2-Naphthoic acid, 98+%, Thermo Scientific Chemicals
2-Naphthoic acid, 98+%, Thermo Scientific Chemicals
Thermo Scientific Chemicals

2-Naphthoic acid, 98+%, Thermo Scientific Chemicals

Have Questions?
Change viewbuttonViewtableView
Quantity:
5 g
25 g
Catalog number L05102.06
also known as L05102-06
Price (USD)/ Each
35.50
-
Add to cart
Quantity:
5 g
Request bulk or custom format
Price (USD)/ Each
35.50
Add to cart
2-Naphthoic acid, 98+%, Thermo Scientific Chemicals
Catalog numberL05102.06
Price (USD)/ Each
35.50
-
Add to cart
Chemical Identifiers
CAS93-09-4
IUPAC Namenaphthalene-2-carboxylic acid
Molecular FormulaC11H8O2
InChI KeyUOBYKYZJUGYBDK-UHFFFAOYSA-N
SMILESOC(=O)C1=CC=C2C=CC=CC2=C1
View more
SpecificationsSpecification SheetSpecification Sheet
Appearance (Color)White to pale cream to pale brown
FormPowder
Assay (Aqueous acid-base Titration)≥98.0 to ≤102.0%
Assay (Silylated GC)≥98.0%
Identification (FTIR)Conforms
2-Naphthoic acid is an unprotected acid undergoes lithiation, e.g. with s-BuLi, by stereospecific 1,4-addition, providing a facile route to 1,2,2-trisubstituted 1,2-dihydronaphthalenes. It is also used as an intermediate in organic synthesis. The fluorescence spectra and electronic absorption of 2-naphthoic acid was studied.

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.

Applications
2-Naphthoic acid is an unprotected acid undergoes lithiation, e.g. with s-BuLi, by stereospecific 1,4-addition, providing a facile route to 1,2,2-trisubstituted 1,2-dihydronaphthalenes. It is also used as an intermediate in organic synthesis. The fluorescence spectra and electronic absorption of 2-naphthoic acid was studied.

Solubility
Soluble in alcohol, diethyl ether, methanol, and ethyl acetate (20 mg/ml). Insoluble in water.

Notes
Keep container tightly closed in a dry and well-ventilated place. Keep away from oxidizing agents.
RUO – Research Use Only

General References:

  1. Han Yu and Gabriela K Popescu. Inhibition of GluN2A-containing N-methyl-D-aspartate receptors by 2-naphthoic acid. Molecular Pharmacology. 2013, 84,(4), 541-550.
  2. Carolina Berdugo-Clavijo et. al. Methanogenic biodegradation of two-ringed polycyclic aromatic hydrocarbons. FEMS Microbiology Ecology. 2012, 81,(1), 124-133.
  3. The unprotected acid undergoes lithiation, e.g. with s-BuLi, by stereospecific 1,4-addition, providing a facile route to 1,2,2-trisubstituted 1,2-dihydronaphthalenes: J. Org. Chem., 61, 5206 (1996).