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23218-93-1

23218-93-1 Structure

23218-93-1 Structure
IdentificationBack Directory
[Name]

3-AMINO-5-NITROBENZOIC ACID METHYL ESTER
[CAS]

23218-93-1
[Synonyms]

Methyl 3-amino-5-nitrobenzoate
3-Amino-5-nitro-methylbenzoate
3-amino-2-methyl-5-nitrobenzoate
3-AMINO-5-NITROBENZOIC ACID METHYL ESTER
5-Amino-3-nitrobenzoic acid methyl ester
Benzoic acid, 3-aMino-5-nitro-, Methyl ester
3-AMINO-5-NITRO-BENZOIC ACID METHYL ESTER >98%
3-(Methoxycarbonyl)-5-nitroaniline, 3-Amino-5-(methoxycarbonyl)nitrobenzene
[Molecular Formula]

C8H8N2O4
[MDL Number]

MFCD00461253
[MOL File]

23218-93-1.mol
[Molecular Weight]

196.16
Chemical PropertiesBack Directory
[Melting point ]

165-166°C (dec.)
[Boiling point ]

0°C
[density ]

1.386±0.06 g/cm3(Predicted)
[Fp ]

0°C
[storage temp. ]

Keep in dark place,Inert atmosphere,2-8°C
[form ]

powder
[pka]

1.34±0.10(Predicted)
[color ]

Yellow to red
[InChI]

InChI=1S/C8H8N2O4/c1-14-8(11)5-2-6(9)4-7(3-5)10(12)13/h2-4H,9H2,1H3
[InChIKey]

HZVBRLJDOZZHFL-UHFFFAOYSA-N
[SMILES]

C(OC)(=O)C1=CC([N+]([O-])=O)=CC(N)=C1
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P271-P261-P280
[Hazard Codes ]

Xi
[Risk Statements ]

36/37/38
[Safety Statements ]

26-36
[Hazard Note ]

Irritant
[HS Code ]

2922498590
Spectrum DetailBack Directory
[Spectrum Detail]

3-AMINO-5-NITROBENZOIC ACID METHYL ESTER(23218-93-1)1HNMR
Hazard InformationBack Directory
[Synthesis]

Methanol

67-56-1

3-Amino-5-nitrobenzoic acid

618-84-8

3-AMINO-5-NITROBENZOIC ACID METHYL ESTER

23218-93-1

General procedure for the synthesis of methyl 3-amino-5-nitrobenzoate from methanol and 3-amino-5-nitrobenzoic acid: The esterification reaction was carried out by passing dry hydrogen chloride gas into a solution of methanol (160 ml) containing 5-amino-3-nitrobenzoic acid (18.5 g, 0.10 mol). After the solution was saturated, the reaction mixture was stirred at room temperature overnight. Subsequently, the mixture was concentrated to a crystalline residue. The residue was dissolved in dichloromethane and washed with 5% sodium bicarbonate solution until the pH of the aqueous phase reached 7-8. The organic phase was separated, dried over magnesium sulfate and evaporated to remove the solvent. The product 18.6 g was obtained in 94% yield.1H NMR (CDCl3) data: δ 8.21 (t, 1H, J=1.5Hz), 4.19 (br s, 2H), 3.96 (s, 3H).

[References]

[1] Organic Letters, 2013, vol. 15, # 17, p. 4442 - 4445
[2] Patent: WO2007/29587, 2007, A1. Location in patent: Page/Page column 35
[3] Patent: WO2007/55580, 2007, A1. Location in patent: Page/Page column 16
[4] Patent: EP1953163, 2008, A1. Location in patent: Page/Page column 12
[5] Patent: WO2004/50619, 2004, A1. Location in patent: Page 16
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