70400
2-Naphthoic acid
≥97.0% (GC)
Synonym(s):
2-Naphthalenecarboxylic acid
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About This Item
Linear Formula:
C10H7CO2H
CAS Number:
Molecular Weight:
172.18
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
202-217-8
Beilstein/REAXYS Number:
972039
MDL number:
InChI key
UOBYKYZJUGYBDK-UHFFFAOYSA-N
InChI
1S/C11H8O2/c12-11(13)10-6-5-8-3-1-2-4-9(8)7-10/h1-7H,(H,12,13)
SMILES string
OC(=O)c1ccc2ccccc2c1
assay
≥97.0% (GC)
form
powder
mp
180-185 °C, 185-187 °C (lit.)
Storage Class
13 - Non Combustible Solids
wgk
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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L J Fitzgerald et al.
Acta crystallographica. Section C, Crystal structure communications, 49 ( Pt 11), 1952-1958 (1993-11-15)
The structures of 1-naphthoic acid and 2-naphthoic acid have been investigated in order to determine the degree of disorder of the carboxylic acid groups. 1-Naphthoic acid was found to be completely ordered with C--O bond lengths of 1.214 (3) and
Toshiki Furuya et al.
ChemSusChem, 2(7), 645-649 (2009-06-30)
The large pool of cytochrome P450 (P450) open-reading frames identified in genome sequences has attracted much attention as a resource for new oxidation biocatalysts. P450 genes were cloned from genome-sequenced bacteria and coexpressed with putidaredoxin and its reductase genes to
Hui-Kai Huang et al.
Journal of industrial microbiology & biotechnology, 39(1), 55-62 (2011-06-18)
A heat-labile phenolic acid decarboxylase from Candida guilliermondii (an anamorph of Pichia guilliermondii) was purified to homogeneity by simple successive column chromatography within 3 days. The molecular mass was 20 kDa by sodium dodecyl sulfate-polyacrylamide gel electrophoresis and 36 kDa
Blaise Mathias Costa et al.
Neuropharmacology, 62(4), 1730-1736 (2011-12-14)
Over-activation of N-methyl-d-aspartate (NMDA) receptors is critically involved in many neurological conditions, thus there has been considerable interest in developing NMDA receptor antagonists. We have recently identified a series of naphthoic and phenanthroic acid compounds that allosterically modulate NMDA receptors
M J Melancon et al.
Drug metabolism and disposition: the biological fate of chemicals, 10(2), 128-133 (1982-03-01)
Urine was collected from four female rats for 3 days after two subcutaneous injections with 0.3 mg of 2-methyl[8-14C]naphthalene per kg. Of the 14C injected, 55% was found in the urine. The urine was solvent-fractionated into a toluene fraction (4.9%
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