93103-29-8 Usage
Description
5-PYRIDIN-3-YL-1H-IMIDAZOLE-2-THIOL, also known as 3-(2-Mercapto-1H-imidazol-4-yl)pyridine, is a yellow solid compound with the chemical formula C9H7N3S. It is characterized by the presence of a pyridine ring, an imidazole ring, and a thiol group, which contribute to its unique chemical properties and potential applications in various fields.
Uses
Used in Organic Synthesis:
5-PYRIDIN-3-YL-1H-IMIDAZOLE-2-THIOL is used as a synthetic intermediate in the chemical industry for the preparation of various organic compounds. Its unique structure allows it to act as a building block in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 5-PYRIDIN-3-YL-1H-IMIDAZOLE-2-THIOL is used as a key component in the development of new drugs. Its chemical properties make it a promising candidate for the design of novel therapeutic agents with potential applications in various medical fields.
Used in Material Science:
5-PYRIDIN-3-YL-1H-IMIDAZOLE-2-THIOL can also be used in material science for the development of new materials with specific properties. Its ability to form stable complexes with metal ions makes it a potential candidate for the synthesis of metal-organic frameworks (MOFs) and other coordination polymers with applications in catalysis, gas storage, and sensing.
Used in Analytical Chemistry:
In analytical chemistry, 5-PYRIDIN-3-YL-1H-IMIDAZOLE-2-THIOL can be employed as a reagent or a ligand in various analytical techniques. Its affinity for metal ions and other chemical species makes it useful for the development of new methods for the detection and quantification of various analytes.
Overall, 5-PYRIDIN-3-YL-1H-IMIDAZOLE-2-THIOL is a versatile compound with a wide range of potential applications in different industries, including organic synthesis, pharmaceuticals, material science, and analytical chemistry. Its unique chemical properties and structural features make it a valuable asset in the development of new products and technologies.
Check Digit Verification of cas no
The CAS Registry Mumber 93103-29-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,1,0 and 3 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 93103-29:
(7*9)+(6*3)+(5*1)+(4*0)+(3*3)+(2*2)+(1*9)=108
108 % 10 = 8
So 93103-29-8 is a valid CAS Registry Number.
InChI:InChI=1/C8H7N3S/c12-8-10-5-7(11-8)6-2-1-3-9-4-6/h1-5H,(H2,10,11,12)
93103-29-8Relevant articles and documents
Synthesis and Antibacterial Activity of Novel 4″-O-desosaminyl clarithromycin derivatives with 11, 12-arylalkyl side chains
Zhao, Zhe-Hui,Zhu, Di,Zhang, Xiao-Xi,Luo, Zhi-Gang,Lei, Ping-Sheng
, p. 1 - 9 (2018/04/24)
A series of novel 4″-O-desosaminyl clarithromycin derivatives with 11, 12-arylalkyl side chains was synthesized by coupling 6-deoxy-desosamine donors (18, 19) with 4″-OH of compounds 5a–c. The activities of the target compounds were tested against a series of macrolide-sensitive and macrolide-resistant pathogens. Some of them showed activities against macrolide sensitive and resistant pathogens, and compounds 21d and 21e displayed significant improvement of activities against resistant pathogens.
Syntheses of 2-mercapto-4-substituted imidazole derivatives with antiinflammatory properties
Maeda,Suzuki,Iwasaki,Matsumoto,Iwasawa
, p. 2536 - 2543 (2007/10/02)
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