36175-35-6 Usage
Description
4-Cyclopropyl-4H-[1,2,4]triazole is a heterocyclic chemical compound with the molecular formula C5H6N4. It is a triazole derivative and a member of the cyclopropyl group, known for its potential biological activities and therapeutic properties. 4-Cyclopropyl-4H-[1,2,4]triazole is commonly used in pharmaceutical research and drug development, as well as a building block in organic synthesis for creating various other compounds.
Uses
Used in Pharmaceutical Research and Drug Development:
4-Cyclopropyl-4H-[1,2,4]triazole is used as a pharmaceutical compound for its potential biological activities and therapeutic properties. It plays a crucial role in the development of new drugs and medicines.
Used in Organic Synthesis:
4-Cyclopropyl-4H-[1,2,4]triazole is used as a building block in organic synthesis for creating various other compounds. Its unique structure and properties make it a valuable component in the synthesis of a wide range of chemical products.
Used in Antifungal Applications:
4-Cyclopropyl-4H-[1,2,4]triazole is used as an antifungal agent for its potential to combat fungal infections. Its properties have been studied for their effectiveness in treating various fungal-related conditions.
Used in Antibacterial Applications:
4-Cyclopropyl-4H-[1,2,4]triazole is used as an antibacterial agent for its potential to fight bacterial infections. Research has shown that this compound has the ability to inhibit the growth of certain bacteria, making it a promising candidate for antibacterial treatments.
Used in Antiviral Applications:
4-Cyclopropyl-4H-[1,2,4]triazole is used as an antiviral agent for its potential to combat viral infections. Studies have indicated that this compound may have antiviral properties, offering a potential solution for treating various viral diseases.
Overall, 4-Cyclopropyl-4H-[1,2,4]triazole is a versatile chemical compound with diverse potential applications in various industries, particularly in the field of medicine. Its continued research and development promise to unlock new possibilities for its use in treating various health conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 36175-35-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,1,7 and 5 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 36175-35:
(7*3)+(6*6)+(5*1)+(4*7)+(3*5)+(2*3)+(1*5)=116
116 % 10 = 6
So 36175-35-6 is a valid CAS Registry Number.
InChI:InChI=1/C5H7N3/c1-2-5(1)8-3-6-7-4-8/h3-5H,1-2H2
36175-35-6Relevant articles and documents
Synthesis, spectroscopic, thermal and magnetic characterization of novel spin-crossover iron(II) complexes with 4-cyclopropyl-1,2,4-triazole
Soliman, Ahmed A.,Khattab, Mohamed M.,Abdelhady, Hosam H.,?alitro?, Ivan,Linert, Wolfgang
, p. 99 - 105 (2014)
The new bidentate ligand 4-cyclopropyl-1,2,4-triazole (4-C3trz) has been synthesized and used for preparing 1D Fe(II) SCO compounds of the formula [Fe(4-C3trz)3](X)2·nH 2O; where: X = BF4-, n = 3 for compound (1) and X = ClO4-, n = 2 for compound (2). The new complexes (1) and (2) were characterized using elemental analyses, IR-, mass spectroscopy and thermal analysis. The thermally induced spin-crossover behavior of the complexes was inspected by temperature dependent magnetic susceptibility (SQUID) and DSC measurements. The results of magnetic susceptibility (SQUID) and DSC showed abrupt and complete spin transition with a hysteresis loop T ?1/2 = 230/222, T←1/2 = 221/208 K for complex (1) and T?1/2 = 218/193, T ←1/2 = 202/183 K for complex (2) using SQUID/DSC, respectively. The enthalpy and entropy associated with the spin transition (ST) evaluated by DSC results were ΔtransH = +21.6 and +20.4 kJ mol-1 and ΔtransS =+ 97.5 and +105.5 J mol -1 K-1for the (1) and (2), respectively.
