37597-96-9 Usage
Description
2-Aminoethyl methanethiosulfonate, hydrochloride is a chemical compound with the ability to react specifically and rapidly with thiols to form mixed disulfides. It is a yellow powder and is commonly used in various applications across different industries due to its unique chemical properties.
Uses
Used in Pharmaceutical Industry:
2-Aminoethyl methanethiosulfonate, hydrochloride is used as a probe for studying the structures of various receptor channels, such as the ACh receptor channel, the GABA receptor channel, and lactose permease. Its ability to form mixed disulfides with thiols allows researchers to map the pore-lining regions of these channels, providing valuable insights into their function and potential therapeutic applications.
Used in Research and Development:
In the field of research and development, 2-Aminoethyl methanethiosulfonate, hydrochloride is utilized for its reactivity with thiols to investigate the structural and functional aspects of proteins and other biomolecules. 2-Aminoethyl methanethiosulfonate, hydrochloride can be employed in various experimental setups to study the interactions between thiols and other molecules, contributing to a better understanding of biological processes and the development of novel therapeutic strategies.
Used in Drug Design and Synthesis:
The unique reactivity of 2-Aminoethyl methanethiosulfonate, hydrochloride with thiols makes it a valuable tool in the design and synthesis of new drugs targeting specific receptor channels or proteins. By incorporating this compound into drug molecules, researchers can potentially enhance the selectivity and efficacy of these drugs, leading to improved treatments for various diseases and conditions.
Used in Analytical Chemistry:
2-Aminoethyl methanethiosulfonate, hydrochloride can be employed in analytical chemistry as a reagent for the detection and quantification of thiols in various samples. Its specific reactivity with thiols allows for the selective identification and measurement of these molecules, which can be crucial in understanding the composition and properties of complex biological systems.
Check Digit Verification of cas no
The CAS Registry Mumber 37597-96-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,5,9 and 7 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 37597-96:
(7*3)+(6*7)+(5*5)+(4*9)+(3*7)+(2*9)+(1*6)=169
169 % 10 = 9
So 37597-96-9 is a valid CAS Registry Number.
InChI:InChI=1/C3H9NO2S2.ClH/c1-8(5,6)7-3-2-4;/h2-4H2,1H3;1H
