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2-(4-ETHYLPIPERAZIN-1-YL)BENZALDEHYDE is a chemical compound with the formula C14H18N2O. It is a benzaldehyde derivative with a piperazine group attached to the 2-position, making it a potential ligand for various receptors and enzymes. 2-(4-ETHYLPIPERAZIN-1-YL)BENZALDEHYDE has been studied for its potential pharmacological applications, including its effects on the central nervous system. Additionally, it has been investigated for its potential use in medicinal chemistry and drug design. The 4-ethylpiperazine group in the molecule may contribute to its interactions with biological targets, and further research is ongoing to explore its potential uses in various fields.

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  • 865203-79-8 Structure
  • Basic information

    1. Product Name: 2-(4-ETHYLPIPERAZIN-1-YL)BENZALDEHYDE
    2. Synonyms: 2-(4-ETHYLPIPERAZIN-1-YL)BENZALDEHYDE
    3. CAS NO:865203-79-8
    4. Molecular Formula: C13H18N2O
    5. Molecular Weight: 218.29
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 865203-79-8.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 346.4°C at 760 mmHg
    3. Flash Point: 146.4°C
    4. Appearance: /
    5. Density: 1.08g/cm3
    6. Vapor Pressure: 5.78E-05mmHg at 25°C
    7. Refractive Index: 1.568
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 2-(4-ETHYLPIPERAZIN-1-YL)BENZALDEHYDE(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2-(4-ETHYLPIPERAZIN-1-YL)BENZALDEHYDE(865203-79-8)
    12. EPA Substance Registry System: 2-(4-ETHYLPIPERAZIN-1-YL)BENZALDEHYDE(865203-79-8)
  • Safety Data

    1. Hazard Codes: Xi
    2. Statements: 36
    3. Safety Statements: 26
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 865203-79-8(Hazardous Substances Data)

865203-79-8 Usage

Uses

Used in Pharmaceutical Industry:
2-(4-ETHYLPIPERAZIN-1-YL)BENZALDEHYDE is used as a potential ligand for various receptors and enzymes due to its unique chemical structure and the presence of the 4-ethylpiperazine group, which may contribute to its interactions with biological targets.
Used in Medicinal Chemistry and Drug Design:
2-(4-ETHYLPIPERAZIN-1-YL)BENZALDEHYDE is used as a compound of interest in the development of new drugs and therapeutic agents, given its potential pharmacological applications and its effects on the central nervous system.
Used in Research and Development:
2-(4-ETHYLPIPERAZIN-1-YL)BENZALDEHYDE is used as a subject of ongoing research to explore its potential uses in various fields, including its interactions with biological targets and its potential applications in the treatment of various conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 865203-79-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,5,2,0 and 3 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 865203-79:
(8*8)+(7*6)+(6*5)+(5*2)+(4*0)+(3*3)+(2*7)+(1*9)=178
178 % 10 = 8
So 865203-79-8 is a valid CAS Registry Number.
InChI:InChI=1/C13H18N2O/c1-2-14-7-9-15(10-8-14)13-6-4-3-5-12(13)11-16/h3-6,11H,2,7-10H2,1H3

865203-79-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-ETHYLPIPERAZIN-1-YL)BENZALDEHYDE

1.2 Other means of identification

Product number -
Other names 2-(2-METHOXY-4-(TRIFLUOROMETHYL)PHENYL)-4,4,6-TRIMETHYL-1,3,2-DIOXABORINANE

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:865203-79-8 SDS

865203-79-8Downstream Products

865203-79-8Relevant articles and documents

Ruthenium catalyzed β-C(sp3)-H functionalization on the 'privileged' piperazine nucleus

Murugesh,Bruneau, Christian,Achard, Mathieu,Sahoo, Apurba Ranjan,Sharma, Gangavaram V. M.,Suresh, Surisetti

supporting information, p. 10448 - 10451 (2017/09/25)

β-C(sp3)-H functionalization on the 'privileged' piperazine nucleus has been disclosed using ruthenium catalysis. The ruthenium catalyzed synthesis of a variety of piperazine fused indoles from ortho-piperazinyl (hetero)aryl aldehydes is presented. This transformation takes place via the dehydrogenation of piperazine followed by an intramolecular nucleophilic addition of the transient enamine moiety onto the carbonyl group and aromatization cascade.

Design, synthesis and anticancer activity of functionalized spiro-quinolines with barbituric and thiobarbituric acids

Bhaskarachar, Ravi Kiran,Revanasiddappa, Vijayakumar G.,Hegde, Subramanya,Balakrishna, Janardhana P.,Reddy, Suman Y.

, p. 3516 - 3528 (2015/08/03)

A new series of spiro-quinoline compounds have been accomplished by the reaction of barbituric acid or thiobarbituric acid with derivatives of benzisoxazole-5-carbaldehyde or 2-substituted benzaldehyde. These compounds were evaluated for their in vitro cy

NOVEL BENZYL(IDENE)-LACTAM DERIVATIVES

-

Page/Page column 32, (2008/06/13)

The present invention relates to novel benzyl(idene)-lactam derivatives, compounds of the formula (I) wherein R1 is a group of the formula G1 or G2 depicted below, wherein R1, R3, R6, R13, X, a, n and m are as defined herein, their pharmaceutically acceptable salts, and pharmaceutical compositions which include selective antagonists, inverse agonists and partial agonists of serotonin 1 (5-HT1) receptors, specifically, of one or both of the 5-HT1A and 5-HT1B receptors. The compounds of the invention are useful in treating or preventing depression, anxiety, obsessive compulsive disorder (OCD) and other disorders for which a 5-HT1 agonist or antagonist is indicated and have reduced potential for cardiac side effects, in particular QTc prolongation.

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