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24523-53-3

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24523-53-3 Usage

Description

1-(2-Furanyl)ethanone [1-(2-furanyl)ethylidene]hydrazone is a chemical compound that belongs to the class of hydrazones. It is derived from 1-(2-furanyl)ethanone and is known for its potential applications in organic synthesis and pharmaceutical research. 1-(2-Furanyl)ethanone [1-(2-furanyl)ethylidene]hydrazone has been studied for its pharmacological activities, such as antimicrobial and antitumor properties, making it a promising candidate for further investigation in drug development and medicinal chemistry.

Uses

Used in Pharmaceutical Research:
1-(2-Furanyl)ethanone [1-(2-furanyl)ethylidene]hydrazone is used as a research compound for its potential pharmacological activities. Its unique structure and properties make it a valuable tool in the development of new drugs and therapies.
Used in Organic Synthesis:
In the field of organic synthesis, 1-(2-Furanyl)ethanone [1-(2-furanyl)ethylidene]hydrazone serves as a key intermediate or building block for the synthesis of more complex molecules. Its reactivity and versatility contribute to the creation of a wide range of chemical products.
Used in Antimicrobial Applications:
1-(2-Furanyl)ethanone [1-(2-furanyl)ethylidene]hydrazone is used as an antimicrobial agent due to its ability to inhibit the growth of various microorganisms. This property makes it a valuable asset in the development of new antibiotics and antifungal agents.
Used in Antitumor Applications:
In the field of oncology, 1-(2-Furanyl)ethanone [1-(2-furanyl)ethylidene]hydrazone is used as an antitumor agent. Its potential to target and inhibit the growth of cancer cells makes it a promising candidate for the development of novel cancer treatments.
Used in Drug Development:
1-(2-Furanyl)ethanone [1-(2-furanyl)ethylidene]hydrazone's structure and properties make it a valuable candidate for drug development. Researchers can use 1-(2-Furanyl)ethanone [1-(2-furanyl)ethylidene]hydrazone as a starting point to design and synthesize new drugs with improved efficacy and selectivity.
Used in Medicinal Chemistry:
In medicinal chemistry, 1-(2-Furanyl)ethanone [1-(2-furanyl)ethylidene]hydrazone is used to study the structure-activity relationship of various biologically active molecules. This knowledge can be applied to optimize the design of new drugs with better pharmacokinetic and pharmacodynamic properties.

Check Digit Verification of cas no

The CAS Registry Mumber 24523-53-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,5,2 and 3 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 24523-53:
(7*2)+(6*4)+(5*5)+(4*2)+(3*3)+(2*5)+(1*3)=93
93 % 10 = 3
So 24523-53-3 is a valid CAS Registry Number.

24523-53-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-acetylfuran azine

1.2 Other means of identification

Product number -
Other names 2-Acetylfuranketazin

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:24523-53-3 SDS

24523-53-3Upstream product

24523-53-3Downstream Products

24523-53-3Relevant articles and documents

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Tsuge,O. et al.

, p. 505 - 508 (1971)

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Reactions of 1,3-dipolar aldazines and ketazines with the dipolarophile dimethyl acetylenedicarboxylate

El-Alali, Abdullah,Al-Kamali, Ahmed S.

, p. 1293 - 1301 (2007/10/03)

The prepared aldazines (aldehyde azines) and ketazines (ketone azines) were allowed to react with 2 mol of the acetylene derivative. The first products formed were pentalene azine derivatives, which in some cases underwent skeletal rearrangment into acycl

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