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144517

Sigma-Aldrich

Anthranil

99%

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Synonym(s):
2,1-Benzisoxazole
Empirical Formula (Hill Notation):
C7H5NO
CAS Number:
Molecular Weight:
119.12
EC Number:
MDL number:
PubChem Substance ID:
NACRES:
NA.22

Quality Level

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.)

SMILES string

c1ccc2nocc2c1

InChI

1S/C7H5NO/c1-2-4-7-6(3-1)5-9-8-7/h1-5H

InChI key

FZKCAHQKNJXICB-UHFFFAOYSA-N

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This Item
10680PHR1677A89855
Anthranil 99%

144517

Anthranil

Anthranilic acid puriss. p.a., ≥99.5% (T)

10680

Anthranilic acid

Anthralin (Dithranol) Pharmaceutical Secondary Standard; Certified Reference Material

PHR1677

Anthralin (Dithranol)

Anthranilic acid reagent grade, ≥98%

A89855

Anthranilic acid

refractive index

n20/D 1.584 (lit.)

refractive index

-

refractive index

-

refractive index

-

bp

101-102 °C/15 mmHg (lit.)

bp

-

bp

-

bp

-

density

1.183 g/mL at 25 °C (lit.)

density

-

density

-

density

-

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.

pictograms

Exclamation mark

signalword

Warning

hcodes

Hazard Classifications

Acute Tox. 4 Oral

Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

flash_point_f

201.2 °F - closed cup

flash_point_c

94 °C - closed cup


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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
A possible in vivo skin model for tumour promoter assays.
V Armuth et al.
Cancer letters, 15(3), 343-346 (1982-03-01)
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)

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