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211737

Sigma-Aldrich

2-Amino-5-nitrobenzophenone

≥98%

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About This Item

Linear Formula:
H2NC6H3(NO2)C(O)C6H5
CAS Number:
1775-95-7
Molecular Weight:
242.23
EC Number:
217-207-9
MDL number:
MFCD00007364
UNSPSC Code:
12352100
PubChem Substance ID:
24852702
NACRES:
NA.22

Quality Level

100

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).

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
STBK6024
STBJ1034
STBG1830V
STBD9010V
STBD1892V

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Jochen Wiesner et al.
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
Koichi Saito et al.
Chemical & pharmaceutical bulletin, 69(3), 258-264 (2021-03-02)
The degradation behavior of eight benzodiazepines (BZPs): alprazolam, etizolam, diazepam, triazolam, nitrazepam (NZP), flunitrazepam (FNZ), bromazepam, and lorazepam, in artificial gastric juice was monitored by a LC/photodiode array detector (PDA) to estimate their pharmacokinetics in the stomach. For drugs that
T Inoue et al.
Journal of chromatography, 339(1), 163-169 (1985-04-12)
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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