The 2,6-difluoro substitution enforces steric control and electronic modulation, while the para-bromo group provides a latent handle for further derivatization if required. Amidine functionality is strongly basic and deliberately chosen for target binding and salt formation in medicinal chemistry. This compound is a highly functionalized aryl amidine, combining a halogen-rich aniline-derived aromatic ring with an isopropyl-substituted amidine moiety.
EthaniMidaMide, N-(4-broMo-2,6-difluorophenyl)-N’-(1-Methylethyl)
| CAS No | 2177297-18-4 |
|---|---|
| Molecular Formula | C11H13BrF2N2 |
| Molecular Weight | 291.13 g/mol |
| Synonyms | N-(4-bromo-2,6-difluorophenyl)-N'-propan-2-ylethanimidamide |
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Frequently Asked Questions
The 2,6-difluoro substitution enforces steric control and electronic modulation, while the para-bromo group provides a latent handle for further derivatization if required. Amidine functionality is strongly basic and deliberately chosen for target binding and salt formation in medicinal chemistry. This compound is a highly functionalized aryl amidine, combining a halogen-rich aniline-derived aromatic ring with an isopropyl-substituted amidine moiety.
The CAS number of EthaniMidaMide, N-(4-broMo-2,6-difluorophenyl)-N’-(1-Methylethyl) is 2177297-18-4.
The molecular formula of EthaniMidaMide, N-(4-broMo-2,6-difluorophenyl)-N’-(1-Methylethyl) is C11H13BrF2N2.
The listed molecular weight of EthaniMidaMide, N-(4-broMo-2,6-difluorophenyl)-N’-(1-Methylethyl) is 291.13 g/mol.
The listed synonym or IUPAC name for EthaniMidaMide, N-(4-broMo-2,6-difluorophenyl)-N’-(1-Methylethyl) is N-(4-bromo-2,6-difluorophenyl)-N'-propan-2-ylethanimidamide.