15886-24-5 Usage
General Description
2-Furancarboxylic acid, 2-[(2-propen-1-ylamino)thioxomethyl]hydrazide is a chemical compound that is used in pharmaceutical research and drug development. It is a hydrazide derivative of furancarboxylic acid and contains a thioxomethyl group attached to an amino group. 2-Furancarboxylic acid, 2-[(2-propen-1-ylaMino)thioxoMethyl]hydrazide has potential applications in the synthesis of new medications and its properties make it a valuable building block for the creation of novel drug candidates. Additionally, it may have other industrial uses such as in the production of specialty chemicals or as a reagent in chemical reactions. Overall, 2-Furancarboxylic acid, 2-[(2-propen-1-ylamino)thioxomethyl]hydrazide is a versatile chemical that has potential for a variety of applications in the pharmaceutical and chemical industries.
Check Digit Verification of cas no
The CAS Registry Mumber 15886-24-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,8,8 and 6 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 15886-24:
(7*1)+(6*5)+(5*8)+(4*8)+(3*6)+(2*2)+(1*4)=135
135 % 10 = 5
So 15886-24-5 is a valid CAS Registry Number.
15886-24-5Relevant 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.
