5842-00-2 Usage
Uses
Used in Metalworking Fluids and Lubricants Industry:
2-(Butylamino)ethanethiol is used as a corrosion inhibitor and stabilizer for protecting metal surfaces from corrosion and degradation. It functions as a chelating agent, binding to metal ions and preventing them from causing harm to the metal surfaces, thus maintaining the stability and longevity of metalworking fluids and lubricants.
Used in Pharmaceuticals:
In the pharmaceutical industry, 2-(Butylamino)ethanethiol is utilized for its capacity to form stable complexes with metal ions, which can be beneficial in the development of drugs that require metal ion interactions for their therapeutic effects.
Used in Chemical Synthesis:
2-(Butylamino)ethanethiol is also employed in chemical synthesis processes where its ability to chelate metal ions is advantageous for creating specific chemical compounds or improving the efficiency of certain reactions.
Check Digit Verification of cas no
The CAS Registry Mumber 5842-00-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,4 and 2 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5842-00:
(6*5)+(5*8)+(4*4)+(3*2)+(2*0)+(1*0)=92
92 % 10 = 2
So 5842-00-2 is a valid CAS Registry Number.
InChI:InChI=1/C6H15NS/c1-2-3-4-7-5-6-8/h7-8H,2-6H2,1H3/p+1
5842-00-2Relevant articles and documents
Syntheses de β-sultames (thiazetidines-1,2 dioxyde-1,1)
Champseix, A.,Chanet, J.,Etienne, A.,Berre, A. Lemasson, J. C.,Napierala, C.,Vessiere, R.
, p. 463 - 472 (2007/10/02)
β-sultams (1,2-thiazetidine-1,1-dioxides) are easily prepared by 1-halogensulphonyl-2-aminoalkane cyclisation. Two processes based upon this principle have permitted the preparation of many variously N and C-substituted β-sultams. 1) In the first method 1-chlorosulphonyl-2-aminoalkane hydrochlorides, prepared from taurines or β-aminothiols, cyclised in the presence of base. 2) The second process involves the spontaneous cyclisation of 1-fluorosulphonyl-2-aminoalkanes prepared Michael addition of primary amines to 1-fluorosulphonylethene.
