18939-69-0 Usage
Uses
Used in Pharmaceutical and Agricultural Industries:
2-Butylisothiouronium chloride is used as a reagent for the preparation of thioamides and thioureas, which serve as important intermediates in the synthesis of various pharmaceuticals and agricultural chemicals. Its role in the synthesis process is crucial for the development of new compounds with potential therapeutic and pesticidal properties.
Used in Organic Synthesis:
2-Butylisothiouronium chloride is used as a reagent in organic synthesis for its ability to react with a wide range of nucleophiles, facilitating the formation of various chemical compounds and intermediates.
Used in Catalytic and Coordination Chemistry:
Due to its ability to form stable complexes with metal ions, 2-butylisothiouronium chloride is used as a ligand in catalytic and coordination chemistry applications. This allows for the development of new catalysts and coordination compounds with potential applications in various chemical processes.
Used in Laboratory Settings:
2-Butylisothiouronium chloride is used as a reagent in laboratory research and development, where its reactivity and complex-forming properties are harnessed for the synthesis of new compounds and the study of chemical reactions. However, due to its toxic and irritant nature, proper handling and safety precautions are essential when working with 2-butylisothiouronium chloride in laboratory settings.
Check Digit Verification of cas no
The CAS Registry Mumber 18939-69-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,9,3 and 9 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 18939-69:
(7*1)+(6*8)+(5*9)+(4*3)+(3*9)+(2*6)+(1*9)=160
160 % 10 = 0
So 18939-69-0 is a valid CAS Registry Number.
InChI:InChI=1/C5H12N2S.ClH/c1-2-3-4-8-5(6)7;/h2-4H2,1H3,(H3,6,7);1H
18939-69-0Relevant academic research and scientific papers
Wenzel, Thomas J.,Zaia, Joseph
, p. 562 - 567 (1987)
Lanthanide complexes of the formula 4>- (fod, 6,6,7,7,8,8,8-heptafluoro-2,2-dimethyl-3,5-octanedione) are effective organic-soluble nuclear magnetic resonance shift reagents for sulfonium and isothiuronium salts.The shift reagent is formed in solution from Ln(fod)3 and Ag(fod) or K(fod).The selection of Ag(fod) or K(fod) in forming the shift reagent is dependent on the anion of the organic salt.Ag(fod) is more effective with halide salts, whereas K(fod) is preferred with tetrafluoroborate salts.Resolution of diastereotopic hydrogen atoms was observed in the shifted spectra of certain substrates.Enantiomeric resolution was obtained in the spectrum of sec-butylisothiuronium chloride with a chiral shift reagent.The reagents can be employed in solvents such as chloroform and benzene.
