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"2-(carbamoylamino)-1-methyl-2-oxoethyl 2-(4-bromophenyl)quinoline-4-carboxylate" is a complex organic compound with the molecular formula C20H16BrN3O4. It is characterized by a quinoline-4-carboxylate core, which is substituted with a 4-bromophenyl group at the 2-position. The molecule also features a carbamoylamino group attached to a 1-methyl-2-oxoethyl moiety, which is connected to the quinoline core. 2-(carbamoylamino)-1-methyl-2-oxoethyl 2-(4-bromophenyl)quinoline-4-carboxylate is known for its potential applications in medicinal chemistry, particularly as a precursor in the synthesis of certain pharmaceuticals. Its structure and properties make it a subject of interest for researchers exploring new drug candidates and therapeutic agents.

5705-87-3

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5705-87-3 Usage

Carbamoylamino group

A functional group consisting of an amide and an amine group, which may contribute to the compound's biological activity as an enzyme inhibitor or receptor antagonist.

Methyl group

A small alkyl group with one carbon atom, which provides steric hindrance and may influence the compound's pharmacokinetic and pharmacodynamic properties.

Quinoline-4-carboxylate moiety

A heterocyclic aromatic ring system with a carboxylate group at the 4-position, which is known to be present in many pharmaceutical drugs and may contribute to the compound's pharmacological properties.

4-Bromophenyl substituent

A halogenated phenyl group attached to the quinoline ring, which may influence the compound's lipophilicity, stability, and biological activity.

Pharmacological properties

The presence of the quinoline ring suggests that 2-(carbamoylamino)-1-methyl-2-oxoethyl 2-(4-bromophenyl)quinoline-4-carboxylate may have potential pharmacological effects, possibly as an antimalarial, anti-inflammatory, or antimicrobial agent.

Biological activity

The carbamoylamino group indicates that the compound may have biological activity, potentially as an enzyme inhibitor or receptor antagonist, but further research is needed to confirm these properties.

Potential applications

Due to its complex structure and the presence of pharmacologically relevant functional groups, 2-(carbamoylamino)-1-methyl-2-oxoethyl 2-(4-bromophenyl)quinoline-4-carboxylate may have potential applications in the development of new drugs for various diseases and conditions. However, more research is required to fully understand its properties and potential uses.

Check Digit Verification of cas no

The CAS Registry Mumber 5705-87-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,7,0 and 5 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5705-87:
(6*5)+(5*7)+(4*0)+(3*5)+(2*8)+(1*7)=103
103 % 10 = 3
So 5705-87-3 is a valid CAS Registry Number.

5705-87-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name [1-(carbamoylamino)-1-oxopropan-2-yl] 2-(4-bromophenyl)quinoline-4-carboxylate

1.2 Other means of identification

Product number -
Other names -

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

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More Details:5705-87-3 SDS

5705-87-3Downstream Products

5705-87-3Relevant academic research and scientific papers

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