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Merck

I2606

Sigma-Aldrich

3-吲唑啉酮

97%

别名:

3-羟基-1H-吲唑

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About This Item

经验公式(希尔记法):
C7H6N2O
CAS号:
分子量:
134.14
Beilstein:
3733
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

化驗

97%

mp

250-252 °C (lit.)

SMILES 字串

O=C1NNc2ccccc12

InChI

1S/C7H6N2O/c10-7-5-3-1-2-4-6(5)8-9-7/h1-4H,(H2,8,9,10)

InChI 密鑰

SWEICGMKXPNXNU-UHFFFAOYSA-N

基因資訊

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儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

Eyeshields, Gloves, type N95 (US)


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Pedro González-Naranjo et al.
Bioorganic & medicinal chemistry, 28(19), 115672-115672 (2020-09-12)
Synthesis and pharmacological evaluation of a new series of cannabinoid receptor antagonists of indazole ether derivatives have been performed. Pharmacological evaluation includes radioligand binding assays with [3H]-CP55940 for CB1 and CB2 receptors and functional activity for cannabinoid receptors on isolated
S D Wyrick et al.
Journal of medicinal chemistry, 27(6), 768-772 (1984-06-01)
The apparent benefit of limiting serum cholesterol and triglyceride levels either by dietary restriction or drug therapy has prompted work in our laboratories toward development of a suitable antihyperlipidemic agent. We have demonstrated the antihyperlipidemic activity of a series of
G E Demas et al.
Molecular medicine (Cambridge, Mass.), 3(9), 610-616 (1997-11-05)
Mice with targeted disruption of the gene for the neuronal isoform of nitric oxide synthase (nNOS) display exaggerated aggression. Behavioral studies of mice with targeted gene deletions suffer from the criticism that the gene product is missing not only during

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