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132814-16-5

6-Phenyl-5-Piperazino-3(2H)-Pyridazinone is a chemical compound that belongs to the class of organic compounds known as piperazines. These are compounds containing a piperazine ring, which is a saturated aliphatic six-member ring with two nitrogen atoms at any adjacent position. It is a specific kind of pyridazinone, a class of compounds characterized by a pyridazinone moiety, which is a pyridazine bearing a ketone group. The chemical structure of this compound includes a phenyl group, which is a six-carbon aromatic ring, attached to the piperazine ring. However, the biological activities, potential uses, and toxicity of this specific compound are not well documented in scientific literature.

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  • 132814-16-5 Structure

  • Basic information

    1. Product Name: 6-PHENYL-5-PIPERAZINO-3(2H)-PYRIDAZINONE
    2. Synonyms: 6-PHENYL-5-PIPERAZINO-3(2H)-PYRIDAZINONE;6-Phenyl-5-piperazin-1-yl-2H-pyridazin-3-one;6-Phenyl-5-(piperazin-1-yl)pyridazin-3(2H)-one;2,3-Dihydro-3-oxo-6-phenyl-5-(piperazin-1-yl)pyridazine, 1-(1,6-Dihydro-6-oxo-3-phenylpyridazin-4-yl)piperazine
    3. CAS NO:132814-16-5
    4. Molecular Formula: C14H16N4O
    5. Molecular Weight: 256.3
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 132814-16-5.mol

  • Chemical Properties

    1. Melting Point: 268-272°C
    2. Boiling Point: °Cat760mmHg
    3. Flash Point: °C
    4. Appearance: /
    5. Density: 1.31g/cm3
    6. Refractive Index: 1.677
    7. Storage Temp.: 2-8°C
    8. Solubility: N/A
    9. CAS DataBase Reference: 6-PHENYL-5-PIPERAZINO-3(2H)-PYRIDAZINONE(CAS DataBase Reference)
    10. NIST Chemistry Reference: 6-PHENYL-5-PIPERAZINO-3(2H)-PYRIDAZINONE(132814-16-5)
    11. EPA Substance Registry System: 6-PHENYL-5-PIPERAZINO-3(2H)-PYRIDAZINONE(132814-16-5)

  • Safety Data

    1. Hazard Codes: Xi,Xn
    2. Statements: 22
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: IRRITANT
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 132814-16-5(Hazardous Substances Data)

132814-16-5 Usage

Uses

Since the biological activities, potential uses, and toxicity of 6-Phenyl-5-Piperazino-3(2H)-Pyridazinone are not well documented, it is not possible to provide a list of its applications based on the provided materials. Further research and investigation would be required to determine its potential uses in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 132814-16-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,8,1 and 4 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 132814-16:
(8*1)+(7*3)+(6*2)+(5*8)+(4*1)+(3*4)+(2*1)+(1*6)=105
105 % 10 = 5
So 132814-16-5 is a valid CAS Registry Number.
InChI:InChI=1/C14H16N4O/c19-13-10-12(18-8-6-15-7-9-18)14(17-16-13)11-4-2-1-3-5-11/h1-5,10,15H,6-9H2,(H,16,19)

132814-16-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-phenyl-4-piperazin-1-yl-1H-pyridazin-6-one

1.2 Other means of identification

Product number -
Other names 6-Phenyl-5-(piperazin-1-yl)pyridazin-3(2H)-one

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:132814-16-5 SDS

132814-16-5Relevant articles and documents

Pyridazines. XV. Synthesis of 6-aryl-5-amino-3(2H)-pyridazinones as potential platelet aggregation inhibitors

Estevez, Isabel,Ravina, Enrique,Sotelo, Eddy

, p. 1421 - 1428 (2007/10/03)

Several 3(2H)-pyridazinones with amino groups at the 5-position of the pyridazine nucleus have been prepared. The 6-aryl-5-halo-3(2H)-pyridazinones obtained from mucochloric and mucobromic acid lead to the corresponding 5- alkylamino-3(2H)-pyridazinones,

PYRIDAZINE DERIVATIVES, IX. SYNTHESIS OF 2H-PYRIDAZIN-3-ONES WITH AROYLPIPERAZINYL GROUPS

Ravina, Enrique,Teran, Carmen,Santana, Lourdes,Garcia, Neftali,Estevez, Isabel

, p. 1967 - 1974 (2007/10/02)

Several 2H-pyridazin-3-ones with phenyl- or 2-furoylpiperazinyl group, have been prepared. 6-Phenyl-5-(N4-aroyl-N1-piperazinyl)-2H-pyridazin-3-ones were obtained by nucleophilic substitution of the chlorine atom of 6-phenyl-5-chloro-

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