98555-71-6 Usage
Description
5-(2,5-Dichlorophenyl)-1H-tetrazole is a tetrazole derivative with the molecular formula C7H4Cl2N4. It is a five-membered aromatic heterocyclic compound containing four nitrogen atoms and one carbon atom. This chemical compound is utilized in various fields, including pharmaceutical drug development and chemical research, where it serves as a building block for synthesizing other compounds.
Uses
Used in Pharmaceutical Drug Development:
5-(2,5-Dichlorophenyl)-1H-tetrazole is used as a building block for the synthesis of pharmaceutical drugs. Its unique structure and properties make it a valuable component in the creation of new and innovative medications.
Used in Chemical Research:
In the field of chemical research, 5-(2,5-Dichlorophenyl)-1H-tetrazole is employed as a key component in the synthesis of various compounds. Its versatility and reactivity contribute to the advancement of chemical knowledge and the development of new chemical entities.
Used in Anticonvulsant and Antihypertensive Applications:
5-(2,5-Dichlorophenyl)-1H-tetrazole has been studied for its potential anticonvulsant and antihypertensive properties. Its ability to modulate certain physiological processes makes it a promising candidate for the treatment of conditions such as epilepsy and hypertension.
Used in Enzyme Inhibition:
5-(2,5-DICHLOROPHENYL)-1H-TETRAZOLE has also been investigated for its potential to inhibit the enzyme carbonic anhydrase. By blocking the activity of this enzyme, 5-(2,5-Dichlorophenyl)-1H-tetrazole may have applications in the treatment of various diseases and conditions.
Used in Agricultural Industry:
5-(2,5-Dichlorophenyl)-1H-tetrazole has been explored for its potential use in the agricultural industry, specifically for the development of pesticides and herbicides. Its ability to target and control pests and weeds could contribute to more effective and sustainable agricultural practices.
Check Digit Verification of cas no
The CAS Registry Mumber 98555-71-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,5,5 and 5 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 98555-71:
(7*9)+(6*8)+(5*5)+(4*5)+(3*5)+(2*7)+(1*1)=186
186 % 10 = 6
So 98555-71-6 is a valid CAS Registry Number.
InChI:InChI=1/C7H4Cl2N4/c8-4-1-2-6(9)5(3-4)7-10-12-13-11-7/h1-3H,(H,10,11,12,13)
98555-71-6Relevant articles and documents
Green synthesis of the 1-substituted 1H-1, 2, 3, 4-tetrazoles over bifunctional catalyst based on copper intercalated into Mg/Al hydrotalcite modified magnetite nanoparticles
Salimi, Mehri,Zamanpour, Azadeh
, (2020/05/16)
An effective one-pot, convenient process for the synthesis of 1- substituted 1H-tetrazoles from triethyl orthoformate, amines, and sodium azide is described using copper (II) doped and immobilized on functionalized magnetic hydrotalcite (Fe3O4/HT-NH2 CuII) as a novel recyclable catalyst. The application of this catalyst allows the synthesis of a variety of tetrazoles in good to excellent yields in water. The new catalyst was characterized using Fourier transform infrared (FT-IR) spectroscopy, X-ray diffraction (XRD), scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDX), thermogravimetric analysis (TGA), vibration sample magnetometry (VSM) and inductively coupled plasma analysis (ICP-OES). This new procedure offers several advantages such as short operational simplicity, practicability, and applicability to various substrates and the absence of any tedious workup or purification. The loading amount of CuII (doped and immobilized) on functionalized magnetic hydrotalcite was indicated to be 4.66 mmol g?1, obtained from the ICP-OES analysis. Also, the excellent catalytic performance, thermal stability, and separation of the catalyst make it an excellent heterogeneous system and a useful alternative to other heterogeneous catalysts. Also, the catalyst could be magnetically separated and reused six times without significant loss of catalytic activity.
P2O5-SiO2 as an efficient heterogeneous catalyst for the solvent-free synthesis of 1-substituted 1H-1,2,3,4-tetrazoles under conventional and ultrasound irradiation conditions
Habibi, Davood,Nasrollahzadeh, Mahmoud,Mehrabi, Leila,Mostafaee, Samaneh
, p. 725 - 728 (2013/07/26)
1-Substituted 1H-1,2,3,4-tetrazoles were efficiently synthesized from the reaction of primary amines, triethyl orthoformate, and sodium azide in presence of a catalytic amount of P2O5-SiO2 under conventional and ultrasound irradiation in solvent-free conditions. The advantages of this procedure are high yields, relatively short reaction times, ease of product isolation, low cost, and recovery and reusability of the catalyst.
