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2-(Butylthio)-4-phenylthiazole is a chemical compound with the molecular formula C13H15NS2, belonging to the thiazole derivative class of organic compounds. It features a five-membered ring structure with sulfur and nitrogen atoms, along with butylthio and phenyl groups that contribute to its unique chemical and physical properties. Known for its potential applications in pharmaceuticals, agrochemicals, and materials science, 2-(Butylthio)-4-phenylthiazole is of significant interest to the scientific community due to its biological activities and potential as a drug candidate.

69390-10-9

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69390-10-9 Usage

Uses

Used in Pharmaceutical Industry:
2-(Butylthio)-4-phenylthiazole is used as a key intermediate in the synthesis of various pharmaceutical compounds for its unique structural features and biological activities. The presence of the thiazole ring, which is known for its diverse pharmacological properties, makes it a valuable component in the development of new drugs.
Used in Agrochemical Industry:
In the agrochemical sector, 2-(Butylthio)-4-phenylthiazole is utilized as a building block in the creation of novel agrochemicals, such as pesticides and herbicides. Its unique chemical properties allow for the design of effective and targeted agrochemicals that can improve crop protection and yield.
Used in Materials Science:
2-(Butylthio)-4-phenylthiazole is employed as a component in the development of advanced materials with specific properties. Its incorporation into materials can lead to improved performance in various applications, such as in sensors, electronic devices, or as part of new composite materials.
Used in Organic Synthesis:
As a thiazole derivative, 2-(Butylthio)-4-phenylthiazole is used as a versatile building block in organic synthesis. Its reactivity and structural features make it suitable for the preparation of a wide range of organic compounds, contributing to the advancement of organic chemistry and the discovery of new molecules with potential applications in various fields.

Check Digit Verification of cas no

The CAS Registry Mumber 69390-10-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,3,9 and 0 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 69390-10:
(7*6)+(6*9)+(5*3)+(4*9)+(3*0)+(2*1)+(1*0)=149
149 % 10 = 9
So 69390-10-9 is a valid CAS Registry Number.

69390-10-9Downstream Products

69390-10-9Relevant academic research and scientific papers

Dithiocarbamates as an efficient intermediate for the synthesis of 2-(alkylsulfanyl)thiazoles in water

Ziyaei Halimehjani, Azim,Hasani, Leila,Ali Alaei,Saidi, Mohammad R.

, p. 883 - 886 (2016/02/05)

A simple, green and high-yielding procedure for the synthesis of 4-substituted-2-(alkylsulfanyl)thiazoles from the reaction of dithiocarbamates and α-halocarbonyl containing compounds in water is described. Also, a one-pot, two-step procedure for the synt

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