AA02402
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
500mg | 95% | 2 weeks | $747.00 | $523.00 | - + | |
1g | 95% | 2 weeks | $826.00 | $578.00 | - + | |
5g | 95% | 2 weeks | $1,620.00 | $1,134.00 | - + | |
10g | 95% | 2 weeks | $2,215.00 | $1,550.00 | - + |
*All products are for research use only and not intended for human or animal use.
*All prices are in USD.
Catalog Number: | AA02402 |
Chemical Name: | N-(3-Amino-2,6-dimethylphenyl)acetamide |
CAS Number: | 100445-94-1 |
Molecular Formula: | C10H14N2O |
Molecular Weight: | 178.231 |
MDL Number: | MFCD00211070 |
SMILES: | CC(=O)Nc1c(C)ccc(c1C)N |
N-(3-Amino-2,6-dimethylphenyl)acetamide, also known as $name$, is a versatile compound widely utilized in chemical synthesis as a key intermediate. This compound plays a crucial role in various organic reactions, particularly in the production of pharmaceuticals, agrochemicals, and specialty chemicals. Its unique structure and functional groups make it a valuable building block for the synthesis of complex molecules.In chemical synthesis, $name$ is commonly employed as a precursor in the preparation of novel compounds with potential biological activities. Its amino and acetyl groups enable it to participate in diverse synthetic pathways, including amidation, acylation, and nucleophilic substitution reactions. Through strategic manipulation of its functional groups, chemists can effectively modify the molecular structure of $name$ to introduce desired properties and functionalities in the final product.Moreover, the presence of the 3-amino-2,6-dimethylphenyl moiety in $name$ confers specific chemical reactivity and stereochemistry, making it a valuable tool in designing stereoselective synthesis routes. By harnessing the reactivity of this aromatic amine group, chemists can orchestrate selective bond-forming processes to access chiral molecules and enantiopure compounds with high efficiency.Overall, the strategic utilization of N-(3-Amino-2,6-dimethylphenyl)acetamide in chemical synthesis enables the efficient construction of diverse molecular architectures and facilitates the discovery of novel compounds with potential applications in various fields of chemistry and beyond.