1-Phenyl-1H-1,2,3-triazole

95%

Reagent Code: #40258
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CAS Number 1453-81-2

science Other reagents with same CAS 1453-81-2

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Weight 145.1613 g/mol
Formula C₈H₇N₃
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MDL Number MFCD08695353
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1-Phenyl-1H-1,2,3-triazole is widely used in the field of organic synthesis and medicinal chemistry due to its versatile structure. It serves as a key building block in the development of pharmaceuticals, particularly in the design of drugs targeting various diseases, including cancer, bacterial infections, and viral infections. Its triazole ring is known for its stability and ability to interact with biological targets, making it a valuable scaffold in drug discovery. Additionally, it is employed in the synthesis of agrochemicals, such as herbicides and fungicides, due to its effectiveness in inhibiting specific enzymes or pathways in pests. In material science, it is utilized in the creation of polymers and coatings, where its chemical properties enhance durability and performance. Its applications also extend to the field of coordination chemistry, where it acts as a ligand to form complexes with metals, useful in catalysis and sensor development.

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inventory 100mg
10-20 days ฿3,636.00

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1-Phenyl-1H-1,2,3-triazole
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1-Phenyl-1H-1,2,3-triazole is widely used in the field of organic synthesis and medicinal chemistry due to its versatile structure. It serves as a key building block in the development of pharmaceuticals, particularly in the design of drugs targeting various diseases, including cancer, bacterial infections, and viral infections. Its triazole ring is known for its stability and ability to interact with biological targets, making it a valuable scaffold in drug discovery. Additionally, it is employed in the

1-Phenyl-1H-1,2,3-triazole is widely used in the field of organic synthesis and medicinal chemistry due to its versatile structure. It serves as a key building block in the development of pharmaceuticals, particularly in the design of drugs targeting various diseases, including cancer, bacterial infections, and viral infections. Its triazole ring is known for its stability and ability to interact with biological targets, making it a valuable scaffold in drug discovery. Additionally, it is employed in the synthesis of agrochemicals, such as herbicides and fungicides, due to its effectiveness in inhibiting specific enzymes or pathways in pests. In material science, it is utilized in the creation of polymers and coatings, where its chemical properties enhance durability and performance. Its applications also extend to the field of coordination chemistry, where it acts as a ligand to form complexes with metals, useful in catalysis and sensor development.

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