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2-(3,4-Dichlorophenyl)-1-hydrazonecarbothioamide is a chemical compound characterized by the presence of hydrazone and carbothioamide moieties. It is known for its potential applications in various fields, particularly in medicine, due to its biological properties. 2-(3,4-DICHLOROPHENYL)-1-HYDRAZINECARBOTHIOAMIDE's structure allows for the design of molecules with possible antibacterial and antifungal activities. However, it is essential to handle this complex chemical with care due to its potential risks and hazards. Extensive research and studies are often conducted to fully understand its possible uses and effects, as its exact properties can vary. Professional handling is crucial for safety purposes, and its potential uses are still being explored and studied.

13124-09-9

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13124-09-9 Usage

Uses

Used in Pharmaceutical Industry:
2-(3,4-Dichlorophenyl)-1-hydrazonecarbothioamide is used as a potential active pharmaceutical ingredient for the development of new drugs, particularly in the area of antimicrobial agents. Its hydrazone and carbothioamide moieties contribute to its potential antibacterial and antifungal activities, making it a promising candidate for the treatment of various infections.
Used in Research and Development:
In the field of scientific research, 2-(3,4-Dichlorophenyl)-1-hydrazonecarbothioamide is used as a chemical probe for studying the mechanisms of action of various biological processes. Its unique structure allows researchers to investigate its interactions with different molecular targets, which can lead to a better understanding of its potential therapeutic applications.
Used in Material Science:
2-(3,4-Dichlorophenyl)-1-hydrazonecarbothioamide may also find applications in material science, where its chemical properties can be utilized to develop new materials with specific characteristics. For instance, its potential use in the synthesis of novel polymers or as a component in the development of advanced materials with antimicrobial properties could be explored.

Check Digit Verification of cas no

The CAS Registry Mumber 13124-09-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,1,2 and 4 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 13124-09:
(7*1)+(6*3)+(5*1)+(4*2)+(3*4)+(2*0)+(1*9)=59
59 % 10 = 9
So 13124-09-9 is a valid CAS Registry Number.
InChI:InChI=1/C7H7Cl2N3S/c8-5-2-1-4(3-6(5)9)11-12-7(10)13/h1-3,11H,(H3,10,12,13)

13124-09-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(3,4-Dichlorophenyl)-1-hydrazinecarbothioamide

1.2 Other means of identification

Product number -
Other names 2-(3,4-DICHLOROPHENYL)-1-HYDRAZINECARBOTHIOAMIDE

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:13124-09-9 SDS

13124-09-9Relevant academic research and scientific papers

1,2,4-Triazole derivatives as sigma receptor inhibitors

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Page/Page column 10, (2008/12/05)

The invention relates to the use of compounds having pharmacological activity towards the sigma receptor, and more particularly to 1,2,4-triazole derivatives of formula I to processes of preparation of such compounds and to pharmaceutical compositions comprising them.

Antiimplantation Agents: Part I - 1-Arylthiosemicarbazides

Nagarajan, K.,Talwalker, P.K.,Kulkarni, C.L.,Venkateswarlu, A.,Prabhu, S.S.,Nayak, G.V.

, p. 1243 - 1257 (2007/10/02)

Several 1-arylthiosemicarbazides, 2-arylhydrazinothiazolines and 2-arylhydrazinodihydrothiazines have been examined for their antiimplantation activity in rats.Among the active compounds, 4-methyl-1-(3,5-bistrifluoromethylphenyl)thiosemicarbazide (3, C 2696-Go) and the corresponding 4,4-dimethyl (47), ethyl (4), n-butyl (5) and allyl (6) derivatives completely inhibit implantation at doses 10, 3, 20, 20 and 30 mg/kg respectively.The 3,4-dichlorophenyl analogue (32) is effective at a dose of 30 mg/kg. 2-(3,5-Bistrifluoromethylphenyl)hydrazinothiazoline (51) and the corresponding dihydrothiazine (63) show a weaker activity.The biological profile of C 2696-Go has been investigated in detail.It appears to prevent implantation by its antiuterotropic activity and ability to inhibit desiduoma formation.

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