211737
2-Amino-5-nitrobenzophenone
≥98%
Přihlásitk zobrazení cen stanovených pro organizaci a smluvních cen
About This Item
Lineární vzorec:
H2NC6H3(NO2)C(O)C6H5
Číslo CAS:
Molekulová hmotnost:
242.23
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Doporučené produkty
![BICYCLO[2.2.1]HEPT-5-ENE-2-CARBONITRILE AldrichCPR](/deepweb/assets/sigmaaldrich/product/structures/423/632/9f9c4d06-10c1-4935-ac11-4f0e71373dd4/640/9f9c4d06-10c1-4935-ac11-4f0e71373dd4.png)
Quality Level
assay
≥98%
form
powder
mp
166-168 °C (lit.)
functional group
ketone
nitro
phenyl
SMILES string
Nc1ccc(cc1C(=O)c2ccccc2)[N+]([O-])=O
InChI
1S/C13H10N2O3/c14-12-7-6-10(15(17)18)8-11(12)13(16)9-4-2-1-3-5-9/h1-8H,14H2
InChI key
PZPZDEIASIKHPY-UHFFFAOYSA-N
General description
FT-IR and Raman spectra of 2-amino-5-nitrobenzophenone (ANBP) has been reported.
Application
2-Amino-5-nitrobenzophenone was used in the synthesis of [5-(4-nitrophenyl)-2-furyl]acrylic acid substituted benzophenone (anti-malarial agent).
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Bioorganic & medicinal chemistry letters, 13(3), 361-363 (2003-02-05)
We have developed the [5-(4-nitrophenyl)-2-furyl]acrylic acid substituted benzophenone 4g as a novel lead for anti-malarial agents. Here, we demonstrated that the acyl residue at the 2-amino group of the benzophenone core structure has to be a phenylacetic acid substructure substituted
V Balachandran et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 118, 835-846 (2013-10-25)
The FT-IR and Raman spectra of 2-amino-5-nitrobenzophenone (ANBP) molecule have been recorded using Brucker IFS 66 V spectrometer in the range of 4000-100 cm(-1). The molecular geometry and vibrational frequencies in the ground state are calculated using the Hartree-Fock (HF)
P J Cox et al.
International journal of pharmaceutics, 194(2), 147-153 (2000-02-29)
The role of single crystal diffraction in the quantitative determination of polymorphism is demonstrated by the examination of three compounds. Two polymorphs were found for each of the compounds bis(2-nitrophenyl) trisulphide (1), 2-amino-5-nitrobenzophenone (2) and bis(2-nitrophenyl) sulphide (3). Only in
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A method for the direct quantitative densitometry of nitrazepam and its main metabolites (7-aminonitrazepam, 7-acetamidonitrazepam and 2-amino-5-nitrobenzophenone) in urine was developed. The unchanged drug and its metabolites were extracted with benzene-dichloromethane (4:1), subjected to thin-layer chromatography, and determined by direct
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