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1-(3-Chlorophenyl)imidazoline-2-thione is a heterocyclic chemical compound with the molecular formula C9H8ClN3S. It features an imidazoline ring and a thione group, which contribute to its biological activity. 1-(3-CHLOROPHENYL)IMIDAZOLINE-2-THIONE has been studied for its potential use in treating various medical conditions, such as cancer and hypertension, and has shown promise as an antimicrobial and antifungal agent. Its versatility has attracted interest in both the pharmaceutical and agricultural industries for its wide range of potential applications.

30192-81-5

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30192-81-5 Usage

Uses

Used in Pharmaceutical Industry:
1-(3-Chlorophenyl)imidazoline-2-thione is used as a pharmaceutical candidate for the development of drugs targeting various medical conditions. Its biological activity makes it a promising agent for treating diseases such as cancer and hypertension.
Used in Anticancer Applications:
In the field of oncology, 1-(3-Chlorophenyl)imidazoline-2-thione is used as a potential anticancer agent. It has been studied for its ability to target and treat various types of cancer, including solid tumors, by modulating signaling pathways and exhibiting synergistic effects when combined with conventional chemotherapeutic drugs.
Used in Antimicrobial Applications:
1-(3-Chlorophenyl)imidazoline-2-thione is used as an antimicrobial agent, demonstrating potential effectiveness against a range of bacteria. Its ability to inhibit bacterial growth makes it a valuable compound for developing new antibiotics and combating antibiotic resistance.
Used in Antifungal Applications:
In the realm of antifungal treatment, 1-(3-Chlorophenyl)imidazoline-2-thione is used as a potential antifungal agent. It has shown promise in inhibiting the growth of various fungi, making it a candidate for the development of new antifungal drugs to treat fungal infections.
Used in Agricultural Industry:
1-(3-Chlorophenyl)imidazoline-2-thione is used in the agricultural industry for its potential as a biopesticide. Its antimicrobial and antifungal properties can be harnessed to protect crops from diseases and pests, thereby increasing crop yields and ensuring food security.

Check Digit Verification of cas no

The CAS Registry Mumber 30192-81-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,1,9 and 2 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 30192-81:
(7*3)+(6*0)+(5*1)+(4*9)+(3*2)+(2*8)+(1*1)=85
85 % 10 = 5
So 30192-81-5 is a valid CAS Registry Number.
InChI:InChI=1/C9H7ClN2S/c10-7-2-1-3-8(6-7)12-5-4-11-9(12)13/h1-6H,(H,11,13)

30192-81-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(3-Chlorophenyl)imidazoline-2-thione

1.2 Other means of identification

Product number -
Other names 3-(3-chlorophenyl)-1H-imidazole-2-thione

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:30192-81-5 SDS

30192-81-5Upstream product

30192-81-5Downstream Products

30192-81-5Relevant academic research and scientific papers

Structure activity relationships in reactivators of organophosphorus inhibited acetylcholinesterase. VII. 1 Aryl 2 hydroxyiminomethyl 3 methylimidazolium iodides

Franchetti,Grifantini,Martelli,Stein

, p. 18 - 22,21,22 (2007/10/05)

A series of 1 aryl 2 hydroxyiminomethyl 3 methylimidazolium iodides, where the aryl group is either phenyl or substituted phenyl, was prepared and tested for their reactivating potency on phosphorylated acetylcholinesterase (AChE) and for anti AChE activity. The in vitro testing revealed that some of the new compounds are good reactivators. Correlations between their structure and biological activities have been attempted.

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