N,N-Diallyl-2-bromoacetamide (CAS 60277-03-4)
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N,N-Diallyl-2-bromoacetamide functions as a reactive compound in experimental applications, participating in the synthesis of various organic compounds. Its mechanism of action involves the introduction of a bromine atom into the molecular structure of target compounds, leading to the formation of new chemical entities. N,N-Diallyl-2-Bromoacetamide is known to undergo nucleophilic substitution reactions, where the bromine atom is substituted for another functional group, resulting in the modification of the compound′s properties. N,N-Diallyl-2-bromoacetamide serves as a reagent for the preparation of diverse organic molecules, contributing to the expansion of chemical libraries and the exploration of structure-activity relationships. Its role in these processes involves the transformation of specific chemical structures, enabling the generation of novel compounds for further investigation.
N,N-Diallyl-2-bromoacetamide (CAS 60277-03-4) References
- Triethylborane-induced bromine atom-transfer radical addition in aqueous media: study of the solvent effect on radical addition reactions. | Yorimitsu, H., et al. 2001. J Org Chem. 66: 7776-85. PMID: 11701036
- Polymer network hole transport layers based on photochemically cross-linkable N'N'-diallyl amide tri-N-substituted triazatruxene monomers. | Hu, G., et al. 2018. RSC Adv. 8: 8580-8585. PMID: 35539859
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
N,N-Diallyl-2-bromoacetamide, 500 mg | sc-331446 | 500 mg | $264.00 |