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Atomfair Butanamide, 2-amino-3,3-dimethyl- DL-tert-leucine amide C6H14N2O
Description 2-Amino-3,3-dimethylbutanamide (CAS No. 113582-42-6) is a high-purity organic compound with the molecular formula C6H14N2O. This white crystalline solid is a derivative of tert-leucine, featuring an amide functional group, and is widely utilized in pharmaceutical research, peptide synthesis, and as a chiral building block in asymmetric synthesis. With a molecular weight of 130.19 g/mol, it offers excellent stability under standard laboratory conditions. Our product is rigorously tested to ensure ??98% purity (HPLC) and is supplied in sealed packaging to maintain integrity. Ideal for researchers seeking a reliable intermediate for drug discovery or biochemical studies.
Description
Description
2-Amino-3,3-dimethylbutanamide (CAS No. 113582-42-6) is a high-purity organic compound with the molecular formula C6H14N2O. This white crystalline solid is a derivative of tert-leucine, featuring an amide functional group, and is widely utilized in pharmaceutical research, peptide synthesis, and as a chiral building block in asymmetric synthesis. With a molecular weight of 130.19 g/mol, it offers excellent stability under standard laboratory conditions. Our product is rigorously tested to ensure ??98% purity (HPLC) and is supplied in sealed packaging to maintain integrity. Ideal for researchers seeking a reliable intermediate for drug discovery or biochemical studies.
- CAS No: 113582-42-6
- Molecular Formula: C6H14N2O
- Molecular Weight: 130.19
- Exact Mass: 130.110613074
- Monoisotopic Mass: 130.110613074
- IUPAC Name: 2-amino-3,3-dimethylbutanamide
- SMILES: CC(C)(C)C(C(=O)N)N
- Synonyms: 113582-42-6, 2-amino-3,3-dimethylbutanamide, Butanamide, 2-amino-3,3-dimethyl-, dl-tert-leucine amide, tert-Leucinamide, DL-
Application
2-Amino-3,3-dimethylbutanamide serves as a versatile intermediate in medicinal chemistry, particularly in the synthesis of peptidomimetics and chiral catalysts. Its sterically hindered structure makes it valuable for studying enzyme inhibition and modifying peptide conformation. Researchers also employ it in the development of novel pharmaceuticals targeting neurological disorders.
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