255254
3-氨基二苯甲酮
97%
别名:
3-氨基苯并苯酮
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关于此项目
线性分子式:
H2NC6H4C(O)C6H5
化学文摘社编号:
分子量:
197.23
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
220-614-4
MDL number:
Assay:
97%
InChI key
FUADXEJBHCKVBN-UHFFFAOYSA-N
InChI
1S/C13H11NO/c14-12-8-4-7-11(9-12)13(15)10-5-2-1-3-6-10/h1-9H,14H2
SMILES string
Nc1cccc(c1)C(=O)c2ccccc2
assay
97%
mp
81-84 °C (lit.)
functional group
ketone, phenyl
Quality Level
General description
3-Aminobenzophenone forms cyclodextrin (α and β) based nanostructures through the supramolecular self assembly.
Application
3-Aminobenzophenone has been used in the synthesis of racemic benzophenone ureas, chiral photoaffinity labeling probes.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
法规信息
新产品
此项目有
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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