144517
Anthranil
99%
Synonym(s):
2,1-Benzisoxazole
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About This Item
Empirical Formula (Hill Notation):
C7H5NO
CAS Number:
Molecular Weight:
119.12
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
205-980-5
MDL number:
Assay:
99%
InChI key
FZKCAHQKNJXICB-UHFFFAOYSA-N
InChI
1S/C7H5NO/c1-2-4-7-6(3-1)5-9-8-7/h1-5H
SMILES string
c1ccc2nocc2c1
assay
99%
refractive index
n20/D 1.584 (lit.)
bp
101-102 °C/15 mmHg (lit.)
density
1.183 g/mL at 25 °C (lit.)
Quality Level
Related Categories
General description
Anthranil undergoes thermal decomposition during single pulse shock-tube experiments to form aniline and cyclopentadiene carbonitrile. Surface-enhanced Raman spectrum of anthranil in activated silver colloid has been studied.
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Marna Pippel et al.
Bioorganic & medicinal chemistry letters, 19(22), 6373-6375 (2009-10-09)
A series of CCK2R-selective anthranilic amides is shown to derive CCK1R affinity via selective substitution of the amide side chain. Thus, extending the length of the original benzamide side chain by a single methylene unit imparts CCK1R affinity to the
Further exploration of stages in carcinogenesis.
V Armuth et al.
Carcinogenesis; a comprehensive survey, 7, 41-42 (1982-01-01)
Assa Lifshitz et al.
The journal of physical chemistry. A, 110(27), 8248-8258 (2006-07-11)
The thermal decomposition of anthranil diluted in argon was studied behind reflected shock waves in a 2 in. i.d. pressurized driver single-pulse shock tube over the temperature range 825-1000 K and overall densities of approximately 3 x 10(-5) mol/cm(3). Two
E V Kudryashova et al.
Biochimica et biophysica acta, 1550(2), 129-143 (2002-01-05)
Structure and dynamic properties of free poly(methacrylic acid) (PMA) and PMA complexed with alpha-chymotrypsin (CT) were studied using the time resolved fluorescence anisotropy technique. We have found that the interaction of PMA with CT induces the formation of a quasi-regular
Marna Pippel et al.
Bioorganic & medicinal chemistry letters, 19(22), 6376-6378 (2009-10-10)
In the previous article we demonstrated how certain CCK2R-selective anthranilic amides could be structurally modified to afford high-affinity, selective CCK1R activity. We now describe our efforts at modulating and optimizing the CCK1R and CCK2R affinities aimed at producing compounds with
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