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Norepinephrine | CAS:51-41-2
Norepinephrine
  • Name:Norepinephrine
  • CAS:51-41-2
  • Synonyms:(R)-4-(2-Amino-1-hydroxyethyl)-1,2-benzenediol; L-Arterenol; Levarterenol
  • Molecular Formula:C8H11NO3
  • Molecular Weight:169.18
  • EINESC:200-096-6

Description

Properties

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Safety

Symbol(GHS) T+
Hazard Codes R26/27/28
SDS/MSDS S28;S36/37;S45

SDS

Source SDS/MSDS Samples
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Synthetic Route
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Articles
Peer-Reviewed Papers
Amberlyst 15 supported nitrosonium ion as an efficient reagent for regeneration of carbonyl compounds from oximes, hydrazones and semicarbazones.Lakouraj MM, et al. Reactive functional Polymers, 66(9), 910-915 (2006) Solid-phase synthesis of 5-isoxazol-4-yl-[1,2,4] oxadiazoles.Quan C and Kurth M. The Journal of Organic Chemistry, 69(5), 1470-1474 (2004) A mild and selective method for the conversion of oximes into ketones and aldehydes by the use of N-bromophthalimide.Khazaei A, et al. J. Chem. Res. (M), 2004(10), 695-696 (2004) Hypervalent iodine mediated synthesis of di-and tri-substituted isoxazoles via [3+2] cycloaddition of nitrile oxides.Singhal A, et al. Tetrahedron, 57(7), 719-722 (2016) Facile and Chemoselective Microwave-Assisted Cleavage of Oximes to Their Corresponding Carbonyl Compounds Using N,N?-Dibromo-N,N?-1,3-propylene-bis[(4-methylphenyl)sulfonamide] as a Deoximating Reagent.Khazaei A, et al. Synthesis, 2004(17), 2784-2786 (2004) Microwave-assisted chemoselective cleavage of oximes to their corresponding carbonyl compounds using 1, 3-dichloro-5, 5-dimethyl-hydantoin (DCDMH) as a new Deoximating reagent.Khazaei A and Manesh AA. Synthesis, 2005(12), 1929-1931 (2005) Design, synthesis and antibacterial activity of novel N-formylhydroxylamine derivatives as PDF inhibitors.Yin L, et al. Indian J. Chem. B, 50(5), 695-695 (2011)
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