ChemicalBook--->CAS DataBase List--->16091-26-2

16091-26-2

16091-26-2 Structure

16091-26-2 Structure
IdentificationMore
[Name]

3'-Aminobenzanilide
[CAS]

16091-26-2
[Synonyms]

3'-AMINOBENZANILIDE
3-AMINOBENZANILIDE
3-(AMINOPHENYL)BENZAMIDE
AKOS BB-8146
ART-CHEM-BB B025192
ASISCHEM B52474
M-BENZOYLAMINO ANILINE
N-(3-AMINOPHENYL)BENZAMIDE
3-Amino-N-phenylbenzamide
n-(3-aminophenyl)-benzamid
metaAmino Benzanilide
3-Benzoylaminoaniline
[EINECS(EC#)]

240-254-1
[Molecular Formula]

C13H12N2O
[MDL Number]

MFCD00071750
[Molecular Weight]

212.25
[MOL File]

16091-26-2.mol
Chemical PropertiesBack Directory
[Melting point ]

124-125°C
[Boiling point ]

308.3±25.0 °C(Predicted)
[density ]

1.244±0.06 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Inert atmosphere,Room temperature
[pka]

13.22±0.70(Predicted)
[Appearance]

Light yellow to yellow Solid
[CAS DataBase Reference]

16091-26-2(CAS DataBase Reference)
[NIST Chemistry Reference]

M-aminobenzanilide(16091-26-2)
[EPA Substance Registry System]

16091-26-2(EPA Substance)
Safety DataBack Directory
[Hazard Codes ]

Xi
[Risk Statements ]

R36/37/38:Irritating to eyes, respiratory system and skin .
[Safety Statements ]

S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection .
[TSCA ]

TSCA listed
[HazardClass ]

IRRITANT
Spectrum DetailBack Directory
[Spectrum Detail]

3'-Aminobenzanilide(16091-26-2)1HNMR
Well-known Reagent Company Product InformationBack Directory
[Sigma Aldrich]

16091-26-2(sigmaaldrich)
Hazard InformationBack Directory
[Synthesis]

N-(M-NITROPHENYL)BENZAMIDE

4771-08-8

3'-Aminobenzanilide

16091-26-2

The general procedure for the synthesis of m-aminobenzanilide from N-(3-nitrophenyl)benzamide was as follows: N-(3-nitrophenyl)benzamide (10a) was dissolved in ethanol (20 mL) and an aqueous solution of iron powder (2.5 g) and ammonium chloride (0.53 g, 10 mmol) was added. The reaction mixture was heated to reflux for 2 hours. After completion of the reaction, it was filtered while hot, the filtrate was collected and rotary evaporated to dryness. The resulting solid was dissolved in acetone, filtered to remove insoluble matter, the filtrate was collected and rotary evaporated to dryness to give m-aminobenzanilide (11a) in 89.8% yield.

[References]

[1] Synthesis (Germany), 2012, vol. 44, # 16, p. 2579 - 2586
[2] Synthetic Communications, 2000, vol. 30, # 20, p. 3639 - 3644
[3] Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry, 2000, vol. 39, # 9, p. 709 - 711
[4] Patent: CN106699755, 2017, A. Location in patent: Paragraph 0103; 0195; 0196
[5] Journal of Chemical Research, 2006, # 4, p. 223 - 224
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