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5-Nitro-2-aminobenzophenone

2-Amino-5-nitrobenzophenone

CAS: 1775-95-7

Molecular Formula: C13H10N2O3

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  5. 5-Nitro-2-aminobenzophenone

5-Nitro-2-aminobenzophenone - Names and Identifiers

Name 2-Amino-5-nitrobenzophenone
Synonyms BRN 0748830
2-Benzoyl-4-nitroaniline
2-Amino-5-nitrodiphenylone
2-Amino-5-nitrobenzophenone
5-Nitro-2-aminobenzophenone
Benzophenone, 2-amino-5-nitro-
2-Amino-5-nitrodiphenylmethone
(2-Amino-5-nitrophenyl)phenylmethanone
(2-amino-5-nitrophenyl)phenyl-methanon
Methanone,(2-amino-5-nitrophenyl)phenyl-
Methanone, (2-amino-5-nitrophenyl)phenyl-
4-14-00-00246 (Beilstein Handbook Reference)
CAS 1775-95-7
EINECS 217-207-9
InChI InChI=1/C13H10N2O3/c14-12-7-6-10(15(17)18)8-11(12)13(16)9-4-2-1-3-5-9/h1-8H,14H2

5-Nitro-2-aminobenzophenone - Physico-chemical Properties

Molecular FormulaC13H10N2O3
Molar Mass242.23
Density1.2480 (rough estimate)
Melting Point166-168 °C (lit.)
Boling Point385.05°C (rough estimate)
Flash Point242.9°C
Water Solubility3 mg/L (20 C)
Solubility Chloroform (Slightly), DMSO (Slightly), Methanol (Slightly, Heated)
Vapor Presure2.65E-09mmHg at 25°C
AppearanceYellow crystalline powder
ColorBeige
pKa-2.26±0.36(Predicted)
Storage ConditionKeep in dark place,Inert atmosphere,Room temperature
Refractive Index1.5300 (estimate)
MDLMFCD00007364
Physical and Chemical PropertiesYellow crystalline powder
UseUsed as an intermediate

5-Nitro-2-aminobenzophenone - Risk and Safety

Risk CodesR36/37/38 - Irritating to eyes, respiratory system and skin.
R20/21/22 - Harmful by inhalation, in contact with skin and if swallowed.
Safety DescriptionS26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S37/39 - Wear suitable gloves and eye/face protection
S36 - Wear suitable protective clothing.
WGK Germany3
RTECSPC4935000
HS Code29223990

5-Nitro-2-aminobenzophenone - Upstream Downstream Industry

Raw Materials4-Chlorobenzoic acid

5-Nitro-2-aminobenzophenone - Introduction

Soluble in ethanol and acetic acid, solubility: 3 MG/L water (20 C),0.21G/100 ML methanol, 0.21G/100 ML ethanol, 0.15G/100 ML isopropanol, 17G/100 ML N,N-DMF,3G/100 ML acetone, 1.5G/100 ML chloroform.
Last Update:2022-10-16 17:14:29

5-Nitro-2-aminobenzophenone - Reference Information

NIST chemical information Information provided by: webbook.nist.gov (external link)
use as a pharmaceutical intermediate.
Used as an intermediate
Production method It is obtained by condensation of p-nitroaniline and benzoyl chloride. Add p-nitroaniline, benzoyl chloride and zinc chloride into the reaction tank and stir, and heat to melt all the materials. Raise the temperature to 140 ℃ and keep the temperature for 30min. Continue to raise the temperature to about 200 ℃, hold the temperature for 2 hours, cool to 115-120 ℃, stir and hydrolyze for 15 hours. Add 2.5 times dilute hydrochloric acid, cool to 35 ℃, and filter. The filter cake is washed with dilute hydrochloric acid and filtered dry. Add 4 times the amount of water to stir into paste, add alkali to pH 11, soak for 2-3h (add alkali to pH 11 during soaking). Filter and wash the filter cake with water to make the pH 6-7. Filter and dry to obtain crude benzophenone. Add appropriate amount of activated carbon and 10 times the amount of ethanol, and heat and reflux for 4 hours. Filter while hot. The filtrate is cooled and crystallized. Filter, wash the cake with cold ethanol, filter dry, dry to get. The yield was 25%.
Last Update:2024-04-09 02:00:07
5-Nitro-2-aminobenzophenone
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View History
5-Nitro-2-aminobenzophenone
1823320-19-9
Raw Materials for 5-Nitro-2-aminobenzophenone
4-Chlorobenzoic acid
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