Merck
CN

144517

Sigma-Aldrich

氨茴内酐

99%

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别名:
2,1-苯并异噁唑
经验公式(希尔记法):
C7H5NO
CAS号:
分子量:
119.12
EC 号:
MDL编号:
PubChem化学物质编号:
NACRES:
NA.22

质量水平

检测方案

99%

折射率

n20/D 1.584 (lit.)

bp

101-102 °C/15 mmHg (lit.)

密度

1.183 g/mL at 25 °C (lit.)

SMILES字符串

c1ccc2nocc2c1

InChI

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

InChI key

FZKCAHQKNJXICB-UHFFFAOYSA-N

一般描述

蒽醌在单脉冲激波管实验中发生热分解形成苯胺和环戊二烯腈 。研究了活性银胶体中蒽醌的表面增强拉曼光谱

象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

Acute Tox. 4 Oral

储存分类代码

10 - Combustible liquids

WGK

WGK 3

闪点(°F)

201.2 °F - closed cup

闪点(°C)

94 °C - closed cup

法规信息

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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
Further exploration of stages in carcinogenesis.
V Armuth et al.
Carcinogenesis; a comprehensive survey, 7, 41-42 (1982-01-01)
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
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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