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5-Hydroxy-4-methyl-1-phenyl-1,2,3-triazole is a chemical compound with the molecular formula C10H9N3O. It is a derivative of the 1,2,3-triazole ring system, which is a five-membered heterocyclic ring containing three nitrogen atoms and two carbon atoms. This particular compound features a hydroxyl group (-OH) at the 5-position, a methyl group (-CH3) at the 4-position, and a phenyl group (C6H5) at the 1-position. It is known for its antioxidant properties and is commonly used as a preservative in various applications, such as in the food and pharmaceutical industries, to prevent spoilage and extend shelf life. The compound is also recognized for its ability to chelate metal ions, which can be beneficial in inhibiting the growth of microorganisms. Due to its chemical structure and properties, 5-hydroxy-4-methyl-1-phenyl-1,2,3-triazole is a versatile molecule with potential applications in a range of industries beyond its traditional use as an antioxidant.

3176-49-6

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3176-49-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3176-49-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,1,7 and 6 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 3176-49:
(6*3)+(5*1)+(4*7)+(3*6)+(2*4)+(1*9)=86
86 % 10 = 6
So 3176-49-6 is a valid CAS Registry Number.

3176-49-6Downstream Products

3176-49-6Relevant academic research and scientific papers

Preparation of Acidic 5-Hydroxy-1,2,3-triazoles via the Cycloaddition of Aryl Azides with β-Ketoesters

Pacifico, Roberta,Destro, Dario,Gillick-Healy, Malachi W.,Kelly, Brian G.,Adamo, Mauro F. A.

, p. 11354 - 11360 (2021)

Herein, a high-yielding cycloaddition reaction of β-ketoesters and azides to provide 1,2,3-triazoles is described. The reactions employing 2-unsubstituted β-ketoesters were found to provide 5-methyl-1,2,3-triazoles, whereas 2-alkyl-substituted β-ketoester

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