41480-75-5 Usage
Uses
Used in Organic Synthesis:
2-Diisopropylaminoethanethiol hydrochloride is used as a reducing agent in organic synthesis for its ability to reduce disulfide bonds in proteins, facilitating the synthesis of various organic compounds.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-Diisopropylaminoethanethiol hydrochloride is used as a reducing agent for the preparation of pharmaceutical drugs, contributing to the development of new medications and improving the synthesis process of existing ones.
Used in Medical Treatments:
2-Diisopropylaminoethanethiol hydrochloride is used as a therapeutic agent in the treatment of certain medical conditions, leveraging its reducing properties to address specific health issues.
Used in Corrosion Inhibition:
As a corrosion inhibitor, 2-Diisopropylaminoethanethiol hydrochloride is applied to protect materials from corrosion, extending their lifespan and improving their performance in various industrial settings.
Used as a Chemical Intermediate:
2-Diisopropylaminoethanethiol hydrochloride also serves as a chemical intermediate in the synthesis of other organic compounds, playing a crucial role in the creation of a wide range of chemical products.
Check Digit Verification of cas no
The CAS Registry Mumber 41480-75-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,4,8 and 0 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 41480-75:
(7*4)+(6*1)+(5*4)+(4*8)+(3*0)+(2*7)+(1*5)=105
105 % 10 = 5
So 41480-75-5 is a valid CAS Registry Number.
InChI:InChI=1/C8H19NS.ClH/c1-7(2)9(5-6-10)8(3)4;/h7-8,10H,5-6H2,1-4H3;1H
41480-75-5Relevant academic research and scientific papers
(2-Hydroxyethyl)diisopropylammonium chloride and its derivatives
Mahmoudkhani, Amir Hossein,Langer, Vratislav
, p. 1163 - 1167 (2007/10/03)
The crystal structure of the title compound, C8H20NO+·-Cl-, (I), and the structures of its derivatives, (2-chloroethyl)diisopropylammonium chloride, C8H19ClN+·Cl-, (II), and diisopropyl(2-mercaptoethyl)ammonium chloride, C8H20NS+·Cl-, (III), are described. The conformations of the isopropyl groups in (II) (gauche-gauche) are different from those in (I) and (III) (both gauche-trans). The structures are stabilized by hydrogen bonds of the type Y-H...Cl (Y = N, O, S) and C-H...X (X = Cl, S).
