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(4E)-4-[(4-hydroxyphenyl)amino]methylidene-5-methyl-2-phenyl-2,4-dihydro-3H-pyrazol-3-one is a complex organic molecule characterized by its extended structure, featuring a pyrazolone ring with a methyl and phenyl substituent. (4E)-4-[(4-hydroxyphenyl)amino]methylidene-5-methyl-2-phenyl-2,4-dihydro-3H-pyrazol-3-one also includes an amino group and a hydroxyphenyl group, connected through a methylene group. The presence of phenyl and hydroxyphenyl groups suggests potential biological activity, possibly as an inhibitor or modulator of enzymes or receptors, due to their known interactions with biomolecules. However, further research is necessary to fully comprehend the compound's potential uses and effects.

23711-41-3

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23711-41-3 Usage

Uses

Used in Pharmaceutical Industry:
(4E)-4-[(4-hydroxyphenyl)amino]methylidene-5-methyl-2-phenyl-2,4-dihydro-3H-pyrazol-3-one is used as a potential therapeutic agent for targeting specific enzymes or receptors in the pharmaceutical industry. The presence of phenyl and hydroxyphenyl groups indicates its potential to interact with biomolecules, which could be harnessed for the development of new drugs.
Used in Chemical Research:
In the field of chemical research, (4E)-4-[(4-hydroxyphenyl)amino]methylidene-5-methyl-2-phenyl-2,4-dihydro-3H-pyrazol-3-one serves as a subject for studying the structure-activity relationship of complex organic molecules. Its unique structure and functional groups make it an interesting candidate for exploring new chemical reactions and potential applications in various fields.
Used in Material Science:
(4E)-4-[(4-hydroxyphenyl)amino]methylidene-5-methyl-2-phenyl-2,4-dihydro-3H-pyrazol-3-one may also find applications in material science, particularly in the development of new materials with specific properties. (4E)-4-[(4-hydroxyphenyl)amino]methylidene-5-methyl-2-phenyl-2,4-dihydro-3H-pyrazol-3-one's structure and functional groups could be utilized to create novel materials with tailored characteristics for various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 23711-41-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,7,1 and 1 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 23711-41:
(7*2)+(6*3)+(5*7)+(4*1)+(3*1)+(2*4)+(1*1)=83
83 % 10 = 3
So 23711-41-3 is a valid CAS Registry Number.

23711-41-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (4E)-4-[(4-hydroxyanilino)methylidene]-5-methyl-2-phenylpyrazol-3-one

1.2 Other means of identification

Product number -
Other names 4-(4-hydroxy-anilinomethylene)-5-methyl-2-phenyl-2,4-dihydro-pyrazol-3-one

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:23711-41-3 SDS

23711-41-3Downstream Products

23711-41-3Relevant academic research and scientific papers

Synthesis, antitumor activity and QSAR studies of some 4-aminomethylidene derivatives of edaravone

Markovic, Violeta,Eric, Slavica,Juranic, Zorica D.,Stanojkovic, Tatjana,Joksovic, Ljubinka,Rankovic, Branislav,Kosanic, Marijana,Joksovic, Milan D.

, p. 18 - 27 (2011/04/15)

A series of aminomethylidene derivatives obtained from 4-formyledaravone were synthesized and characterized by IR, NMR and elemental analysis. All the compounds were screened for their antitumor activity. The compound containing 5-phenylpyrazole moiety (3q) exhibited remarkable antitumor activity in in vitro assays, especially against human breast cancer MDA-MB-361 and MDA-MB-453 cell lines. The most important whole-molecule descriptors for antitumor activity on MDA-MB-453 cells belong to the group of quantum-chemical descriptors.

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