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(3-nitrophenyl)(4-phenyl-4,5-dihydro-1H-pyrazol-3-yl)methanone is a complex organic chemical compound characterized by the presence of a nitrophenyl group and a 4-phenyl-4,5-dihydro-1H-pyrazol-3-yl group connected to a methanone moiety. (3-nitrophenyl)(4-phenyl-4,5-dihydro-1H-pyrazol-3-yl)methanone is notable for its potential applications across various fields due to the unique chemical and biological properties conferred by its constituent groups.

7598-96-1

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7598-96-1 Usage

Uses

Used in Organic Synthesis:
(3-nitrophenyl)(4-phenyl-4,5-dihydro-1H-pyrazol-3-yl)methanone is utilized as an intermediate in organic synthesis for the creation of more complex molecules. Its nitrophenyl group allows for a range of chemical reactions, making it a versatile building block for the development of novel organic compounds.
Used in Pharmaceutical Development:
In the pharmaceutical industry, (3-nitrophenyl)(4-phenyl-4,5-dihydro-1H-pyrazol-3-yl)methanone serves as a key component in the design and synthesis of new drugs. The pyrazol-3-yl group can impart specific biological activities, which may contribute to the therapeutic effects of the resulting pharmaceuticals.
Used in Materials Science:
(3-nitrophenyl)(4-phenyl-4,5-dihydro-1H-pyrazol-3-yl)methanone is also employed in materials science for the development of new materials with specialized functions. (3-nitrophenyl)(4-phenyl-4,5-dihydro-1H-pyrazol-3-yl)methanone's complex structure and the properties of its constituent groups can lead to the creation of materials with unique characteristics, such as improved stability or specific interactions with biological systems.
Used in Research and Development:
Due to its intricate structure, (3-nitrophenyl)(4-phenyl-4,5-dihydro-1H-pyrazol-3-yl)methanone is an intriguing subject for research and development in synthetic chemistry. It offers opportunities for chemists to explore new reaction pathways and chemical transformations, potentially leading to advancements in synthetic methodologies and the discovery of new compounds with practical applications.

Check Digit Verification of cas no

The CAS Registry Mumber 7598-96-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,9 and 8 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 7598-96:
(6*7)+(5*5)+(4*9)+(3*8)+(2*9)+(1*6)=151
151 % 10 = 1
So 7598-96-1 is a valid CAS Registry Number.

7598-96-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (3-nitrophenyl)-(4-phenyl-4,5-dihydro-1H-pyrazol-3-yl)methanone

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 -
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More Details:7598-96-1 SDS

7598-96-1Downstream Products

7598-96-1Relevant academic research and scientific papers

Studies on Pyrazolines: Syntheses, Pyrolysis and Reactivity of Some 3-Aroyl-4-aryl-δ2-pyrazolines

Rao, Ch. Bheemasankara,Raju, G. V. Subba,Raju, P. V. Narasimha

, p. 400 - 403 (2007/10/02)

Δ2-Pyrazolines (IIb-i)have been obtained through cycloaddition of diazomethane to chalcones (Ib-i).The structure (II) has been firmed established on the basis of PMR and (13)C NMR data.Pyrolysis and chemical reactivity of II are described.These

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