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About This Item
Linear Formula:
C10H7CH2CO2H
CAS Number:
Molecular Weight:
186.21
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
209-475-0
Beilstein/REAXYS Number:
973396
MDL number:
Assay:
99%
Form:
crystals
InChI key
VIBOGIYPPWLDTI-UHFFFAOYSA-N
InChI
1S/C12H10O2/c13-12(14)8-9-5-6-10-3-1-2-4-11(10)7-9/h1-7H,8H2,(H,13,14)
SMILES string
OC(=O)Cc1ccc2ccccc2c1
assay
99%
form
crystals
mp
141-143 °C (lit.)
Quality Level
Related Categories
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
农药列管产品
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Hiroshi Ikeda et al.
Organic letters, 5(10), 1625-1627 (2003-05-09)
[reaction: see text] 6(A),6(D)-Bispyridinio-appended gamma-cyclodextrin effectively enhanced the excimer fluorescence of 2-naphthylacetate. This increase derived from the increase of formation of the 1:2 complex between the cation-charged gamma-cyclodextrin and 2-naphthylacetate by the electrostatic interaction between the host and the guest.
E Abuin et al.
Journal of colloid and interface science, 283(1), 87-93 (2005-02-08)
A study has been made of the effect of urea upon the hydrolysis of 2-naphthyl acetate (2-NA) catalyzed by lipase from Rhizopus arrhizus in AOT-heptane-water reverse micellar solutions at pH 7. The partition constants, K, of 2-NA between n-heptane and
M V Marsh et al.
Xenobiotica; the fate of foreign compounds in biological systems, 11(10), 655-663 (1981-10-01)
1. 14C-Labelled benzoic acid, salicylic acid and 2-naphthylacetic acid were administered orally to horses, and urinary metabolites investigated by chromatographic and mass spectral techniques. 2. [14C]Benzoic acid (5 mg/kg) was eliminated rapidly in the urine, and quantitatively recovered in 24
Misaki Nakai et al.
Inorganic chemistry, 45(7), 3048-3056 (2006-03-28)
Two new dinuclear Ru(III) complexes containing naphthalene moieties, K[Ru2(dhpta)(mu-O2CCH2-1-naph)2] (1) and K[Ru2(dhpta)(mu-O2CCH2-2-naph)2] (2) (H5dhpta = 1,3-diamino-2-hydroxypropane-N,N,N',N'-tetraacetic acid, naph-1-CH2CO2H = 1-naphthylacetic acid, naph-2-CH2CO2H = 2-naphthylacetic acid), were synthesized. Complex 2 crystallized as an orthorhombic system having a space group of Pbca
V Simeon et al.
Chemico-biological interactions, 87(1-3), 103-107 (1993-06-01)
The heat inactivation of esterases in human and rabbit serum was followed at 50 and 55 degrees C by measuring the decrease of activity with paraoxon, phenylacetate and beta-naphthylacetate as substrates. The rate of inactivation measured with the three substrates
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