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1H-Pyrazole, 4,5-dihydro-3-(2-naphthalenyl)-1,5-diphenyl- is a complex organic compound belonging to the pyrazole family. It is characterized by a pyrazole ring fused with a dihydro structure, featuring a 2-naphthalenyl group at the 3-position and two phenyl groups at the 1 and 5 positions. 1H-Pyrazole, 4,5-dihydro-3-(2-naphthalenyl)-1,5-diphenyl- is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, as well as in materials science for the development of new functional materials. Its unique structure endows it with specific chemical and physical properties, making it a subject of interest for researchers in organic chemistry and related fields.

2256-23-7

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2256-23-7 Usage

Molecular Structure

1H-Pyrazole, 4,5-dihydro-3-(2-naphthalenyl)-1,5-diphenylconsists of a pyrazole ring with two interconnected aromatic rings, one containing a naphthalene group and the other a diphenyl group.

Type of Compound

It is an organic compound with a complex chemical structure.

Aromaticity

The presence of aromatic rings in its structure suggests that it may have some level of aromaticity.

Chemical Reactivity

Due to the presence of aromatic rings and the complex structure, the compound could potentially exhibit some degree of chemical reactivity.

Biological Activity

The complex structure and aromaticity of the compound may also indicate potential biological activity.

Potential Applications

1H-Pyrazole, 4,5-dihydro-3-(2-naphthalenyl)-1,5-diphenylhas potential applications in pharmaceuticals, materials science, and chemical research.

Further Research

Additional research and testing are needed to determine the specific properties and potential uses of 1H-Pyrazole, 4,5-dihydro-3-(2-naphthalenyl)-1,5-diphenyl- in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 2256-23-7 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, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2256-23:
(6*2)+(5*2)+(4*5)+(3*6)+(2*2)+(1*3)=67
67 % 10 = 7
So 2256-23-7 is a valid CAS Registry Number.

2256-23-7Relevant academic research and scientific papers

A novel mitochondrial targeting fluorescent probe for ratiometric imaging SO2 derivatives in living cells

Wang, Xiao-Bo,Li, Hui-Jing,Chi, Zhenxing,Zeng, Xianshun,Wang, Li-Juan,Cheng, Yun-Fei,Wu, Yan-Chao

, (2019/12/30)

As an important endogenous signaling molecule, SO2 plays a key role in many physiological processes. However, excessive intake of SO2 and its derivatives lead to serious health complications of various diseases. In order to study the role of SO2 and its derivatives in the biological environment, it is of great significance to develop new and effective monitoring methods. Here, a new red emission fluorescent probe (TNPI) based on pyrazoline and hemicyanine dyes for the high selective detection of SO2 derivatives was developed. The probe TNPI showed some advantages such as long emission wavelength (640 nm), obvious color and fluorescence changes after reaction with SO2 derivatives, high selectivity and sensitivity toward SO2 derivatives (detection limit = 80 nM), and large fluorescence emission shift (160 nm) and signal ratio change (from 0.45–445, about 989 times). Intriguingly, the probe was successfully exploited for the fluorescence imaging of SO2 derivatives in the mitochondria of living cells with low cytotoxicity.

Synthesis, spectral studies and antimicrobial activities of some 2-naphthyl pyrazoline derivatives

Sakthinathan,Vanangamudi,Thirunarayanan

experimental part, p. 693 - 700 (2012/07/17)

A series of 2-naphthyl pyrazolines were synthesized by the cyclization of 2-naphthyl chalcones and phenylhydrazine hydrochloride in the presence of sodium acetate. The yields of pyrazoline derivatives are more than 80%. The synthesized pyrazolines were characterized by their physical constants, IR, 1H, 13C and MS spectra. From the IR and NMR spectra the CN (cm-1) stretches, the pyrazoline ring proton chemical shifts (ppm) of δHa, Hb and Hc and also the carbon chemical shifts (ppm) of δCN are correlated with Hammett substituent constants, F and R, and Swain-Lupton's parameters using single and multi-regression analyses. From the results of linear regression analysis, the effect of substituents on the group frequencies has been predicted. The antimicrobial activities of all synthesized pyrazolines have been studied.

KHSO4 · H2O/SiO2-catalyzed, one-pot, solvent-free synthesis of pyrazolines, tetrahydrocarbozoles and indoles using microwave irradiation

Kapoor, Kamal K.,Ganai, Bilal A.,Kumar, Satish,Andotra, Charanjeet S.

, p. 2727 - 2735 (2007/10/03)

A new high-yielding, operationally simple, solvent-free, and mild method for preparation of pyrazolines, tetrahydrocarbazoles, and indoles has been developed using KHSO4 · H2O impregnated on SiO 2. The reactions have been probed under microwave irradiation (MWI), and ultrasonic and thermal conditions, employing different solid supports. The data revealed that KHSO4 · H2O impregnated on SiO2 under MWI provides the best yields in a shorter time under solvent-free reaction conditions. Copyright Taylor & Francis Group, LLC.

Synthesis of 1-substituted 3,5-diaryl-2-pyrazolines by the reaction of α,β-unsaturated ketones with hydrazines

Levai, Albert,Jeko, Jozsef

, p. 111 - 115 (2007/10/03)

1-Acetyl-, 1-propionyl- and 1-phenyl-3,5-diaryl-2-pyrazolines have been synthesized by the reaction of the appropriate α,β-unsaturated ketones with hydrazine or phenylhydrazine in hot acetic acid or propionic acid. Structures of all new 2-pyrazolines 16-4

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