ChemicalBook--->CAS DataBase List--->6083-47-2

6083-47-2

6083-47-2 Structure

6083-47-2 Structure
IdentificationBack Directory
[Name]

4-(Dimethylamino)benzamide
[CAS]

6083-47-2
[Synonyms]

4-(Dimethylamino)benzamide
Benzamide, 4-(dimethylamino)-
[Molecular Formula]

C9H12N2O
[MDL Number]

MFCD01216782
[MOL File]

6083-47-2.mol
[Molecular Weight]

164.2
Chemical PropertiesBack Directory
[Melting point ]

203.5 °C
[Boiling point ]

325.5±25.0 °C(Predicted)
[density ]

1.123±0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[pka]

16.89±0.50(Predicted)
[Appearance]

White to off-white Solid
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H319-H335-H302-H315
[Precautionary statements ]

P264-P280-P305+P351+P338-P337+P313P-P264-P270-P301+P312-P330-P501-P264-P280-P302+P352-P321-P332+P313-P362
[HS Code ]

2924297099
Spectrum DetailBack Directory
[Spectrum Detail]

4-(Dimethylamino)benzamide(6083-47-2)1HNMR
Hazard InformationBack Directory
[Synthesis]

4-Dimethylaminobenzaldehyde

100-10-7

4-(Dimethylamino)benzamide

6083-47-2

General procedure for the synthesis of 4-(dimethylamino)benzamide from p-dimethylaminobenzaldehyde: In a 10 mL pressurized vial, Sc(OTf)3 (10 mol%, 49 mg), p-dimethylaminobenzaldehyde (1 mmol), NH2OH-HCl (1 mmol, 69 mg), and Na2CO3 (1 mmol) were added, followed by H2O (1 mL). The vials were sealed using snap-on lids and placed in a single-mode CEM Discover Bench Mate microwave reactor and irradiated at 300 W power and 135 °C for 15-35 min. The progress of the reaction was monitored by TLC during the reaction. Upon completion of the reaction, the mixture was cooled to room temperature and extracted with EtOAc (3 × 10 mL). The organic phases were combined, dried with Na2SO4, filtered and concentrated under reduced pressure. The residue was purified by silica gel column chromatography using EtOAc/hexane (3:7) as eluent and the final product was characterized by physical properties and spectral data.

[References]

[1] Journal of Materials Chemistry, 2012, vol. 22, # 35, p. 18115 - 18118
[2] European Journal of Organic Chemistry, 2011, # 12, p. 2226 - 2229
[3] Tetrahedron Letters, 2011, vol. 52, # 44, p. 5851 - 5854
[4] Catalysis Communications, 2017, vol. 91, p. 38 - 42
[5] Organic Letters, 2016, vol. 18, # 22, p. 5788 - 5791
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