122772-20-7 Usage
Description
5-(3,4-DIMETHOXYPHENYL)-4-ETHYL-4H-1,2,4-TRIAZOLE-3-THIOL is a chemical compound belonging to the triazole class, characterized by a molecular formula of C12H14N2O2S. It features a triazole ring fused with a thiol group, along with 3,4-dimethoxyphenyl and ethyl substituents. 5-(3,4-DIMETHOXYPHENYL)-4-ETHYL-4H-1,2,4-TRIAZOLE-3-THIOL may exhibit biological or pharmacological properties due to its unique structure, and it could serve as a precursor in the synthesis of other chemical entities. Further investigation is necessary to explore its full potential and applications.
Uses
Used in Pharmaceutical Industry:
5-(3,4-DIMETHOXYPHENYL)-4-ETHYL-4H-1,2,4-TRIAZOLE-3-THIOL is used as a potential active pharmaceutical ingredient for its possible biological or pharmacological activity. Its unique structure may contribute to the development of new drugs targeting various therapeutic areas.
Used in Agricultural Chemicals:
In the agricultural sector, 5-(3,4-DIMETHOXYPHENYL)-4-ETHYL-4H-1,2,4-TRIAZOLE-3-THIOL may be utilized as a component in the formulation of pesticides or fungicides, leveraging its chemical properties to control or prevent crop diseases and pests.
Used in Materials Science:
5-(3,4-DIMETHOXYPHENYL)-4-ETHYL-4H-1,2,4-TRIAZOLE-3-THIOL could be employed as a building block in the synthesis of new materials with specific properties, such as high-performance polymers or advanced composites, for use in various industries.
Used in Chemical Synthesis:
As a member of the triazole class, 5-(3,4-DIMETHOXYPHENYL)-4-ETHYL-4H-1,2,4-TRIAZOLE-3-THIOL is used as a key intermediate in the synthesis of other complex chemical compounds, potentially leading to the discovery of novel molecules with diverse applications.
Check Digit Verification of cas no
The CAS Registry Mumber 122772-20-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,2,7,7 and 2 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 122772-20:
(8*1)+(7*2)+(6*2)+(5*7)+(4*7)+(3*2)+(2*2)+(1*0)=107
107 % 10 = 7
So 122772-20-7 is a valid CAS Registry Number.
InChI:InChI=1/C12H15N3O2S/c1-4-15-11(13-14-12(15)18)8-5-6-9(16-2)10(7-8)17-3/h5-7H,4H2,1-3H3,(H,14,18)
122772-20-7Relevant articles and documents
1,2,4-Triazole/oxime hybrids as new strategy for nitric oxide donors: Synthesis, anti-inflammatory, ulceroginicity and antiproliferative activities
Abuo-Rahma, Gamal El-Din A.A.,Abdel-Aziz, Mohamed,Beshr, Eman A.M.,Ali, Taha F.S.
, p. 185 - 198 (2014/01/06)
A series of novel nitric oxide (NO) donating triazole/oxime hybrids was prepared and evaluated for their anti-inflammatory activity and antiproliferative activity. Most of the tested compounds showed significant anti-inflammatory activity using carrageenan-induced rat paw edema method compared to indomethacin. Calculation of the ulcer indices and histopathological investigation indicated that the prepared NO-donating oximes exhibited less ulcerogenicity compared to their ketone intermediates and indomethacin. The NO-donating oximes 7i and 7k achieved remarkable cell growth inhibition activity against most of the tested cell lines. Compound 7k was found to be with high selectivity against CNS subpanel with selectivity ratio of 11.99 at GI 50 level.
Synthesis of 5-aryl-3-mercapto-4-substituted-triazoles
Pathak,Devani,Shishoo,Shah
, p. 83 - 86 (2007/10/02)
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