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2-(pyridin-2-ylthio)acetohydrazide is a hydrazide derivative characterized by the molecular formula C8H9N3OS. It features a pyridine ring and a thioether group, which contribute to its unique chemical properties and potential applications in various fields.

104496-91-5

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104496-91-5 Usage

Uses

Used in Pharmaceutical Research:
2-(pyridin-2-ylthio)acetohydrazide is utilized as a potential enzyme inhibitor in pharmaceutical research. Its ability to target and modulate the activity of specific enzymes makes it a valuable tool for studying enzyme functions and developing new therapeutic agents.
Used in Biochemistry:
In the field of biochemistry, 2-(pyridin-2-ylthio)acetohydrazide serves as a versatile building block for the synthesis of other organic compounds. Its unique structure allows for the creation of novel molecules with potential applications in various areas, such as drug development and chemical research.
Used in Medicinal Chemistry:
2-(pyridin-2-ylthio)acetohydrazide is employed in medicinal chemistry for the development of new drugs and therapeutic agents. Its activity against various biological targets, including enzymes and other proteins, makes it a promising candidate for the treatment of various diseases and conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 104496-91-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,4,9 and 6 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 104496-91:
(8*1)+(7*0)+(6*4)+(5*4)+(4*9)+(3*6)+(2*9)+(1*1)=125
125 % 10 = 5
So 104496-91-5 is a valid CAS Registry Number.

104496-91-5Relevant academic research and scientific papers

Synthesis of 3-(thiadiazol-2-ylthio-, pyridin-2-ylthio- and benzimidazol-2-ylthio)-2H-1-benzopyran-2-ones

Ahluwalia, V K,Tyagi, Renu,Khurana, Anju

, p. 1097 - 1100 (2007/10/02)

The title compounds have been prepared by the reaction of thiadiazol-2-ylthio-, pyridin-2-ylthio- and benzimidazol-2-ylthioacetic acid hydrazides with o-hydroxybenzaldehydes followed by cyclization of the resultant acetylhydrazones in the presence of PPA.

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