Properties
Description
Tosyl-mannose derivatives incorporate para-toluenesulfonyl leaving groups through stable bonds to carbohydrate units, serving as activated intermediates for nucleophilic substitution conjugation chemistry.
Source
Chemical synthesis
Impurities
No visible impurities to the naked eye.
Solubility
This product is soluble in most organic solvents, such as DCM, DMF, DMSO, and THF, and exhibits excellent solubility in water.
Identity
Confirmed by NMR.
Applications
Mannose-tosyl can be used for its potential to function as a versatile sulfonate ester in nucleophilic displacement reactions.