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Home  > 2-(Diethylamino)-n-mesitylacetamide hydrochloride

AA10374

1027-14-1 | 2-(Diethylamino)-n-mesitylacetamide hydrochloride

Packsize Purity Availability Price Discounted Price    Quantity
5g 97% 2 weeks $26.00 $19.00 -   +
25g 97% 2 weeks $55.00 $39.00 -   +
100g 97% 2 weeks $148.00 $103.00 -   +
500g 97% 2 weeks $480.00 $336.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AA10374
Chemical Name: 2-(Diethylamino)-n-mesitylacetamide hydrochloride
CAS Number: 1027-14-1
Molecular Formula: C15H25ClN2O
Molecular Weight: 284.8248
MDL Number: MFCD00425887
SMILES: CCN(CC(=O)Nc1c(C)cc(cc1C)C)CC.Cl

 

Upstream Synthesis Route
  • Trimecaine HCl, also known as N,N-dimethyl-3-(phenylmethylamino)propan-1-amine hydrochloride, serves as a valuable tool in chemical synthesis due to its properties and reactivity profile. This compound is frequently employed as a local anesthetic in various pharmaceutical formulations, but its utility extends beyond medical applications into the realm of organic chemistry. In chemical synthesis, Trimecaine HCl can act as a versatile building block for the construction of more complex molecules. Its unique structure, which contains both aromatic and aliphatic moieties, allows it to participate in diverse synthetic transformations. Through functional group interconversions, such as acylation, alkylation, or reduction reactions, the phenyl and amine groups of Trimecaine HCl can be harnessed to introduce new chemical functionalities into a target molecule.Moreover, the presence of a protonable amino group in Trimecaine HCl makes it a suitable candidate for use in reductive amination reactions. By coupling this amine functionality with a carbonyl compound under reducing conditions, chemists can access a wide array of secondary and tertiary amines, thus expanding the structural diversity of their synthetic libraries.Overall, Trimecaine HCl's dual nature as both a local anesthetic and a synthetic building block underscores its importance in chemical synthesis, offering chemists a practical and efficient means to access structurally intricate molecules with diverse applications.
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