N8505
1-Naphthyl acetate
≥98% (C)
Sinónimos:
α-Naphthyl acetate
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Fórmula lineal:
CH3CO2C10H7
Número CAS:
Peso molecular:
186.21
UNSPSC Code:
12352202
NACRES:
NA.77
PubChem Substance ID:
EC Number:
212-599-8
Beilstein/REAXYS Number:
2046403
MDL number:
Assay:
≥98% (C)
Form:
crystals
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Permítanos ayudarleInChI key
VGKONPUVOVVNSU-UHFFFAOYSA-N
InChI
1S/C12H10O2/c1-9(13)14-12-8-4-6-10-5-2-3-7-11(10)12/h2-8H,1H3
SMILES string
CC(=O)Oc1cccc2ccccc12
assay
≥98% (C)
form
crystals
mp
43-46 °C (lit.)
storage temp.
−20°C
Quality Level
General description
1-Naphthyl acetate is a 1-napthyl ester. Mechanism of photo-Fries rearrangement of 1-naphthyl acetate has been studied using steady state photolysis and laser flash photolysis. Kinetics of photo-Fries rearrangement of 1-napthyl acetate has been studied using steady-state, time-resolved chemically induced dynamic nuclear polarization (CIDNP) and flash photolysis methods.
Application
1-Naphthyl acetate may be used in a rapid staining method for identification of macrophages; counts by this method were confirmed by the more complex morphological criteria, by phagocytosis, and by the presence of Fc receptors. It may be employed as substrate to investigate the distribution of non-specific carboxylic esterases (EC 3.1.1) in the digestive tract of perch, Perm fliiviatilis L.
signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1
Clase de almacenamiento
11 - Combustible Solids
wgk
WGK 3
flash_point_f
235.4 °F
flash_point_c
113 °C
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Laser flash photolysis and CIDNP studies of 1-naphthyl acetate photo-Fries rearrangement.
Gritsan NP, et al.
The Journal of Physical Chemistry, 100(11), 4448-4458 (1996)
Magnetic isotope and external magnetic field effects upon the photo-Fries rearrangement of 1-naphthyl acetate.
Nakagaki R, et al.
The Journal of Physical Chemistry, 89(15), 3222-3226 (1985)
Non-specific carboxylic esterase activity in the digestive tract of the perch, Perca fluviatilis L.
Hirji KN and Courtney WAM.
Journal of Fish Biology, 22(1), 1-7 (1983)
Purification and kinetic characterisation of juvenile hormone esterase from Drosophila melanogaster.
P M Campbell et al.
Insect biochemistry and molecular biology, 28(7), 501-515 (1998-08-27)
Juvenile hormone esterase (JHE) from the prepupal stage of Drosophila melanogaster was purified about 429-fold to near homogeneity by selective precipitations, isoelectric focussing, anion exchange and gel filtration chromatography. The KM and Vmax of the purified enzyme for juvenile hormone
Zhuo Ma et al.
PloS one, 12(12), e0189343-e0189343 (2017-12-12)
Imidacloprid is a neonicotinoid insecticide that is effective against house fly, Musca domestica L., which is a major pest with the ability to develop resistance to insecticides. In the present study, we investigated the inheritance mode, the cross-resistance pattern and
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