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The chemical compound "2-({4-chloro-6-[4-(cyclopropylcarbonyl)piperazin-1-yl]pyrimidin-2-yl}sulfanyl)-N-[2-(2,4-dichlorophenyl)ethyl]acetamide" is a complex organic molecule with a molecular formula of C23H22Cl3N5O3S. It features a pyrimidinyl-sulfanyl group, a cyclopropylcarbonylpiperazinyl moiety, and a 2,4-dichlorophenylethylacetamide segment. 2-({4-chloro-6-[4-(cyclopropylcarbonyl)piperazin-1-yl]pyrimidin-2-yl}sulfanyl)-N-[2-(2,4-dichlorophenyl)ethyl]acetamide is characterized by the presence of multiple chlorine atoms, a cyclopropyl group, and a piperazine ring, which contribute to its unique chemical properties and potential applications in various fields, such as pharmaceuticals or chemical research. The specific arrangement of these functional groups and the overall structure of the molecule are crucial for understanding its reactivity and potential interactions with other substances.

5994-36-5

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5994-36-5 Usage

Molecular structure

2-(4-chloro-6-[4-(cyclopropylcarbonyl)piperazin-1-yl]pyrimidin-2-ylsulfanyl)-N-[2-(2,4-dichlorophenyl)ethyl]acetamide is a complex molecule consisting of a pyrimidine ring, a piperazine group, a chloro-substituted phenyl group, a thiol group, and an acetamide moiety.

Functional groups

The compound contains multiple functional groups, including a pyrrimidine ring, a piperazine group, a chloro-substituted phenyl group, a thiol group, and an acetamide moiety.

Potential pharmacological applications

The compound has potential effects on the central nervous system and may have anti-inflammatory properties.

Specific mechanism of action

The exact mechanism of action for 2-({4-chloro-6-[4-(cyclopropylcarbonyl)piperazin-1-yl]pyrimidin-2-yl}sulfanyl)-N-[2-(2,4-dichlorophenyl)ethyl]acetamide is not yet known and would require further experimental studies to determine its potential therapeutic uses.

Therapeutic uses

The potential therapeutic applications of 2-({4-chloro-6-[4-(cyclopropylcarbonyl)piperazin-1-yl]pyrimidin-2-yl}sulfanyl)-N-[2-(2,4-dichlorophenyl)ethyl]acetamide are not yet fully understood and would need to be investigated through additional research and experimentation.

Check Digit Verification of cas no

The CAS Registry Mumber 5994-36-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,9,9 and 4 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5994-36:
(6*5)+(5*9)+(4*9)+(3*4)+(2*3)+(1*6)=135
135 % 10 = 5
So 5994-36-5 is a valid CAS Registry Number.

5994-36-5SDS

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 2-ethyl-1-(2-oxo-2-phenylethyl)pyridin-1-ium bromide

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

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:5994-36-5 SDS

5994-36-5Relevant academic research and scientific papers

Indolizine-based chromophores with octatetraene π-bridge and tricyanofurane acceptor: Synthesis, photophysical, electrochemical and electro-optic properties

Kalinin, Alexey A.,Fazleeva, Guzel M.,Burganov, Timur I.,Islamova, Liliya N.,Dudkina, Yulia B.,Kadyrova, Alfira A.,Vakhonina, Tatyana A.,Khamatgalimov, Ayrat R.,Mukhtarov, Anvar S.,Bazarov, Valeriy V.,Katsyuba, Sergey A.,Budnikova, Yulia H.,Balakina, Marina Yu.

, (2019/10/11)

Two isomeric indolizine-based chromophores (MPI-1)-OT-TCF and (MPI-3)-OT-TCF with octatetraene π-bridge and tricyanofuran acceptor moieties have been synthesized and systematically investigated. Chromophores exist as a mixture of E- and Z-isomers in low-p

Synthesis and characterization of new second-order NLO chromophores containing the isomeric indolizine moiety for electro-optical materials

Kalinin, Alexey A.,Smirnov, Maxim A.,Islamova, Liliya N.,Fazleeva, Guzel M.,Vakhonina, Tatyana A.,Levitskaya, Alina I.,Fominykh, Olga D.,Ivanova, Nataliya V.,Khamatgalimov, Ayrat R.,Nizameev, Irek R.,Balakina, Marina Yu.

, p. 444 - 454 (2017/09/05)

To further explore the potential application of the indolizine donor group in nonlinear optical (NLO) chromophores, we have designed and synthesized new push-pull chromophores (MPI-1)-V-TCF and (MPI-3)-V-TCF, having isomeric 3(1)-methyl-2-phenylindolizin-

Application of DMF-methyl sulfate adduct in the regioselective synthesis of 3-acylated indolizines

Przewloka, Teresa,Chen, Shoujun,Xia, Zhiqiang,Li, Hao,Zhang, Shijie,Chimmanamada, Dinesh,Kostik, Elena,James, David,Koya, Keizo,Sun, Lijun

, p. 5739 - 5742 (2008/02/09)

A number of 3-acylated indolizines were synthesized in good to excellent yields by a newly established reaction between picolinium salts and the methylsulfate salt of A (R = Me), the adduct formed from DMF-Me2SO4 as the key reagent.

2-Phosphaindolizines

Bansal, Raj K.,Karaghiosoff, Konstantin,Gupta, Neelima,Schmidpeter, Alfred,Spindler, Claudia

, p. 475 - 480 (2007/10/02)

Pyridinium bromides 3 prepared by alkylation of 2-methyl-, 2-ethyl-, and 2-benzylpyridines 1 with methyl bromides 2 bearing an electron-withdrawing group (COPh, CN, CO2Et, C6H4NO2) are condensed with PCl3 in the presence of Et3N to give 2-phosphaindolizin

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