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324750-04-1

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324750-04-1 Usage

General Description

N4-Benzyl-2-ethylpiperazine is a chemical compound with the molecular formula C14H24N2. It is a piperazine derivative that is commonly used in the synthesis of pharmaceuticals and organic compounds. N4-BENZYL-2-ETHYLPIPERAZINE is known for its diverse range of biological activities, including its role as a potential dopamine receptor antagonist and its ability to bind with serotonin receptors. N4-Benzyl-2-ethylpiperazine has also been studied for its potential use in the treatment of psychiatric disorders and neurological conditions. Additionally, it has been investigated for its potential as an anticancer agent. Overall, N4-Benzyl-2-ethylpiperazine is a versatile compound with potential applications in various fields of research and medicine.

Check Digit Verification of cas no

The CAS Registry Mumber 324750-04-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,4,7,5 and 0 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 324750-04:
(8*3)+(7*2)+(6*4)+(5*7)+(4*5)+(3*0)+(2*0)+(1*4)=121
121 % 10 = 1
So 324750-04-1 is a valid CAS Registry Number.
InChI:InChI=1/C13H20N2/c1-2-13-11-15(9-8-14-13)10-12-6-4-3-5-7-12/h3-7,13-14H,2,8-11H2,1H3/t13-/m0/s1

324750-04-1 Well-known Company Product Price

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  • Alfa Aesar

  • (H52557)  (S)-1-Benzyl-3-ethylpiperazine, 97%   

  • 324750-04-1

  • 250mg

  • 1764.0CNY

  • Detail
  • Alfa Aesar

  • (H52557)  (S)-1-Benzyl-3-ethylpiperazine, 97%   

  • 324750-04-1

  • 1g

  • 5292.0CNY

  • Detail

324750-04-1SDS

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 (3S)-1-benzyl-3-ethylpiperazine

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:324750-04-1 SDS

324750-04-1Relevant articles and documents

Catalytic Asymmetric Synthesis of Morpholines. Using Mechanistic Insights to Realize the Enantioselective Synthesis of Piperazines

Lau, Ying Yin,Zhai, Huimin,Schafer, Laurel L.

, p. 8696 - 8709 (2016/10/14)

An efficient and practical catalytic approach for the enantioselective synthesis of 3-substituted morpholines through a tandem sequential one-pot reaction employing both hydroamination and asymmetric transfer hydrogenation reactions is described. Starting from ether-containing aminoalkyne substrates, a commercially available bis(amidate)bis(amido)Ti catalyst is utilized to yield a cyclic imine that is subsequently reduced using the Noyori-Ikariya catalyst, RuCl [(S,S)-Ts-DPEN] (η6-p-cymene), to afford chiral 3-substituted morpholines in good yield and enantiomeric excesses of >95%. A wide range of functional groups is tolerated. Substrate scope investigations suggest that hydrogen-bonding interactions between the oxygen in the backbone of the ether-containing substrate and the [(S,S)-Ts-DPEN] ligand of the Ru catalyst are crucial for obtaining high ee's. This insight led to a mechanistic proposal that predicts the observed absolute stereochemistry. Most importantly, this mechanistic insight allowed for the extension of this strategy to include N as an alternative hydrogen bond acceptor that could be incorporated into the substrate. Thus, the catalytic, enantioselective synthesis of 3-substituted piperazines is also demonstrated.

Novel Compounds

-

Page/Page column 20, (2008/12/04)

The invention relates to substituted aryl acids as useful pharmaceutical compounds for treating respiratory disorders, pharmaceutical compositions containing them, and processes for their preparation.

PIPERAZINE UREA DERIVATIVES AS MELANOCORTIN-4 RECEPTOR AGONISTS

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Page 80, (2010/11/30)

Certain novel piperazine urea derivatives are agonists of the human melanocortin-4 receptor (MC-4R) and, in particular, are receptor-subtype selective agonists of MC-4R. They are useful for the treatment, control, or prevention of diseases and disorders r

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