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2256-18-0

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2256-18-0 Usage

Pyrazole Ring

A five-membered ring structure with one nitrogen atom and one pyrrole-like ring, contributing to the compound's unique properties.

Fused Ring System

The presence of a fused five-membered ring structure, which may influence the compound's stability and reactivity.

Derivative of Pyrazole

The compound is derived from the pyrazole structure, which may indicate similar properties or reactivity to other pyrazole derivatives.

Multiple Phenyl Groups

The presence of multiple phenyl groups (C6H5) in the structure, which can influence the compound's physical and chemical properties.

Methoxy Groups

The presence of methoxy (-OCH3) groups in the structure, which can affect the compound's solubility, reactivity, and potential applications in pharmaceuticals or organic synthesis.

Ethenyl Group

The presence of an ethenyl (C=C) group in the structure, which may contribute to the compound's reactivity and potential for further chemical modification.

Potential Applications

Due to its unique structure and the presence of phenyl and methoxy groups, the compound may have potential applications in pharmaceuticals or organic synthesis.

Biological Activities

The compound may exhibit interesting biological activities or properties due to its complex structure, making it a valuable candidate for further study and research.

Check Digit Verification of cas no

The CAS Registry Mumber 2256-18-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,5 and 6 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2256-18:
(6*2)+(5*2)+(4*5)+(3*6)+(2*1)+(1*8)=70
70 % 10 = 0
So 2256-18-0 is a valid CAS Registry Number.

2256-18-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-(4-methoxyphenyl)-3-[(E)-2-(4-methoxyphenyl)ethenyl]-1-phenyl-4,5-dihydro-1H-pyrazole

1.2 Other means of identification

Product number -
Other names 5-(4-Methoxy-phenyl)-3-[(E)-2-(4-methoxy-phenyl)-vinyl]-1-phenyl-4,5-dihydro-1H-pyrazole

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:2256-18-0 SDS

2256-18-0Relevant articles and documents

Second harmonic generation in pyrazoline derivatives of dibenzylideneacetones and chalcone: A combined experimental and theoretical approach

de Araújo, Raiane Sodré,de Alcantara, Aline Moreira,Abeg?o, Luis M.G.,de Souza, Yago Pereira,Brand?o Silva, Ant?nio Carlos,Machado, Rogério,Joatan Rodrigues, José,Rodriguez Pliego, Josefredo,d'Errico, Francesco,Siqueira Valle, Marcelo,de Alencar, Márcio André Rodrigues Cavalcanti

, (2019/11/13)

In this work, we investigate theoretically and experimentally second harmonic generation (SHG) in three pyrazoline compounds, being two derivatives of dibenzylideneacetone (DBA) (C23H20N2 and C25H24N2O2) and one derivative of chalcone (C21H18N2). The compounds were synthesized after two steps employing a Claisen-Schmidt condensation followed by an addition-elimination reaction with phenylhydrazine. All compounds were characterized using NMR, FT-IR, UV-Vis, and XRD. We calculated the first-order hyperpolarizabilities of these molecules using program packages based on the time-dependent Hartree-Fock (TDHF) and density functional theory (DFT). SHG was characterized by Kurtz and Perry's powder method. We observed that these organic crystals present SHG efficiencies up to 5 times larger than the KDP, and we associated these values to their molecular structure and crystalline arrangements. The values obtained experimentally and theoretically evidence that these compounds have good potential for application in electronic devices based on second-order nonlinear responses.

BLUE LIGHT BLOCKLING SYSTEM CONTAINING PYRAZOLINE OR/AND BENZOIC ACID COMPOUNDS

-

Paragraph 0029; 0041-0046, (2019/09/17)

The present invention relates to an blue light blocking system characterized in that the blue light blocking agents possess the structure of a pyrazoline of the formula (I) or/and a phenylacrylic acid of the formula (II). The compounds of formula (I) or / and formula (II) fully cover the range of short-wavelength blue light to protect eyes; it can also selectively absorb long-wavelength blue light, so that the transmitted light can provide a particularly good visual experience to humans. The invention is applicable to products such as optical films, optical lenses, goggles, skin care, lighting devices, paints, adhesives, or panels. These products have a light-colored appearance and the penetrating light provides an excellent visual experience for humans.

Cellulose sulfonic acid as a green, efficient, and reusable catalyst for Nazarov cyclization of unactivated dienones and pyrazoline synthesis

Daneshfar, Zahra,Rostami, Ali

, p. 104695 - 104707 (2015/12/30)

A high yielding, eco-friendly and simple procedure for the synthesis of five membered carbo- and heterocycles through cellulose sulfonic acid (CSA) mediated electrocyclization processes has been developed. Cellulose sulfonic acid (CSA) not only was able to induce the cyclization of "unactivated" dienones generating cyclopentenoids; it was also able to trigger the cyclization of α,β-unsaturated hydrazones giving rise to pyrazolines in excellent yields under green reaction conditions. The ease of catalyst recovery and reusability, short reaction time, simple experimental and work-up procedure; compared to the conventional methods, makes this protocol practical, environmentally friendly and economically desirable. The cellulose-SO3H (CSA) was characterized by FT-IR spectroscopy, powder X-ray diffraction (XRD) and Scanning Electron Microscopy (SEM) analyses, and catalyst stability was judged by thermogravimetry/differential thermal analysis (TG/DTA). The catalyst can be recycled several times without significant loss of catalytic activity.

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