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2-((Thiazol-2-ylamino)methyl)phenol is a synthetic organic compound characterized by the molecular formula C11H10N2OS. It features a thiazole ring and a phenol group, which endow it with potential biological activities and make it a valuable building block for the synthesis of pharmaceuticals and agrochemicals. This versatile compound has been studied for its antiviral and antimicrobial properties and may also find applications in material development and as a reference standard in chemical analysis.

13159-88-1

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13159-88-1 Usage

Uses

Used in Pharmaceutical and Agrochemical Industries:
2-((Thiazol-2-ylamino)methyl)phenol is used as a building block for the synthesis of various pharmaceuticals and agrochemicals due to its unique chemical structure and potential biological activities.
Used in Antiviral and Antimicrobial Applications:
2-((Thiazol-2-ylamino)methyl)phenol is used as an antiviral and antimicrobial agent, as its thiazole ring and phenol group may contribute to its potential to inhibit the growth and replication of viruses and bacteria.
Used in Material Development:
2-((Thiazol-2-ylamino)methyl)phenol may have potential applications in the development of new materials, given its unique chemical structure and properties.
Used as a Reference Standard in Chemical Analysis:
2-((Thiazol-2-ylamino)methyl)phenol can be used as a reference standard in chemical analysis, providing a benchmark for the identification and quantification of similar compounds in various analytical techniques.

Check Digit Verification of cas no

The CAS Registry Mumber 13159-88-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,1,5 and 9 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 13159-88:
(7*1)+(6*3)+(5*1)+(4*5)+(3*9)+(2*8)+(1*8)=101
101 % 10 = 1
So 13159-88-1 is a valid CAS Registry Number.

13159-88-1Relevant academic research and scientific papers

Synthesis and characterization of new 3,4-dihydro-2H-benzoand naphtho-1,3-oxazine derivatives

Gabbas, A. U. Garin,Ahmad,Zainuddin,Ibrahim

, p. 1304 - 1306 (2016/04/10)

New 1,3-benzoxazine and naphthoxazine monomers were synthesized using a modified step-wise technique in which formaldehyde was replaced with methylene bromide for ring-closure reaction in the last synthetic step. Salicylaldehyde and 2-hydroxy-1-naphthalde

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