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2-[(3-methylthiophen-2-yl)methylidene]hydrazinecarbothioamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

5425-42-3

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5425-42-3 Usage

Thioamide derivative

It is a compound derived from thioamide, which is a sulfur analog of amide. This gives the molecule its unique chemical properties and reactivity.

Contains a hydrazine group

The presence of a hydrazine group (N2H4) in the molecule contributes to its reactivity and makes it a useful building block in organic synthesis.

Contains a thioamide group

The thioamide group (R-CSNH2) is a key functional group in 2-[(3-methylthiophen-2-yl)methylidene]hydrazinecarbothioamide, providing it with specific reactivity and properties.

Used in organic synthesis

2-[(3-methylthiophen-2-yl)methylidene]hydrazinecarbothioamide is employed as a reagent in organic synthesis, aiding in the formation of various complex molecules.

Used in medicinal chemistry

2-[(3-methylthiophen-2-yl)methylidene]hydrazinecarbothioamide is also used as a building block for the synthesis of pharmaceuticals and bioactive compounds, contributing to the development of new drugs.

Potential antifungal activities

2-[(3-methylthiophen-2-yl)methylidene]hydrazinecarbothioamide has shown potential as an antifungal agent, which could be useful in treating fungal infections.

Potential antimicrobial activities

The compound also exhibits potential antimicrobial properties, making it a candidate for further research in combating bacterial and other microbial infections.

Important for new drug development

The unique chemical structure and properties of 2-[(3-methylthiophen-2-yl)methylidene]hydrazinecarbothioamide make it an important compound for the development of new drugs and biologically active molecules.

Check Digit Verification of cas no

The CAS Registry Mumber 5425-42-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,2 and 5 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5425-42:
(6*5)+(5*4)+(4*2)+(3*5)+(2*4)+(1*2)=83
83 % 10 = 3
So 5425-42-3 is a valid CAS Registry Number.

5425-42-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name [(3-methylthiophen-2-yl)methylideneamino]thiourea

1.2 Other means of identification

Product number -
Other names 3-methyl-thiophene-2-carbaldehyde 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:5425-42-3 SDS

5425-42-3Relevant academic research and scientific papers

New hydrazinothiazole derivatives of usnic acid as potent TDP1 inhibitors

Filimonov, Aleksander S.,Chepanova, Arina A.,Luzina, Olga A.,Zakharenko, Alexandra L.,Zakharova, Olga D.,Ilina, Ekaterina S.,Dyrkheeva, Nadezhda S.,Kuprushkin, Maxim S.,Kolotaev, Anton V.,Khachatryan, Derenik S.,Patel, Jinal,Leung, Ivanhoe K.H.,Chand, Raina,Ayine-Tora, Daniel M.,Reynisson, Johannes,Volcho, Konstantin P.,Salakhutdinov, Nariman F.,Lavrik, Olga I.

, (2019/10/28)

Tyrosyl-DNA phosphodiesterase 1 (Tdp1) is a promising therapeutic target in cancer therapy. Combination chemotherapy using Tdp1 inhibitors as a component can potentially improve therapeutic response to many chemotherapeutic regimes. A new set of usnic acid derivatives with hydrazonothiazole pharmacophore moieties were synthesized and evaluated as Tdp1 inhibitors. Most of these compounds were found to be potent inhibitors with IC50 values in the low nanomolar range. The activity of the compounds was verified by binding experiments and supported by molecular modeling. The ability of the most effective inhibitors, used at non-toxic concentrations, to sensitize tumors to the anticancer drug topotecan was also demonstrated. The order of administration of the inhibitor and topotecan on their synergistic effect was studied, suggesting that prior or simultaneous introduction of the inhibitor with topotecan is the most effective.

Aryl thiosemicarbazones for the treatment of trypanosomatidic infections

Linciano, Pasquale,Moraes, Carolina B.,Alcantara, Laura M.,Franco, Caio H.,Pascoalino, Bruno,Freitas-Junior, Lucio H.,Macedo, Sara,Santarem, Nuno,Cordeiro-da-Silva, Anabela,Gul, Sheraz,Witt, Gesa,Kuzikov, Maria,Ellinger, Bernhard,Ferrari, Stefania,Luciani, Rosaria,Quotadamo, Antonio,Costantino, Luca,Costi, Maria Paola

, p. 423 - 434 (2018/02/14)

Basing on a library of thiadiazole derivatives showing anti-trypanosomatidic activity, we have considered the thiadiazoles opened forms and reaction intermediates, thiosemicarbazones, as compounds of interest for phenotypic screening against Trypanosoma b

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