CAS 1592-38-7
:2-Naphthalenemethanol
- 2-(Hydroxymethyl)-naphthalene
- 2-Naphthalenearbinol
- 2-Naphthalenemethanol
- 2-Naphthyl methanol
- 2-Naphthylcarbinol
- 2-Naphthylmethan-1-ol
- 2-Naphthylmethanol
- 2-Naphthylmethyl alcohol
- NSC 408615
- Naphthalen-2-Ylmethanol
- Rarechem Al Bd 0094
- β-(Hydroxymethyl)naphthalene
- β-Naphthylcarbinol
- 2-Naphtylmethyl alcohol
- 2-NAPHTHALENEMETHANOL 98%
- Naphthalene-2-methanol
- 2-Naphtylmethanol
- 2-NaphthaleneMethonal
- (2-Naphtyl)methanol
- See more synonyms
2-Naphthalenemethanol
CAS:Formula:C11H10OPurity:>98.0%(GC)Color and Shape:White to Light yellow powder to crystalMolecular weight:158.20(2-Naphthyl)methanol
CAS:(2-Naphthyl)methanolFormula:C11H10OPurity:≥95%Color and Shape: white solidMolecular weight:158.20g/molβ-Naphthylcarbinol-D7
CAS:Controlled ProductApplications β-Naphthylcarbinol-D7 is labeled β-Naphthylcarbinol (N345645) which is an intermediate in the synthesis of 2-Naphthylcarbapenem derivatives with broad spectrum antibiotics with enhanced potency against MRSA.
References Martikainen, L.E., et al.: Euro. J. Pharma. Sci., 47, 996 (2012);Formula:C11D7H3OColor and Shape:NeatMolecular weight:165.24Beta-Naphthylcarbinol
CAS:Controlled ProductApplications β-Naphthylcarbinol is an intermediate in the synthesis of 2-Naphthylcarbapenem derivatives with broad spectrum antibiotics with enhanced potency against MRSA.
References Martikainen, L.E., et al.: Euro. J. Pharma. Sci., 47, 996 (2012);Formula:C11H10OColor and Shape:NeatMolecular weight:158.22-Naphthalenemethanol
CAS:2-Naphthalenemethanol is a chemical compound that belongs to the group of organic compounds. It is one of the simplest aromatic alcohols and has been used as a model for the study of other more complex molecules. 2-Naphthalenemethanol is synthesized by reacting sodium salts with borane-tetrahydrofuran complex in dry diethyl ether. The reaction mechanism involves the formation of an ester linkage between the two naphthalenes, which can then undergo hydrolysis to form an alcohol. 2-Naphthalenemethanol can be converted into its structural analog, naphthalene, via condensation reactions with formaldehyde or ethylene glycol. The chemical properties of 2-naphthalenemethanol have been studied using nuclear magnetic resonance spectroscopy (NMR) and x-ray crystallography, which revealed that it exists as a zwitterion consisting of two covalently
Formula:C11H10OPurity:Min. 98 Area-%Color and Shape:PowderMolecular weight:158.2 g/molRef: 3D-FN14798
Discontinued product







