5891-04-3 Usage
Derivative of thiol
2-(hexylamino)ethanethiol is a derivative of thiol, which is a class of compounds containing a sulfhydryl group (-SH).
Hexylamine functional group
The compound contains a hexylamine functional group, which is a six-carbon straight-chain alkyl group attached to a nitrogen atom.
Building block for organic synthesis
2-(hexylamino)ethanethiol is used as a building block for creating various other compounds in organic synthesis.
Corrosion inhibitor in the petroleum industry
2-(hexylamino)ethanethiol is used as a corrosion inhibitor in the petroleum industry, which helps to prevent the corrosion of metal equipment and pipelines.
Potential applications in medicinal chemistry
2-(hexylamino)ethanethiol has potential applications in the field of medicinal chemistry, particularly as a precursor for the synthesis of pharmaceutical drugs.
Unique chemical structure and properties
Due to its unique chemical structure and properties, 2-(hexylamino)ethanethiol is of interest to researchers in various industries for its potential applications.
Check Digit Verification of cas no
The CAS Registry Mumber 5891-04-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,9 and 1 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5891-04:
(6*5)+(5*8)+(4*9)+(3*1)+(2*0)+(1*4)=113
113 % 10 = 3
So 5891-04-3 is a valid CAS Registry Number.
5891-04-3Relevant articles and documents
Synthesis and radiopharmacological study of unsaturated derivatives of cysteamine
Mesnard,Miginiac,Fatome,et al.
, p. 247 - 252 (2007/10/02)
Synthesis of many unsaturated compounds derivated from cysteamine has been carried out in the three series : β-aminothioethers, β-aminothiols and thiazolidines. These products are more or less toxic, compared to corresponding saturated derivates. They generally have a higher radioprotective activity. The three most effective have a dose reduction factor equivalent to that of cysteamine, two of them having a lower toxicity.