13207-36-8

Usage

Uses

Used in Chemical Research:
4-Octyl-3-Thiosemicarbazide is used as a research compound for its potential applications in the synthesis of more complex compounds or materials. Its structural similarity to other semicarbazides makes it a valuable candidate for studying chemical reactions and properties.
Used in Biochemical Research:
In the field of biochemistry, 4-Octyl-3-Thiosemicarbazide is used as a research compound to explore its interactions with biological molecules and its potential applications in the development of new biochemical processes or products.
Used in Pharmaceutical Development:
Due to its structural characteristics, 4-Octyl-3-Thiosemicarbazide may be used as a starting material or intermediate in the synthesis of pharmaceutical compounds, contributing to the development of new drugs and therapies.
Used in Material Science:
4-Octyl-3-Thiosemicarbazide's potential use in material science could involve its incorporation into the development of new materials with unique properties, such as improved stability, reactivity, or biocompatibility.
Used in Industrial Applications:
In various industries, 4-Octyl-3-Thiosemicarbazide may be used as a chemical intermediate or additive in the production of specialized products, such as coatings, adhesives, or other materials with specific performance characteristics.

InChI:InChI=1/C9H21N3S/c1-2-3-4-5-6-7-8-11-9(13)12-10/h2-8,10H2,1H3,(H2,11,12,13)

Upstream product

• 4430-45-9 n-octylisothiocyanate 

Relevant academic research and scientific papers

Dioxomolybdenum(VI) complexes of S-methyl-5-bromosalicylidene-N-alkyl substituted thiosemicarbazones: Synthesis, catalase inhibition and antioxidant activities

We synthesized a series of S-methyl-5-bromosalicylidene-N-alkyl substituted thiosemicarbazones and their cis-dioxomolybdenum(VI) complexes having long alkyl chains (propyl, butyl, pentyl, hexyl, and octyl) on thioamide nitrogen. The compounds were characterized by using analytical and spectroscopic methods. The structure of the complex with pentyl group (complex 3) as a representative molecule was determined by X-ray single-crystal diffraction method. The free ligand and their dioxomolybdenum(VI) complexes have been tested for in vitro antioxidant capacity by reduction of copper (II) neocuproine (Cu(II)-Nc) using the CUPRAC (CUPric Reducing Antioxidant Capacity) method. The ligands exhibited more potent in vitro antioxidant capacity than that of the complexes. The obtained trolox equivalent antioxidant capacity (TEAC) value of complex 1 (TEACCUPRAC = 0.73) was higher than those of other complexes. Furthermore, the catalase activity and reactive oxygen species (ROS) scavenging ability of the free ligands and their complexes were determined, showing that complex 1 had significant scavenging activity for ROS.

Process for the production of 2-amino-5-mercapto-1,3,4-thiadiazole

2-Amino-5-mercapto-1,3,4-thiadiazoles can be produced in very high yields from thiosemicarbazides and carbon disulfide in aqueous phase by working in the presence of the corresponding ammonium salt of bis-2,5-mercapto-1,3,4-thiadiazole at a temperature above 40° C. Preferably the process is carried out in the presence of the mother liquor from a previous reaction.