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[4-(3-methoxyphenyl)-4,5-dihydro-1H-pyrazol-3-yl](phenyl)methanone, also known as TDZD-8, is a synthetic compound derived from the family of pyrazole derivatives. It is recognized for its potential medicinal properties and is frequently utilized in pharmacological research. TDZD-8 exhibits a range of beneficial effects, including anti-inflammatory, antioxidant, and antitumor activities, as well as its potential as a neuroprotective agent. Its unique chemical structure and properties render it a promising candidate for the development of novel drugs to address a broad spectrum of medical conditions.

7598-97-2

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7598-97-2 Usage

Uses

Used in Pharmaceutical Research:
TDZD-8 is used as a therapeutic agent in pharmaceutical research for its potential to treat various diseases. Its multifaceted medicinal properties, such as anti-inflammatory, antioxidant, and antitumor effects, make it a valuable compound for exploring new treatment options.
Used in Anticancer Applications:
In the field of oncology, TDZD-8 is utilized as an anticancer agent, targeting a wide range of malignancies. Its potential to modulate multiple oncological signaling pathways and exhibit synergistic effects with conventional chemotherapeutic drugs enhances its appeal as a candidate for cancer treatment.
Used in Neuroprotection:
TDZD-8 is also used as a neuroprotective agent, leveraging its potential to safeguard the nervous system and mitigate damage from various neurological conditions. Its application in this area holds promise for the development of treatments for neurodegenerative diseases and other conditions affecting the central and peripheral nervous systems.
Used in Drug Development:
Given its diverse medicinal properties, TDZD-8 is employed in the development of new drugs, with the aim of creating novel therapeutic options for an array of medical conditions. Its unique chemical structure and potential for further modification make it an attractive candidate for the design and synthesis of innovative pharmaceutical compounds.
Used in Antioxidant Applications:
TDZD-8 is utilized as an antioxidant agent, capitalizing on its ability to neutralize harmful free radicals and protect cells from oxidative damage. This application is particularly relevant in the context of conditions associated with increased oxidative stress, such as aging, inflammation, and various diseases.
Used in Anti-inflammatory Applications:
As an anti-inflammatory agent, TDZD-8 is employed to alleviate inflammation and reduce the associated pain and swelling. Its application in this area is beneficial for the treatment of various inflammatory conditions, including autoimmune disorders and conditions resulting from injury or infection.

Check Digit Verification of cas no

The CAS Registry Mumber 7598-97-2 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 7 respectively.
Calculate Digit Verification of CAS Registry Number 7598-97:
(6*7)+(5*5)+(4*9)+(3*8)+(2*9)+(1*7)=152
152 % 10 = 2
So 7598-97-2 is a valid CAS Registry Number.

7598-97-2SDS

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 [4-(3-methoxyphenyl)-4,5-dihydro-1H-pyrazol-3-yl]-phenylmethanone

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

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More Details:7598-97-2 SDS

7598-97-2Relevant 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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