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CasNo: 602-09-5
MF: C20H14O2
Appearance: white to beige powder
Chemical Properties |
1,1′-Bi-2-naphthol is a white to yellowish gray crystalline powder. It is known to be soluble in methanol. Store in a cool and dark place at ambient temperatures for best keeping. |
Uses |
1,1'-Bi-2-naphthol is used as a chiral ligand in alkynylation, Diels-Alder and assymmetric Michael addition reactions. |
Synthesis Reference(s) |
Tetrahedron, 48, p. 9483, 1992 DOI: 10.1016/S0040-4020(01)88316-2Tetrahedron Letters, 24, p. 3261, 1983 DOI: 10.1016/S0040-4039(00)88151-4 |
Safety Profile |
1,1'-Bi-2-naphthol is incompatible with oxidizing agents and should not be stored or handled near them. Poison by ingestion and causes skin irritation along with serious eye irritation. When heated to decomposition it emits acrid smoke and irritatingvapors. |
Purification Methods |
Crystallise the binaphthol from toluene or *benzene (10mL/g). When crystallised from chlorobenzene it has m 238o. Its solubility in dioxane is 5%. [Beilstein 6 IV 7020.] |
A study was conducted to demonstrate ort...
An efficient and practical method to dir...
An eco-friendly and direct arylation of ...
Enantioselective oxidation of 2-naphthol...
1,1'-Bi-2-naphtholborane generated from ...
Herein, heterogeneous, inexpensive, meta...
The oxidation of 2-naphthol to 1,1'-bi-2...
A new dinuclear oxidovanadium(V) complex...
The molecule rac-1,1'-binaphthalene-2,2'...
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A high yielding solid-phase dimerisation...
Density functional theory has been appli...
A new preparative method for enantiomeri...
(R)-1,1′-Bi(2-naphthol) ((R)-BINOL) in a...
1,1′-Binaphthyl-2,2′-diol/quinoline (BIN...
The photoinduced regio- and enantioselec...
The synthesis and characterization of 5-...
Naphthols undergo dimerization in the pr...
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Two trinuclear acetate clusters of iron ...
The title reaction yields cis- and trans...
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The racemic mixture of 2,2'-dihydroxy-1,...
A new type of phosphoric acid bearing a ...
The visible-light-induced oxidative homo...
Abstract: It has been reported that β-Mn...
Selective oxidation of benzyl alcohols t...
The invention relates to a method for ef...
naphthalen-2-ylamine
β-naphthol
7H-dibenzo[c,g]carbazole
1,1'-binaphthalene-2,2'-diamine
2-amino-2’-hydroxy-1,1’-binaphthyl
1,1'-bi-2-naphthol
Conditions | Yield |
---|---|
With rac-methylbenzylamine; In methanol; for 48h; Ambient temperature;
|
6 % Chromat. 2 % Chromat. 1 % Chromat. 85% |
naphthalen-2-ylamine
β-naphthol
1,1'-binaphthalene-2,2'-diamine
(R)-2-amino-2'-hydroxy-1,1'-binaphthyl
(S)-(-)-2'-amino-[1,1'-binaphthalene]-2-ol
1,1'-bi-2-naphthol
Conditions | Yield |
---|---|
With benzylamine; copper dichloride; In methanol; for 48h; Yields of byproduct given; Ambient temperature;
|
30% |
With benzylamine; copper dichloride; In methanol; for 48h; Yield given. Title compound not separated from byproducts; Ambient temperature;
|
30% |
1-bromo-2-naphthol
1,1'-thiobis(2-naphthol)
bis-(2-hydroxy-1-naphthyl)disulphide
sodium methylate
perixanthenoxanthene
(±)-1,1′-binaphthyl-2-2′-diyl dibenzoate
2,2'-diacetoxy-1,1'-binaphthyl
9-phenyldibenzo