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2-(4-Benzylpiperazino)benzaldehyde is an organic compound with a unique structure that combines benzaldehyde and piperazine components. It has the chemical formula C19H20N2O and a molecular weight of 292.37 g/mol. This aromatic aldehyde is characterized by a benzene ring with a formyl group attached, and the benzylpiperazine moiety, which is a six-membered ring containing two nitrogen atoms. 2-(4-BENZYLPIPERAZINO)BENZALDEHYDE is primarily utilized in scientific research and has potential applications in the pharmaceutical industry. Its properties and characteristics can be influenced by factors such as temperature, pressure, and concentration.

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  • 112253-26-6 Structure
  • Basic information

    1. Product Name: 2-(4-BENZYLPIPERAZINO)BENZALDEHYDE
    2. Synonyms: 2-(4-BENZYLPIPERAZINO)BENZALDEHYDE;2-(4-BENZYLPIPERAZINO)BENZENECARBALDEHYDE;2-(4-BENZYLPIPERAZIN-1-YL)BENZALDEHYDE;2-(4-BENZYLPIPERAZIN-1-YL)BENZALDEHYDE, 95+%;1-Benzyl-4-(2-formylphenyl)piperazine
    3. CAS NO:112253-26-6
    4. Molecular Formula: C18H20N2O
    5. Molecular Weight: 280.36
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 112253-26-6.mol
  • Chemical Properties

    1. Melting Point: 58 °C
    2. Boiling Point: 429.9 °C at 760 mmHg
    3. Flash Point: 184.1 °C
    4. Appearance: /
    5. Density: 1.155 g/cm3
    6. Vapor Pressure: 1.36E-07mmHg at 25°C
    7. Refractive Index: N/A
    8. Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
    9. Solubility: N/A
    10. PKA: 7.46±0.10(Predicted)
    11. CAS DataBase Reference: 2-(4-BENZYLPIPERAZINO)BENZALDEHYDE(CAS DataBase Reference)
    12. NIST Chemistry Reference: 2-(4-BENZYLPIPERAZINO)BENZALDEHYDE(112253-26-6)
    13. EPA Substance Registry System: 2-(4-BENZYLPIPERAZINO)BENZALDEHYDE(112253-26-6)
  • Safety Data

    1. Hazard Codes: Xi
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: IRRITANT
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 112253-26-6(Hazardous Substances Data)

112253-26-6 Usage

Uses

Used in Scientific Research:
2-(4-Benzylpiperazino)benzaldehyde is used as a research compound for studying its chemical properties and potential interactions with other molecules. Its unique structure allows for exploration in various fields of chemistry and material science.
Used in Pharmaceutical Development:
2-(4-Benzylpiperazino)benzaldehyde is used as a starting material or intermediate in the synthesis of pharmaceutical compounds. Its structural components, including the benzaldehyde and piperazine moieties, can be exploited to develop new drugs with potential therapeutic applications.
Used in Chemical Synthesis:
2-(4-Benzylpiperazino)benzaldehyde is used as a reagent in the synthesis of various organic compounds. Its aromatic aldehyde and piperazine components can be utilized to create a wide range of chemical products, including dyes, pigments, and other specialty chemicals.
Used in Material Science:
2-(4-Benzylpiperazino)benzaldehyde is used in the development of new materials with specific properties. Its structural features can be incorporated into the design of advanced materials, such as polymers, coatings, and composites, to achieve desired characteristics like improved strength, flexibility, or chemical resistance.

Check Digit Verification of cas no

The CAS Registry Mumber 112253-26-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,2,5 and 3 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 112253-26:
(8*1)+(7*1)+(6*2)+(5*2)+(4*5)+(3*3)+(2*2)+(1*6)=76
76 % 10 = 6
So 112253-26-6 is a valid CAS Registry Number.
InChI:InChI=1/C18H20N2O/c21-15-17-8-4-5-9-18(17)20-12-10-19(11-13-20)14-16-6-2-1-3-7-16/h1-9,15H,10-14H2/p+1

112253-26-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-Benzylpiperazin-1-yl)benzaldehyde

1.2 Other means of identification

Product number -
Other names 2-(4-Benzylpiperazino)benzenecarbaldehyde

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:112253-26-6 SDS

112253-26-6Relevant articles and documents

TRPML MODULATORS

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Paragraph 0746, (2021/06/26)

The present invention provides compounds, pharmaceutically acceptable compositions thereof, and methods of using the same.

11C-LABELED BENZYL-LACTAM COMPOUNDS AND THEIR USE AS IMAGING AGENTS

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Page/Page column 23, (2008/06/13)

The invention relates to ""C-labeled compounds, their preparation, compositions comprising an effective amount of a ""C-labeled compound, and the use of a ""C-labeled compound as a radiopharmaceutical for positron emission tomography.

NOVEL BENZYL(IDENE)-LACTAM DERIVATIVES

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Page/Page column 30-31, (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.

A Novel Two-Step Synthesis of Hexahydropyrazinoquinolines

Nijhuis, Walter H. N.,Verboom, Willem,Reinhoudt, David N.

, p. 641 - 645 (2007/10/02)

The hexahydropyrazinoquinolines 2 were prepared in good yields by reaction of 2-(4-substituted 1-piperazinyl)benzaldehydes 5 with malononitrile and subsequent thermal cyclization of the condensation products 6; the latter reaction takes place via a

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