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344:. It is one of the dimers of naphthalene (or literally: dimers of naphthyl). A colorless solid, it has attracted some attention because the
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Pu, Lin (1998). "1,1'-Binaphthyl Dimers, Oligomers, and
Polymers: Molecular Recognition, Asymmetric Catalysis, and New Materials".
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is 14.5 min. at 50 °C. Substituted derivatives of this parent species, e.g.
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can be isolated due to hindered rotation between the two naphthyl subunits. The
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Except where otherwise noted, data are given for materials in their
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332:is an organic compound with the formula (C
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231:C1=CC=C2C(=C1)C=CC=C2C3=CC=CC4=CC=CC=C43
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304:160 °C (320 °F; 433 K)
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314:(at 25 °C , 100 kPa).
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65:1-Naphthalen-1-ylnaphthalene
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424:Aromatic hydrocarbons
419:1-Naphthyl compounds
48:Preferred IUPAC name
28:1,1'-Binaphthyl
276: g·mol
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318:Infobox references
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391:10.1021/cr970463w
326:Chemical compound
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188:CompTox Dashboard
112:Interactive image
16:(Redirected from
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385:(7): 2405–2494.
379:Chemical Reviews
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284:Colorless solid
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247:Chemical formula
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330:1,1'-Binaphthyl
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312:standard state
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56:-Binaphthalene
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300:Melting point
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124:ECHA InfoCard
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354:racemization
346:atropisomers
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71:Identifiers
63:Other names
294:1.299 g/cm
281:Appearance
240:Properties
130:100.009.155
413:Categories
364:References
358:binaphthol
269:Molar mass
176:T87T28S609
99:3D model (
78:CAS Number
18:Binaphthyl
399:11848968
350:halflife
88:604-53-5
352:of the
290:Density
274:254.332
143:PubChem
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224:SMILES
42:Names
156:11789
101:JSmol
395:PMID
167:UNII
387:doi
193:EPA
146:CID
52:1,1
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338:7
336:H
259:H
253:C
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191:(
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54:′
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