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Thiazolo[4,5-b]pyridin-5(6H)-one, 2,3-dihydro-7-hydroxy-2-(phenylamino)is a chemical compound with the molecular formula C14H12N4O2S. It belongs to the class of thiazole compounds and features a thiazole ring fused to a pyridine ring, with a hydroxy and phenylamino substituent at specific positions. Thiazolo[4,5-b]pyridin-5(6H)-one, 2,3-dihydro-7-hydroxy-2-(phenylamino)has potential biological and pharmaceutical applications, as thiazole derivatives are known for their diverse pharmacological activities, including antimicrobial, antiviral, antitumor, and anti-inflammatory properties. The presence of a hydroxy group and a phenylamino side chain in this chemical structure suggests potential interactions with biological targets, making it a valuable molecule for further pharmaceutical research and development.

70604-16-9

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70604-16-9 Usage

Uses

Used in Pharmaceutical Industry:
Thiazolo[4,5-b]pyridin-5(6H)-one, 2,3-dihydro-7-hydroxy-2-(phenylamino)is used as a pharmaceutical candidate for the development of new drugs due to its potential biological activities and interactions with biological targets.
Used in Antimicrobial Applications:
Thiazolo[4,5-b]pyridin-5(6H)-one, 2,3-dihydro-7-hydroxy-2-(phenylamino)is used as an antimicrobial agent for the treatment of bacterial infections, as thiazole derivatives are known for their antimicrobial properties.
Used in Antiviral Applications:
Thiazolo[4,5-b]pyridin-5(6H)-one, 2,3-dihydro-7-hydroxy-2-(phenylamino)is used as an antiviral agent for the treatment of viral infections, as thiazole derivatives have shown antiviral activity.
Used in Antitumor Applications:
Thiazolo[4,5-b]pyridin-5(6H)-one, 2,3-dihydro-7-hydroxy-2-(phenylamino)is used as an antitumor agent for the treatment of cancer, as thiazole derivatives have demonstrated antitumor properties.
Used in Anti-inflammatory Applications:
Thiazolo[4,5-b]pyridin-5(6H)-one, 2,3-dihydro-7-hydroxy-2-(phenylamino)is used as an anti-inflammatory agent for the treatment of inflammatory conditions, as thiazole derivatives have shown anti-inflammatory properties.

Check Digit Verification of cas no

The CAS Registry Mumber 70604-16-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,6,0 and 4 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 70604-16:
(7*7)+(6*0)+(5*6)+(4*0)+(3*4)+(2*1)+(1*6)=99
99 % 10 = 9
So 70604-16-9 is a valid CAS Registry Number.

70604-16-9Relevant academic research and scientific papers

Synthesis of substituted thiazolo[4,5-b]pyridines and other annulated heterocycles via SN2→Thorpe-Ziegler→Thorpe-Guareschi domino reactions

Shestopalov, Anatoliy M.,Rodinovskaya, Liudmila A.,Shestopalov, Alexander A.

supporting information; experimental part, p. 8945 - 8948 (2011/01/04)

A new combinatorial method for the preparation of substituted thiazolo[4,5-b]pyridines, which utilizes cyanoacetamide, heterocumulenes (isothiocyanates, carbon bisulfide), and ethyl-4-chloroacetoacetate in a new SN2→Thorpe-Ziegler→Thorpe-Guareschi domino reactions has been developed. The obtained thiazolo[4,5-b]pyridines were then used together with aldehydes and malononitrile in another Knoevenagel reaction→Michael reaction→hetero-Thorpe-Ziegler domino reaction for the synthesis of substituted 4,6-dihydro-5H-pyrano[2,3-d]thiazolo[4,5-b]pyridines.

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