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Merck

255254

Sigma-Aldrich

3-氨基二苯甲酮

97%

别名:

3-氨基苯并苯酮

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About This Item

线性分子式:
H2NC6H4C(O)C6H5
CAS号:
分子量:
197.23
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

81-84 °C (lit.)

SMILES 字串

Nc1cccc(c1)C(=O)c2ccccc2

InChI

1S/C13H11NO/c14-12-8-4-7-11(9-12)13(15)10-5-2-1-3-6-10/h1-9H,14H2

InChI 密鑰

FUADXEJBHCKVBN-UHFFFAOYSA-N

一般說明

3-Aminobenzophenone forms cyclodextrin (α and β) based nanostructures through the supramolecular self assembly.

應用

3-Aminobenzophenone has been used in the synthesis of racemic benzophenone ureas, chiral photoaffinity labeling probes.

象形圖

Exclamation mark

訊號詞

Warning

危險聲明

危險分類

Eye Irrit. 2 - Skin Irrit. 2

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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N Rajendiran et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 127, 52-60 (2014-03-19)
Cyclodextrin (α and β) based nanostructures formed with 2-aminobenzophenone, 3-aminobenzophenone through the supramolecular self assembly are studied by absorption, fluorescence, time-resolved fluorescence, SEM, TEM, FT-IR, DSC, PXRD and (1)H NMR. The unequal layer by layer nanosheets and nanoribbons are formed
Elizabeth M Hadac et al.
Journal of medicinal chemistry, 49(3), 850-863 (2006-02-03)
An understanding of the molecular basis of drug action provides opportunities for refinement of drug properties and for development of more potent and selective molecules that act at the same biological target. In this work, we have identified the active

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