Description

2-Amino-4-iminoheptafluoropent-2-ene (CAS No. 77953-70-9) is a highly specialized fluorinated organic compound with the molecular formula C₅H₃F₇N₂. This compound, also known by its IUPAC name (E)-1,1,1,3,5,5,5-heptafluoro-4-iminopent-2-en-2-amine, features a unique heptafluorinated structure with both amino and imino functional groups, making it a valuable intermediate in advanced chemical synthesis. Its high fluorine content and reactive sites offer exceptional utility in pharmaceuticals, agrochemicals, and materials science. The compound is supplied as a high-purity reagent (>98%) with detailed analytical certifications (GC-MS, NMR, HPLC) to ensure consistency for research and industrial applications. Store under inert conditions at recommended temperatures to maintain stability.

Properties

• CAS Number: 77953-70-9
• Complexity: 271
• IUPAC Name: (E)-1,1,1,3,5,5,5-heptafluoro-4-imino-pent-2-en-2-amine
• InChI: InChI=1S/C5H3F7N2/c6-1(2(13)4(7,8)9)3(14)5(10,11)12/h13H,14H2/b3-1+,13-2?
• InChI Key: NSPGYANHJLMYBV-YSJZGAJUSA-N
• Exact Mass: 224.01844524
• Molecular Formula: C5H3F7N2
• Molecular Weight: 224.08
• SMILES: C(=C(/C(F)(F)F)N)(C(=N)C(F)(F)F)/F
• Topological: 49.9
• Monoisotopic Mass: 224.01844524
• Synonyms: 2-Amino-4-iminoheptafluoropent-2-ene, 77953-70-9, (E)-1,1,1,3,5,5,5-heptafluoro-4-iminopent-2-en-2-amine, 2-Penten-2-amine,1,1,1,3,5,5,5-heptafluoro-4-imino-, SCHEMBL5704639, NSPGYANHJLMYBV-YSJZGAJUSA-N, MFCD01075246, Perfluoro-4-iminopent-2-en-2-amine, SBB096600, AKOS007930782, AKOS025310004, 2-amino-4-imino-heptafluoropent-2-ene, MS-20278, (2-AMINO)HEPTAFLUORO-4-IMINO-2-PENTENE, (2E)-1,1,1,3,5,5,5-heptafluoro-4-iminopent-2-en-2-ylamine

Application

2-Amino-4-iminoheptafluoropent-2-ene is primarily used as a building block in the synthesis of fluorinated heterocycles and bioactive molecules. Its reactive imino group enables participation in cyclization and condensation reactions, particularly in pharmaceutical research for drug candidates targeting metabolic disorders. The compound’s fluorinated backbone also enhances lipophilicity, making it relevant for agrochemical formulations requiring improved membrane permeability. Researchers leverage its unique structure to develop novel materials with tailored surface properties.

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