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AG19839

4781-83-3 | 2-Iminothiolane HCl

Packsize Purity Availability Price Discounted Price    Quantity
100mg 95% in stock $32.00 $22.00 -   +
250mg 95% in stock $40.00 $28.00 -   +
500mg 95% in stock $80.00 $56.00 -   +
1g 95% in stock $118.00 $82.00 -   +
5g 95% in stock $582.00 $407.00 -   +
25g 95% in stock $2,035.00 $1,424.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AG19839
Chemical Name: 2-Iminothiolane HCl
CAS Number: 4781-83-3
Molecular Formula: C4H8ClNS
Molecular Weight: 137.631
MDL Number: MFCD00039013
SMILES: N=C1CCCS1.Cl
NSC Number: 340007

 

Computed Properties
Complexity: 69.9  
Covalently-Bonded Unit Count: 2  
Heavy Atom Count: 7  
Hydrogen Bond Acceptor Count: 2  
Hydrogen Bond Donor Count: 2  

 

 

Upstream Synthesis Route
  • 2-Iminothiolane hydrochloride, also known as Traut's reagent, is a versatile compound widely used in chemical synthesis due to its unique properties. This compound is a highly reactive reagent that acts as a sulfhydryl modifier, allowing for the specific derivatization of thiol groups in biomolecules such as proteins and peptides. In chemical synthesis, 2-Iminothiolane hydrochloride is commonly used in the modification of thiol-containing compounds to introduce functional groups or labels for various purposes. One of its key applications is in protein chemistry, where it is used to attach molecules of interest to specific thiol groups on proteins, enabling the study of protein structure, function, and interactions.Furthermore, 2-Iminothiolane hydrochloride is valuable in the creation of thiol-reactive crosslinkers, which are essential for the formation of covalent bonds between biomolecules. This reagent plays a crucial role in the development of conjugates for various biochemical analyses, such as enzyme immunoassays and protein labeling techniques.Overall, the unique reactivity of 2-Iminothiolane hydrochloride makes it an indispensable tool in chemical synthesis, particularly in the modification and functionalization of thiol-containing biomolecules for diverse research and industrial applications.
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