推薦產品
化驗
97%
形狀
solid
mp
135-139 °C (lit.)
官能基
ester
SMILES 字串
NC1=Cc2ccccc2OC1=O
InChI
1S/C9H7NO2/c10-7-5-6-3-1-2-4-8(6)12-9(7)11/h1-5H,10H2
InChI 密鑰
QWZHDKGQKYEBKK-UHFFFAOYSA-N
應用
3-氨基香豆素可用于以下研究：
- 作为合成 Cr (III)、Ni (II) 和 Cu (II) 配合物的配体。
- 作为合成 1,2,3,4-四氢吡啶类 [2,3- c ] 香豆素的起始试剂。
- 通过优化的 Buchwald-Hartwig 胺化反应合成新的 3-（杂芳基）氨基香豆素衍生物。
訊號詞
Warning
危險聲明
危險分類
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
標靶器官
Respiratory system
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
dust mask type N95 (US), Eyeshields, Gloves
客戶也查看了
Synthesis of biologically potent new 3-(heteroaryl) aminocoumarin derivatives via Buchwald-Hartwig C-N coupling.
Das AR, et al.
Tetrahedron Letters, 51(7), 1099-1102 (2010)
Fluorescence spectra of 3-aminocoumarin and its acid-base behaviour in the excited singlet state.
Rao RVS, et al.
Journal of Photochemistry, 34(1), 55-61 (1986)
Abdul Amir H Kadhum et al.
Molecules (Basel, Switzerland), 16(8), 6969-6984 (2011-08-17)
3-Aminocoumarin (L) has been synthesized and used as a ligand for the formation of Cr(III), Ni(II), and Cu(II) complexes. The chemical structures were characterized using different spectroscopic methods. The elemental analyses revealed that the complexes where M=Ni(II) and Cu(II) have
Iu A Vladimirov et al.
Biulleten' eksperimental'noi biologii i meditsiny, 112(10), 358-360 (1991-10-01)
The antioxidant capacity of 3-aminocoumarin, 3-oxycoumarin, 3-acetylaminocoumarin, and 3-coumarin carbonic acid has been investigated with chemiluminescence measurement and by the accumulation of TBA-active products. All coumarins were found to be antioxidants, with 3-oxy-, 3-amino- and 3-acetylamino coumarins being capable of
Hydrolysis-free synthesis of 3-aminocoumarins.
Kudale AA, et al.
Tetrahedron Letters, 48(29), 5077-5080 (2007)
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