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(Phenylhydrazono)acetaldehyde thiosemicarbazone, with the molecular formula C9H12N4S, is a yellow solid chemical compound. It exhibits solubility in organic solvents and slight solubility in water. (phenylhydrazono)acetaldehyde thiosemicarbazone is recognized for its diverse biological activities, such as antiviral, antimicrobial, and antitumor properties. It has been investigated for its potential to inhibit the growth of various cancer cells and its effectiveness as an anti-HIV and antifungal agent. Furthermore, (phenylhydrazono)acetaldehyde thiosemicarbazone has been explored for its chelating capabilities with certain metal ions, suggesting its utility in industrial and environmental applications. As a result, this versatile compound holds promise for a wide array of uses in the medical, industrial, and environmental sectors.

78797-14-5

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78797-14-5 Usage

Uses

Used in Pharmaceutical Applications:
(Phenylhydrazono)acetaldehyde thiosemicarbazone is used as an antitumor agent for its ability to inhibit the growth of various cancer cells. It targets multiple cancer-related pathways, making it a potential candidate for cancer treatment.
Used in Antiviral Applications:
(phenylhydrazono)acetaldehyde thiosemicarbazone is used as an anti-HIV agent due to its potential to inhibit the replication and spread of the virus, offering a new avenue for HIV treatment.
Used in Antimicrobial Applications:
(Phenylhydrazono)acetaldehyde thiosemicarbazone is utilized as an antimicrobial agent, effective against a range of bacteria and fungi, which can be beneficial in the development of new antibiotics and antifungal medications.
Used in Environmental Applications:
As a chelating agent for certain metal ions, (phenylhydrazono)acetaldehyde thiosemicarbazone is used in environmental remediation processes to help remove toxic metals from contaminated sites, contributing to a cleaner and safer environment.
Used in Industrial Applications:
The chelating properties of (phenylhydrazono)acetaldehyde thiosemicarbazone also make it a valuable compound in various industrial processes, where it can be employed to facilitate the separation, purification, or recovery of specific metal ions.

Check Digit Verification of cas no

The CAS Registry Mumber 78797-14-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,7,9 and 7 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 78797-14:
(7*7)+(6*8)+(5*7)+(4*9)+(3*7)+(2*1)+(1*4)=195
195 % 10 = 5
So 78797-14-5 is a valid CAS Registry Number.

78797-14-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name [(Z)-[(2E)-2-(phenylhydrazinylidene)ethylidene]amino]thiourea

1.2 Other means of identification

Product number -
Other names glyoxal 2-phenylhydrazone thiosemicarbazone

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:78797-14-5 SDS

78797-14-5Downstream Products

78797-14-5Relevant academic research and scientific papers

N*-N*-S* Tridentate Ligand System as Potential Antitumor Agents

Antonini, Ippolito,Claudi, Francesco,Cristalli, Gloria,Franchetti, Palmarisa,Grifantini, Mario,Martelli, Sante

, p. 1181 - 1184 (2007/10/02)

Compounds containing an N*-N*-S* tridentate ligand were synthesized and tested for antitumor activity against P-388 lymphocytic leukemia in mice.Of these, only 2,2'-bipyridyl-6-carbothioamide (1a) showed antitumor activity

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