ChemicalBook--->CAS DataBase List--->3095-48-5

3095-48-5

3095-48-5 Structure

3095-48-5 Structure
IdentificationBack Directory
[Name]

4-AMINO-3,5-DIMETHYL-BENZOIC ACID METHYL ESTER
[CAS]

3095-48-5
[Synonyms]

Methyl 4-aMino-3,5-diMethylbenzoate
4-AMINO-3,5-DIMETHYL-BENZOIC ACID METHYL ESTER
Benzoic acid, 4-aMino-3,5-diMethyl-, Methyl ester
[Molecular Formula]

C10H13NO2
[MDL Number]

MFCD09833906
[MOL File]

3095-48-5.mol
[Molecular Weight]

179.22
Chemical PropertiesBack Directory
[Melting point ]

106-107℃
[Boiling point ]

331.3±37.0 °C(Predicted)
[density ]

1.105±0.06 g/cm3(Predicted)
[storage temp. ]

2-8°C(protect from light)
[pka]

2.17±0.10(Predicted)
[Appearance]

Light yellow to brown Solid
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[HS Code ]

2922498590
Spectrum DetailBack Directory
[Spectrum Detail]

4-AMINO-3,5-DIMETHYL-BENZOIC ACID METHYL ESTER(3095-48-5)1HNMR
Hazard InformationBack Directory
[Synthesis]

Methyl 3,5-dimethyl-4-nitrobenzoate

3277-04-1

4-AMINO-3,5-DIMETHYL-BENZOIC ACID METHYL ESTER

3095-48-5

Scheme 5, Step B. To a solution of methyl 3,5-dimethyl-4-nitrobenzoate (10.0 g, 0.0478 mol) in methanol (100 mL) at 0°C was sequentially added iron powder (15.7 g, 0.2869 mol) and 37% hydrochloric acid (1.72 g, 0.0478 mol). The reaction mixture was heated to 80 °C and kept for 16 hours. After completion of the reaction, the mixture was cooled to room temperature, filtered through a Celite TM bed and the filter cake was washed with methanol. The filtrate was concentrated to dryness to afford methyl 4-amino-3,5-dimethylbenzoate as an unpurified solid (7.8 g, 99% yield). Mass spectrum (m/z): 180.2 (M + 1).

[References]

[1] Patent: US6342610, 2002, B2. Location in patent: Page column 125
[2] Patent: WO2014/4230, 2014, A1. Location in patent: Sheet 18; 19
[3] Patent: WO2015/94912, 2015, A1. Location in patent: Page/Page column 10
[4] Bioorganic and Medicinal Chemistry Letters, 2016, vol. 26, # 1, p. 105 - 109
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