31182-22-6 Usage
Uses
Used in Rubber and Polymer Industry:
N,N-Di-sec-butylthiourea is used as an accelerator and vulcanizing agent for the production of rubber and various polymers. It helps to speed up the vulcanization process, resulting in improved product quality and reduced manufacturing time.
Used in Pharmaceutical Synthesis:
N,N-Di-sec-butylthiourea is used as an intermediate in the synthesis of pharmaceuticals. Its unique chemical properties make it a valuable component in the development of new drugs and medications.
Used in Agrochemical Synthesis:
N,N-Di-sec-butylthiourea is also used as an intermediate in the synthesis of agrochemicals, contributing to the creation of innovative products for agricultural applications.
Used in Medicinal Chemistry Research:
Due to its potential antioxidant and anti-inflammatory properties, N,N-Di-sec-butylthiourea is a subject of interest in the field of medicinal chemistry. Researchers are exploring its potential applications in the development of new therapeutic agents and treatments for various diseases and conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 31182-22-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,1,8 and 2 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 31182-22:
(7*3)+(6*1)+(5*1)+(4*8)+(3*2)+(2*2)+(1*2)=76
76 % 10 = 6
So 31182-22-6 is a valid CAS Registry Number.
31182-22-6Relevant academic research and scientific papers
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.
