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- (R)-(+)-2-Amino-2'-hydroxy-1,1'-binaphthyl
(R)-(+)-2-Amino-2'-hydroxy-1,1'-binaphthyl
PRICE INQUIRYCatalog Number
ACM137848283-2
Product Name
(R)-(+)-2-Amino-2'-hydroxy-1,1'-binaphthyl
Structure
![{[CurrentData.Name]}](https://resource.alfachemic.com/structure/137848-28-3.gif)
CAS
137848-28-3
IUPAC Name
1-(2-aminonaphthalen-1-yl)naphthalen-2-ol;
Molecular Weight
285.346g/mol
Molecular Formula
C20H15NO;
Canonical SMILES
C1=CC=C2C(=C1)C=CC(=C2C3=C(C=CC4=CC=CC=C43)O)N;
InChI
InChI=1S/C20H15NO/c21-17-11-9-13-5-1-3-7-15(13)19(17)20-16-8-4-2-6-14(16)10-12-18(20)22/h1-12,22H,21H2;
InChI Key
HIXQCPGXQVQHJP-UHFFFAOYSA-N;
Complexity
384
Covalently-Bonded Unit Count
1
Exact Mass
285.115g/mol
H-Bond Acceptor
2
H-Bond Donor
2
Heavy Atom Count
22
Monoisotopic Mass
285.115g/mol
Rotatable Bond Count
1
Topological Polar Surface Area
46.2A^2
Application
(R)-(+)-2-Amino-2'-hydroxy-1,1'-binaphthyl serves as a versatile catalyst in the field of chemical synthesis. Its primary purpose lies in facilitating the asymmetric phase-transfer catalysis (PTC) synthesis of α-amino acids, a crucial process in organic chemistry. Additionally, this compound, known as (R)-NOBIN, interacts with trans-azobenzene-4,4'-dicarbonyl chloride to produce poly(ester-amide)s, which are notable for their unique backbone light-regulated chiroptical responses. As a non-symmetrically substituted 1,1'-binaphthalene ligand, (R)-(+)-2-Amino-2'-hydroxy-1,1'-binaphthyl also contributes to various advanced material applications.
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