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2-(3-Ethyl-phenyl)-thiazole-4-carbaldehyde is a chemical compound characterized by the molecular formula C12H11NOS. It is a thiazole derivative featuring a reactive aldehyde group, which renders it versatile for a range of chemical reactions and synthesis processes. 2-(3-ETHYL-PHENYL)-THIAZOLE-4-CARBALDEHYDE is known for its unique structural and chemical properties, making it a valuable component in various scientific and industrial applications.

885279-08-3

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885279-08-3 Usage

Uses

Used in Pharmaceutical Industry:
2-(3-Ethyl-phenyl)-thiazole-4-carbaldehyde is utilized as a building block for the synthesis of a variety of drugs and pharmaceutical compounds. Its presence in the synthesis process is attributed to its ability to contribute to the development of new therapeutic agents.
Used in Organic Synthesis:
In the field of organic synthesis, 2-(3-Ethyl-phenyl)-thiazole-4-carbaldehyde is employed as a key intermediate for the creation of complex organic molecules. Its reactive aldehyde group facilitates multiple types of chemical reactions, broadening its utility in the synthesis of diverse organic compounds.
Used in Materials Science:
2-(3-Ethyl-phenyl)-thiazole-4-carbaldehyde has potential applications in materials science due to its unique structural properties. It can be incorporated into the development of new materials with specific characteristics, such as improved stability or reactivity.
Used in Antimicrobial Applications:
2-(3-Ethyl-phenyl)-thiazole-4-carbaldehyde has been studied for its potential antimicrobial properties, making it a candidate for use in applications where resistance to microbial growth is required, such as in medical devices or coatings.
Used in Antifungal Applications:
Similarly, 2-(3-ETHYL-PHENYL)-THIAZOLE-4-CARBALDEHYDE has shown promise in antifungal applications, suggesting its use in environments where control of fungal growth is necessary, such as in agriculture or in the preservation of materials susceptible to fungal decay.
Used in Anticancer Research:
2-(3-Ethyl-phenyl)-thiazole-4-carbaldehyde is also being investigated for its potential anticancer properties. Its use in this area is based on the possibility of it contributing to the development of new cancer treatments by targeting specific biological pathways or mechanisms involved in cancer progression.

Check Digit Verification of cas no

The CAS Registry Mumber 885279-08-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,5,2,7 and 9 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 885279-08:
(8*8)+(7*8)+(6*5)+(5*2)+(4*7)+(3*9)+(2*0)+(1*8)=223
223 % 10 = 3
So 885279-08-3 is a valid CAS Registry Number.

885279-08-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(3-ethylphenyl)-1,3-thiazole-4-carbaldehyde

1.2 Other means of identification

Product number -
Other names -

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:885279-08-3 SDS

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