quinoline derivatives of formula (1) or their pharmaceutically acceptable salts with caspase-3 inhibitory activity and their preparation methods, wherein R2 is H; halogen; C1-6alkyl; C 1-6 alkoxy; C1-6 alkoxyalkyl; or C3-6cycloalkyl; R1 is formula (a); -CN; or formula (b); R is H; C6-14aryl unsubstituted or substituted by halogen, C1-6 alkyl, C1-6 alkoxy or amino; 5 - 15 membered heterocyclic group unsubstituted or substituted by halogen, C1-6 alkyl, C1-6 alkoxy or amino; or -(CH2)n-CHR4R5. The present invention relates to a pharmaceutical composition for treating caspase-associated diseases by inhibiting the activity of caspase-3 which comprises the compound of formula (1) or its pharmaceutically acceptable salt.

Synthesis and antiallergic activity of some quinolinones and imidazoquinolinones

Peet,Baugh,Sunder,Lewis

, p. 298 - 302 (2007/10/02)

A group of 1,4-dihydro-4-oxoquinoline-2- and 3-carboxylic acid esters with nitrogen functionality at the 8-position was synthesized, and 6-oxo-6H-imidazo[4,5,1-ij]quinoline-4- and 5-carboxylic acid esters were elaborated from these. Several of the compoun

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