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2-(4-fluorophenyl)-2,3-dihydro-1H-perimidine is a chemical compound with the molecular formula C14H13FN2. It is a derivative of perimidine, a heterocyclic aromatic compound consisting of a six-membered ring with two nitrogen atoms and four carbon atoms. The structure of 2-(4-fluorophenyl)-2,3-dihydro-1H-perimidine features a 4-fluorophenyl group attached to the 2-position of the perimidine ring, and a dihydro group at the 2,3-positions, which indicates the presence of two hydrogen atoms attached to the carbon atoms in the ring. 2-(4-fluorophenyl)-2,3-dihydro-1H-perimidine may have potential applications in various fields, such as pharmaceuticals, agrochemicals, or materials science, due to its unique structure and properties. However, further research and characterization are needed to fully understand its potential uses and effects.

1813-69-0

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1813-69-0 Usage

Heterocyclic compound

Contains a perimidine ring system and a fluorophenyl group

Pharmaceutical research and drug development

Used for its potential pharmacological properties

Anticonvulsant

Potential to prevent or reduce the severity of seizures

Antipsychotic

Potential to treat or alleviate symptoms of psychosis

Neurotransmitter receptor modulation

Ability to affect the activity of neurotransmitter receptors in the brain

Synthesis and characterization

Of interest to researchers in medicinal chemistry and drug discovery.

Check Digit Verification of cas no

The CAS Registry Mumber 1813-69-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,1 and 3 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1813-69:
(6*1)+(5*8)+(4*1)+(3*3)+(2*6)+(1*9)=80
80 % 10 = 0
So 1813-69-0 is a valid CAS Registry Number.

1813-69-0SDS

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-fluorophenyl)-2,3-dihydro-1H-perimidine

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:1813-69-0 SDS

1813-69-0Downstream Products

1813-69-0Relevant academic research and scientific papers

Phosphine-Free Well-Defined Mn(I) Complex-Catalyzed Synthesis of Amine, Imine, and 2,3-Dihydro-1 H-perimidine via Hydrogen Autotransfer or Acceptorless Dehydrogenative Coupling of Amine and Alcohol

Das, Kalicharan,Mondal, Avijit,Pal, Debjyoti,Srivastava, Hemant Kumar,Srimani, Dipankar

supporting information, p. 1815 - 1825 (2019/04/30)

The application of nontoxic, earth-abundant transition metals in place of costly noble metals is a paramount goal in catalysis and is especially interesting if the air- and moisture-stable ligand scaffold is used. Herein, we report the synthesis of amines/imines directly from alcohol and amines via hydrogen autotransfer or acceptorless dehydrogenation catalyzed by well-defined phosphine-free Mn complexes. Both imines and amines can be obtained from the same set of alcohols and amines using the same catalyst, only by tuning the reaction conditions. The amount and nature of the base are found to be a highly important aspect for the observed selectivity. Both the primary and secondary amines have been employed as substrates for the N-alkylation reaction. As a highlight, we showed the chemoselective synthesis of resveratrol derivatives. Furthermore, the Mn-catalyzed dehydrogenative synthesis of structurally important 2,3-dihydro-1H-perimidines has also been demonstrated. Density functional theory calculations were also carried out to model the reaction path and to calculate the reaction profile.

Application of SiO 2 nanoparticles as an efficient catalyst to develop syntheses of perimidines and tetraketones

Alinezhad, Heshmatollah,Ahmadi, Armin,Hajiabbasi, Parvin

, (2019/04/10)

Abstract: In this paper, we explore the catalytic activity of SiO 2 nanoparticles (NPs) as an eco-friendly, efficient and reusable catalyst in the synthesis of 2,3-dihydro-1H-perimidines as well as tetraketones. For tetraketones syntheses, a si

Decoration of β-CD-ZrO on Fe3O4 magnetic nanoparticles as a magnetically, recoverable and reusable catalyst for the synthesis of 2,3-dihydro-1H-perimidines

Amrollahi, Mohammad Ali,Vahidnia, Fatemeh

, p. 7569 - 7581 (2018/09/12)

Abstract: This study focuses on covalent grafting of ZrO to β-CD to prepare an organic–inorganic hybrid material. The synthesised product was successfully linked on the surface of Fe3O4 magnetic nanoparticles and characterized by TGA

(Triazinediyl)bis sulfamic acid-functionalized silica-coated magnetite nanoparticles: Preparation, characterization and application as an efficient catalyst for synthesis of mono-, bis-, tris- and spiro-perimidines

Bodaghifard, Mohammad Ali,Asadbegi, Sajad,Bahrami, Zahra

, p. 365 - 376 (2017/01/10)

(Triazinediyl)bis sulfamic acid-functionalized silica-coated magnetite nanoparticles have been prepared and applicated as an efficient catalyst for synthesis of mono-, bis-, tris- and spiro-perimidines. The desired products have been synthesized in high p

Fe3O4/SiO2/(CH2)3N+Me3Br3- core-shell nanoparticles: A novel catalyst for the solvent-free synthesis of five- and six-membered heterocycles

Farrokhi, Azita,Ghodrati, Keivan,Yavari, Issa

, p. 41 - 46 (2015/02/19)

Functionalized magnetic core-shell nanoparticles [Fe3O4/SiO2/(CH2)3N+Me3Br3-] are prepared by co-precipitation method, characterized by transmission electron microscopy, FT-IR, X-ray diffraction, and vibrating sample magnetometer. The catalytic activity of these nanoparticles was tested in the syntheses of imidazole, benzothiazole, and perimidine derivatives, under solvent-free conditions. The catalyst was readily recycled by the use of an external magnetic field and could be reused five times without significant loss of activity or mass.

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