10248-89-2 Usage
Description
1,3-(difurfuryl)thiourea is a chemical compound with the molecular formula C12H12N2O2S. It is a thiourea derivative that contains two furfuryl groups, known for its antimicrobial, antioxidant, and anticancer properties. This versatile compound is commonly used in the production of rubber and as a corrosion inhibitor, and has been investigated for its potential applications in pharmaceuticals, agrochemicals, and wastewater treatment processes. Due to its potential health hazards, safety information should be carefully reviewed before handling or using this compound.
Uses
Used in Rubber Industry:
1,3-(difurfuryl)thiourea is used as a vulcanization accelerator for enhancing the production process and improving the properties of rubber materials.
Used in Corrosion Inhibition:
1,3-(difurfuryl)thiourea is used as a corrosion inhibitor to protect metal surfaces from degradation, particularly in industrial applications where metal components are exposed to corrosive environments.
Used in Pharmaceutical Applications:
1,3-(difurfuryl)thiourea is used as a potential therapeutic agent for its antimicrobial, antioxidant, and anticancer properties, and is under investigation for its potential use in treating various diseases and conditions.
Used in Agrochemical Applications:
1,3-(difurfuryl)thiourea is used as a potential active ingredient in agrochemicals for its antimicrobial properties, which can help protect crops from diseases and pests.
Used in Wastewater Treatment:
1,3-(difurfuryl)thiourea is used in research for its ability to chelate metal ions, which could potentially be applied in wastewater treatment processes to remove heavy metals and other contaminants from water systems.
Check Digit Verification of cas no
The CAS Registry Mumber 10248-89-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,2,4 and 8 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 10248-89:
(7*1)+(6*0)+(5*2)+(4*4)+(3*8)+(2*8)+(1*9)=82
82 % 10 = 2
So 10248-89-2 is a valid CAS Registry Number.
InChI:InChI=1/C11H12N2O2S/c16-11(12-7-9-3-1-5-14-9)13-8-10-4-2-6-15-10/h1-6H,7-8H2,(H2,12,13,16)
10248-89-2Relevant articles and documents
Green process development for the synthesis of aliphatic symmetrical N,N'-disubstituted thiourea derivatives in aqueous medium
Jangale, Asha D.,Kumavat, Priyanka P.,Wagh, Yogesh B.,Tayade, Yogesh A.,Mahulikar, Pramod P.,Dalal, Dipak S.
, p. 236 - 244 (2015)
A highly efficient green process for the synthesis of N,N'-disubstituted aliphatic thiourea derivatives using primary aliphatic amines and carbon disulfide in aqueous medium at room temperature via a nonisothiocyanate route is described. This protocol illustrates the rapid preparation of N,N'-disubstituted aliphatic thiourea derivatives in excellent yields with some advantages such as no catalyst and simple workup without any side product formation. Moreover the new route is concise, chromatography-free, and adaptable to pilot-scale preparation.
Synthesis of thioureas in ionic liquid medium
Halimehjani, Azim Ziyaei,Farahbakhsh, Fataneh
, p. 284 - 288 (2013/08/26)
A highly efficient procedure for the synthesis of symmetrical thioureas by means of simple condensation of primary amines and carbon disulfide in 1-butyl-3-methylimidazolium chloride [BMIM][Cl] as a cheap and commercially available ionic liquid is presented. This procedure works for aromatic and aliphatic primary amines and give high to excellent yields of symmetrical thioureas without need for any catalyst or tedious work-up.
1-(Methyldithiocarbonyl)imidazole as thiocarbonyl transfer reagent: A facile one-pot three-component synthesis of 3,5- and 1,3,5-substituted-2- thiohydantoins
Sundaram,Venkatesh,Ila,Junjappa
, p. 251 - 254 (2007/10/03)
An efficient three-component one-pot synthesis of 3,5-and 1,3,5-substituted 2-thiohydantoins employing easily accessible amino acid esters, primary amines and 1-(methyldithiocarbonyl)imidazole as thiocarbonyl transfer reagent has been reported. Georg Thieme Verlag Stuttgart.
