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5381-21-5

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5381-21-5 Usage

Derived from benzothiophene

The compound is based on the benzothiophene structure, which is a fused ring system containing both benzene and thiophene rings.

Widely used in organic synthesis

1-benzothiophene-3-carbaldehyde thiosemicarbazone serves as an important building block or intermediate in the synthesis of various complex organic molecules.

Pharmaceutical research

The compound has potential applications in the development of new drugs due to its biological activities.

Potential biological activities

This compound is known for its possible effects on living organisms, including antimicrobial, antiviral, and antitumor properties.

Antimicrobial properties

1-benzothiophene-3-carbaldehyde thiosemicarbazone can inhibit the growth of microorganisms, such as bacteria and fungi.

Antiviral properties

The compound has shown potential in inhibiting the replication of viruses, which could be useful in treating viral infections.

Antitumor properties

Research has indicated that 1-benzothiophene-3-carbaldehyde thiosemicarbazone may be effective in inhibiting the growth of cancer cells.

Preclinical studies

The compound has demonstrated promising results in laboratory experiments and animal studies, which may lead to further investigation and potential clinical trials.

Fluorescent probe for detecting metal ions

1-benzothiophene-3-carbaldehyde thiosemicarbazone has been studied for its potential use as a probe to detect and measure the presence of various metal ions in biological systems.

Interest in medicinal chemistry

The compound's diverse applications and potential biological activities have made it a subject of interest in the field of medicinal chemistry.

Applications in materials science

1-benzothiophene-3-carbaldehyde thiosemicarbazone may also have potential uses in the development of new materials with unique properties.

Check Digit Verification of cas no

The CAS Registry Mumber 5381-21-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,8 and 1 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 5381-21:
(6*5)+(5*3)+(4*8)+(3*1)+(2*2)+(1*1)=85
85 % 10 = 5
So 5381-21-5 is a valid CAS Registry Number.

5381-21-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name [(Z)-1-benzothiophen-3-ylmethylideneamino]thiourea

1.2 Other means of identification

Product number -
Other names Benzo[b]thiophen-3-carbaldehyd-thiosemicarbazon

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:5381-21-5 SDS

5381-21-5Downstream Products

5381-21-5Relevant articles and documents

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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