N-phenyl-2-bromopropionamide
efficient preparation of enantiopure alpha-hydroxyamides from racemic alpha-bromoamides by haloalkane dehalogenase
General
Type : Haloalkane
Chemical_Nomenclature : 2-bromo-N-phenylpropanamide
Canonical SMILES : CC(C(=O)NC1=CC=CC=C1)Br
InChI : InChI=1S\/C9H10BrNO\/c1-7(10)9(12)11-8-5-3-2-4-6-8\/h2-7H,1H3,(H,11,12)
InChIKey : OPPUMGDCQYPOSM-UHFFFAOYSA-N
Other name(s) : 2-Bromo-N-phenylpropionamide || RefChem:467184 || 622-295-0 || 2-Bromo-N-phenylpropanamide || 42308-20-3 || Propanamide, 2-bromo-N-phenyl- || 2-Bromopropananilide || 2-Bromopropionanilide || N-phenyl-2-bromopropionamide || SCHEMBL628621
MW : 228.09
Formula : C9H10BrNO
CAS_number : 94347-34-9
PubChem : 99113
UniChem : OPPUMGDCQYPOSM-UHFFFAOYSA-N
Target
Structures : No structure
Families : Haloalkane_dehalogenase-HLD1
References (1)
| Title : Dynamic Kinetic Resolution Process Employing Haloalkane Dehalogenase - Westerbeek_2011_ACS.Catal_1_1654 |
| Author(s) : Westerbeek A , Szymanski W , Feringa BL , Janssen DB |
| Ref : ACS Catal , 1 :2823 , 2011 |
| Abstract : |
| PubMedSearch : Westerbeek_2011_ACS.Catal_1_1654 |
| PubMedID: |