60870-43-1 Usage
General Description
4-ALLYL-5-FURAN-2-YL-4H-[1,2,4]TRIAZOLE-3-THIOL is a chemical compound with a complex molecular structure that includes an allyl group, a furan ring, a triazole ring, and a thiol functional group. 4-ALLYL-5-FURAN-2-YL-4H-[1,2,4]TRIAZOLE-3-THIOL has potential applications in pharmaceuticals, agriculture, and materials science due to its diverse chemical properties. It may be used as a building block in the synthesis of new drugs or as an active ingredient in agricultural products. Additionally, its unique structure and reactivity make it suitable for the development of novel materials with specific electronic or biological properties. Further research and development of 4-ALLYL-5-FURAN-2-YL-4H-[1,2,4]TRIAZOLE-3-THIOL could lead to valuable contributions in various fields of science and technology.
Check Digit Verification of cas no
The CAS Registry Mumber 60870-43-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,8,7 and 0 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 60870-43:
(7*6)+(6*0)+(5*8)+(4*7)+(3*0)+(2*4)+(1*3)=121
121 % 10 = 1
So 60870-43-1 is a valid CAS Registry Number.
InChI:InChI=1/C9H9N3OS/c1-2-5-12-8(10-11-9(12)14)7-4-3-6-13-7/h2-4,6H,1,5H2,(H,11,14)
60870-43-1Relevant articles and documents
Synthesis, antioxidant and antitumor activities of some of new cyclobutane containing triazoles derivatives
Koparir, Pelin
, p. 1028 - 1034 (2019/04/04)
Thiosemicarbazides (2a–e) were obtained by the interaction of furan-2-carboxylic acid hydrazide (1) with five different isothiocyanate (RNCS) derivatives. By addition of KOH to the reaction medium, ethyl, allyl, phenyl and benzyl, p-tolyl substituted 1,2,4-triazoles (3a–e) were obtained. 3a–e were dissolved in dry acetone containing K2CO3 in the presence of 2-chloro-1-(3-methyl-3-mesitylcyclobutyl) ethanone (4) to give 3,4,5-trisubstituted 1,2,4-triazole sulfanyl compounds containing a cyclobutane ring (5a–e). The structures of the final compounds were confirmed by elemental analyses, FT-IR, 1H-NMR and 13C-NMR. The antioxidant and antitumor properties of the synthesized compounds were also investigated. Three of the triazole derivatives with p-tolyl, benzyl and phenyl substituents (5c–e) displayed good antioxidant and antitumor activity in comparison to the standards.
