| Identification | More | [Name]
(R)-NOBIN | [CAS]
137848-28-3 | [Synonyms]
R-2'-AMINO-1,1'-BINAPHTHALEN-2-OL
(R)-(+)-2-AMINO-2'-HYDROXY-1,1'-BINAPHTHYL
R-(+)-2-AMINO-2'-HYDROXY-1,1'-BINAPHTYL
(R)-(+)-NOBIN
R-NOBIN
S-2'-AMINO-1,1'-BINAPHTHALEN-2-OL
S-(-)-2-AMINO-2'-HYDROXY-1,1'-BINAPHTYL
(S)-(-)-2-AMINO-2'-HYDROXY-1,2'-BINAPHTHYL
(S)-(-)-NOBIN
S-NOBIN
(R)-(+)-2-AMINO-2'-HYDROXY-1 1'-BINAPHT
(R)-(+)-2-AMINO-2'-HYDOXY-1,1'-BINAPHTHOL
(R)-(-)-2-AMINO-2''-HYDROXY-1,1''-BINAPHTHYL/R-NOBIN
(R)-(+)-NOBIN 99%
R-2'-Amino-1,1'-binaphthalen-2-ol, R-NOBIN | [Molecular Formula]
C20H15NO | [MDL Number]
MFCD01882346 | [Molecular Weight]
285.34 | [MOL File]
137848-28-3.mol |
| Hazard Information | Back Directory | [Chemical Properties]
Red crystal | [Uses]
(R)-(+)-2′-Amino-1,1′-binaphthalen-2-ol may be used as a catalyst in the asymmetric PTC (phase-transfer catalysis) synthesis of α-amino acids. (R)-NOBIN reacts with trans-azobenzene-4,4′-dicarbonyl chloride to form poly(ester-amide)s, which shows backbone light-regulated chiroptical response. | [General Description]
(R)-(+)-2′-Amino-1,1′-binaphthalen-2-ol is a non-symmetrically substituted 1,1′-binaphthalene ligand. |
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