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2-Bromo-5-(4-chlorophenyl)-1,3,4-thiadiazole is a chemical compound characterized by its unique molecular structure, which consists of a thiadiazole ring system with a bromine atom at the 2nd position and a 4-chlorophenyl group at the 5th position. This halogenated heterocyclic compound is known for its potential applications in various chemical and pharmaceutical industries, such as the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals. Due to the presence of both bromine and chlorine atoms, 2-bromo-5-(4-chlorophenyl)-1,3,4-thiadiazole exhibits interesting reactivity and properties that can be exploited in various chemical transformations. Its molecular formula is C4H2BrClN2S, and it has a molecular weight of approximately 240.47 g/mol. The compound's structure and properties make it a valuable intermediate in the synthesis of more complex molecules, contributing to its significance in the field of organic chemistry.

57709-58-7

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57709-58-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 57709-58-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,7,0 and 9 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 57709-58:
(7*5)+(6*7)+(5*7)+(4*0)+(3*9)+(2*5)+(1*8)=157
157 % 10 = 7
So 57709-58-7 is a valid CAS Registry Number.

57709-58-7Relevant academic research and scientific papers

COMPOUND AND ORGANIC LIGHT EMITTING DEVICE COMPRISING SAME

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Paragraph 0226-0229, (2021/01/29)

The present specification provides a compound represented by chemical formula 1 and an organic light emitting device including the same. The compound may improve lifespan characteristics of the organic light emitting device.

From Sphingosine Kinase to Dihydroceramide Desaturase: A Structure-Activity Relationship (SAR) Study of the Enzyme Inhibitory and Anticancer Activity of 4-((4-(4-Chlorophenyl)thiazol-2-yl)amino)phenol (SKI-II)

Aurelio, Luigi,Scullino, Carmen V.,Pitman, Melissa R.,Sexton, Anna,Oliver, Victoria,Davies, Lorena,Rebello, Richard J.,Furic, Luc,Creek, Darren J.,Pitson, Stuart M.,Flynn, Bernard L.

, p. 965 - 984 (2016/02/23)

The sphingosine kinase (SK) inhibitor, SKI-II, has been employed extensively in biological investigations of the role of SK1 and SK2 in disease and has demonstrated impressive anticancer activity in vitro and in vivo. However, interpretations of results u

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