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Merck

214671

Sigma-Aldrich

3-乙酰基香豆素

96%

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About This Item

经验公式(希尔记法):
C11H8O3
CAS号:
分子量:
188.18
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

化驗

96%

形狀

solid

mp

119-122 °C (lit.)

SMILES 字串

CC(=O)C1=Cc2ccccc2OC1=O

InChI

1S/C11H8O3/c1-7(12)9-6-8-4-2-3-5-10(8)14-11(9)13/h2-6H,1H3

InChI 密鑰

CSPIFKKOBWYOEX-UHFFFAOYSA-N

一般說明

已经报道了 3-乙酰香豆素的 FTIR 和 FT-拉曼光谱。3-乙酰香豆素在哌啶存在下与氯仿中的芳基醛缩合,生成含有 4-芳基丁-3-烯-2-酮成分的香豆素衍生物

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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Abdullah Sulaiman Al-Ayed
Molecules (Basel, Switzerland), 16(12), 10292-10302 (2011-12-14)
A series of new coumarin derivatives 4 containing a 4-arylbut-3-en-2-one moiety were synthesized by condensation of 3-acetylcoumarin 1 with aryl aldehydes 2 in chloroform in the presence of piperidine. The interactions of 3-formyl-4-chlorocoumarin (3) with nitrogen-containg nucleophiles leading to the
X L Huang et al.
Yao xue xue bao = Acta pharmaceutica Sinica, 31(6), 431-436 (1996-01-01)
Twenty-five 3-acetylcoumarin derivatives were synthesized among which twenty-two were not reported before. Antimutagenic activity screen in vitro has shown that some of these compounds have various activities. The structure and activity relationship for 5-, 7-, 8-substituents has been studied. Pharmacological
Wafaa S Hamama et al.
Archiv der Pharmazie, 344(11), 710-718 (2011-09-29)
3-Acetylcoumarin (1) was utilized as a key intermediate for the synthesis of 2-aminothiazole derivative 3 via bromination of 1 to afford acetylbromide 2 followed by treatment with thiourea or via Biginelli reaction of 1. Treatment of 3 with 5-chloro-3-methyl-1-phenyl-1H-pyrazole-4-carbaldehyde, 2-methyl-4H-benzo[d][1,3]oxazin-4-one
Jhi Biau Foo et al.
Biometals : an international journal on the role of metal ions in biology, biochemistry, and medicine, 31(4), 505-515 (2018-04-07)
Copper complexes have been widely studied for the anti-tumour application as cancer cells are reported to take up greater amounts of copper than normal cells. Preliminary study revealed that the newly synthesised copper complex [Cu(SBCM)2] displayed marked anti-proliferative towards triple-negative
V Arjunan et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 109, 79-89 (2013-03-19)
3-Acetylcoumarin (3AC) was synthesised by a Knoevenagel reaction. Conformational analysis using the B3LYP method was also carried out to determine the most stable conformation of the compound. FTIR and FT-Raman spectra of 3AC have been recorded in the range 4000-400

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