CAS 7228-47-9: 1-(2-Naphthyl)ethanol
Formula:C12H12O
InChI:InChI=1S/C12H12O/c1-9(13)11-7-6-10-4-2-3-5-12(10)8-11/h2-9,13H,1H3
InChI key:InChIKey=AXRKCRWZRKETCK-UHFFFAOYSA-N
SMILES:C(C)(O)C1=CC2=C(C=C1)C=CC=C2
Synonyms:- (±)-α-Methyl-2-naphthalenemethanol
- 1-(2-Naphthalenyl)ethanol
- 1-(2-Naphthyl)-1-ethanol
- 1-(Naphthalen-2-Yl)Ethanol
- 1-(Naphthalen-2-yl)ethan-1-ol
- 1-β-Naphthylethanol
- 2-(1-Hydroxyethyl)Naphthalene
- 2-(Naphthalen-1-Yl)Ethanol
- 2-Naphthalenemethanol, α-methyl-
- Beta-Naphthyl Methyl Carbinol
- Methyl 2-naphthyl carbinol
- See more synonyms
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Found 7 products.
1-(2-Naphthyl)ethanol
CAS:Formula:C12H12OPurity:>98.0%(GC)Color and Shape:White to Almost white powder to crystalMolecular weight:172.231-(2-Naphthyl)ethanol, 97%
CAS:This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.Formula:C12H12OPurity:97%Color and Shape:White, Crystals or powder or crystalline powderMolecular weight:172.231-(2-Naphthyl)ethanol
CAS:1-Naphthyl ethanol is a chromatographic solvent that is used in the reaction rate of lipase. It consists of two hydroxyl groups, one on each naphthalene ring. The hydroxyl groups are separated by a carbonyl group and a sterically hindered boron nitride. This compound is synthesized using triflic acid in methanol and reacts with carbinols to form functional groups. 1-Naphthyl ethanol has been shown to have stereoselective reactions with alkenes and alkynes, which may be due to its ability to form hydrogen bonds.Formula:C12H12OPurity:Min. 95%Color and Shape:PowderMolecular weight:172.22 g/mol1-(Naphthalen-2-yl)ethanol
CAS:Formula:C12H12OPurity:98%Color and Shape:SolidMolecular weight:172.223081-(naphthalen-2-yl)ethan-1-ol
CAS:Purity:99.0%Color and Shape:SolidMolecular weight:172.2270050048828
