Description

N-(2-Cyanopropan-2-yl)acetamide (CAS No. 40652-06-0) is a high-purity organic compound with the molecular formula C₆H₁₀N₂O, widely utilized in pharmaceutical and agrochemical research. This white to off-white crystalline solid exhibits excellent stability under standard conditions, making it ideal for synthetic applications. With an IUPAC name of N-(2-cyanopropan-2-yl)acetamide, it serves as a versatile intermediate in the synthesis of heterocyclic compounds and specialty chemicals. Our product is rigorously tested for purity (typically ≥95% by HPLC) and is supplied with comprehensive analytical documentation, including ¹H NMR and MSDS data. Suitable for laboratory use only.

Properties

• CAS Number: 40652-06-0
• Complexity: 163
• IUPAC Name: N-(1-cyano-1-methyl-ethyl)acetamide
• InChI: InChI=1S/C6H10N2O/c1-5(9)8-6(2,3)4-7/h1-3H3,(H,8,9)
• InChI Key: LKIVSDJTIHCTLP-UHFFFAOYSA-N
• Exact Mass: 126.079312947
• Molecular Formula: C6H10N2O
• Molecular Weight: 126.16
• SMILES: CC(=O)NC(C)(C)C#N
• Topological: 52.9
• Monoisotopic Mass: 126.079312947
• Synonyms: N-(1-Cyano-1-methylethyl)acetamide, Acetamide, N-(1-cyano-1-methylethyl)-, Y6S4KQV46F, NSC 35383, Methyl-2-acetylamino-2 propanenitrile, BRN 1756682, Propionitrile, 2-acetylamino-2-methyl-, NSC-35383, UNII-Y6S4KQV46F, DTXSID70193650, 4-04-00-02620 (Beilstein Handbook Reference), DTXCID10116141, 40652-06-0, n-(2-cyanopropan-2-yl)acetamide, N-(2-Cyano-2-propyl)acetamide, NSC35383, SCHEMBL9055813, QBA65206, MFCD01733809, AKOS009102338, SY173230, DS-001767, CS-0242845, EN300-25603, G22951, Z212046252

Application

N-(2-Cyanopropan-2-yl)acetamide is primarily employed as a key building block in medicinal chemistry for the development of novel bioactive molecules. Researchers utilize this compound in the synthesis of potential enzyme inhibitors and receptor modulators due to its reactive cyano and amide functional groups. It also finds application in crop protection chemical research as a precursor for herbicide intermediates. The compound’s stability allows for flexible reaction conditions in nucleophilic substitution and condensation reactions.

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