ChemicalBook--->CAS DataBase List--->66315-16-0

66315-16-0

66315-16-0 Structure

66315-16-0 Structure
IdentificationBack Directory
[Name]

Methyl 3-amino-4-(methylamino)benzenecarboxylate
[CAS]

66315-16-0
[Synonyms]

Methyl 3-aMino-4-(MethylaMino)benzoate
3-Amino-4-(methylamino)benzoesaeure-methylester
3-Amino-4-methylamino-benzoic acid methyl ester
Methyl 3-amino-4-(methylamino)benzenecarboxylate
Benzoic acid, 3-amino-4-(methylamino)-, methyl ester
[Molecular Formula]

C9H12N2O2
[MDL Number]

MFCD12922710
[MOL File]

66315-16-0.mol
[Molecular Weight]

180.2
Chemical PropertiesBack Directory
[Melting point ]

103-105°
[Boiling point ]

346.5±32.0 °C(Predicted)
[density ]

1.208±0.06 g/cm3(Predicted)
[storage temp. ]

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

5.40±0.11(Predicted)
[Appearance]

Gray to dark gray Solid
Safety DataBack Directory
[Symbol(GHS) ]


GHS05,GHS02
[Signal word ]

Danger
[Hazard statements ]

H314-H228
[Precautionary statements ]

P501-P260-P240-P210-P241-P264-P280-P370+P378-P303+P361+P353-P301+P330+P331-P363-P304+P340+P310-P305+P351+P338+P310-P405
[Hazard Codes ]

Xi
[Risk Statements ]

43
[Safety Statements ]

36/37
[HazardClass ]

IRRITANT
[HS Code ]

2922498590
Spectrum DetailBack Directory
[Spectrum Detail]

Methyl 3-amino-4-(methylamino)benzenecarboxylate(66315-16-0)1HNMR
Hazard InformationBack Directory
[Synthesis]

2-(methylamino)-5-(methoxycarbonyl)-3-nitrobenzene

36242-50-9

Methyl 3-amino-4-(methylamino)benzenecarboxylate

66315-16-0

General procedure for the synthesis of methyl 3-amino-4-(methylamino)benzoate from methyl 4-(methylamino)-3-nitrobenzoate: Methyl 4-(methylamino)-3-nitrobenzoate (540 mg, 2.5 mmol) was dissolved in a solvent mixture of ethyl acetate and methanol (2:1 v/v/v, 20 mL). A 10% palladium-carbon catalyst (5 mol%) was added to the solution under nitrogen protection. The reaction mixture was placed in a hydrogen atmosphere and the reaction was stirred for 4 hours. Upon completion of the reaction, the catalyst was removed by diatomaceous earth filtration. The filtrate was concentrated under reduced pressure to afford the target product methyl 3-amino-4-(methylamino)benzoate. The product was characterized by LC-MS with molecular ion peak [M + 1] = 181.1. yield: 441 mg (100% yield).

[References]

[1] Patent: EP1502916, 2005, A1. Location in patent: Page 440
[2] Patent: WO2007/69053, 2007, A1. Location in patent: Page/Page column 34
[3] Patent: WO2008/65508, 2008, A1. Location in patent: Page/Page column 32-33; 38-40
[4] Patent: WO2017/147102, 2017, A1. Location in patent: Paragraph 00126-00127
[5] Patent: WO2017/100594, 2017, A1. Location in patent: Paragraph 00132
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