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5994-36-5

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  • 2-[4-chloro-6-[4-(cyclopropanecarbonyl)piperazin-1-yl]pyrimidin-2-yl]sulfanyl-N-[2-(2,4-dichlorophenyl)ethyl]acetamide

    Cas No: 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 this compound is not yet known and would require further experimental studies to determine its potential therapeutic uses.

Therapeutic uses

The potential therapeutic applications of this compound 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 articles and documents

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

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.

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