ChemicalBook--->CAS DataBase List--->63435-16-5

63435-16-5

63435-16-5 Structure

63435-16-5 Structure
IdentificationMore
[Name]

Methyl 4-amino-3-hydroxybenzoate
[CAS]

63435-16-5
[Synonyms]

3-HYDROXY-4-AMINOBENZOIC ACID ETHYL ESTER
4-AMINO-3-HYDROXYBENZOIC ACID ETHYL ESTER
METHYL-3-HYDROXY-4-AMINOBENZOATE
METHYL 4-AMINO-3-HYDROXYBENZENECARBOXYLATE
METHYL 4-AMINO-3-HYDROXYBENZOATE
4-Amino-3-hydroxybenzoic acid methyl ester
3-HYDROXY-4-AMINOBENZOIC ACID ETHYL ESTER 97%
3-Hydroxy-4-aminobenzoic acid methyl ester
[Molecular Formula]

C8H9NO3
[MDL Number]

MFCD01320538
[Molecular Weight]

167.16
[MOL File]

63435-16-5.mol
Chemical PropertiesBack Directory
[Melting point ]

120-122°C
[Boiling point ]

364.5±27.0 °C(Predicted)
[density ]

1.305±0.06 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Sealed in dry,2-8°C
[form ]

solid
[pka]

8.94±0.10(Predicted)
[color ]

Brown
[BRN ]

608716
[InChI]

InChI=1S/C8H9NO3/c1-12-8(11)5-2-3-6(9)7(10)4-5/h2-4,10H,9H2,1H3
[InChIKey]

OCZXDVNSNDITBS-UHFFFAOYSA-N
[SMILES]

C(OC)(=O)C1=CC=C(N)C(O)=C1
[CAS DataBase Reference]

63435-16-5(CAS DataBase Reference)
[NIST Chemistry Reference]

Methyl 4-amino-3-hydroxybenzoate(63435-16-5)
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:Wear suitable protective clothing .
[WGK Germany ]

3
[Hazard Note ]

Irritant
[HazardClass ]

IRRITANT
[HS Code ]

2922500090
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Acute Tox. 4 Oral
Hazard InformationBack Directory
[Uses]

Methyl 4-amino-3-hydroxybenzoate is used as an important raw material and intermediate used in Organic Synthesis, Pharmaceuticals, Agrochemicals and Dyestuff.
[Synthesis]

Methanol

67-56-1

4-Amino-3-hydroxybenzoic acid

2374-03-0

Methyl 4-amino-3-hydroxybenzoate

63435-16-5

1. 4-Amino-3-hydroxybenzoic acid (5.0 g, 32.6 mmol) was slowly added dropwise to a mixture of 1.25 M HCl solution (100 mL) and methanol (100 mL) at 0 °C. 2. After the dropwise addition, the reaction mixture was gradually warmed up to room temperature with continuous stirring overnight. 3. The reaction process was monitored by HPLC and it was found that there was still raw material left, so the mixture was continued to be stirred at room temperature for 48 hours. 4. After completion of the reaction, the solvent was removed by distillation under reduced pressure. 5. 5. The residue was treated with saturated aqueous sodium bicarbonate solution, followed by extraction of the aqueous phase with ethyl acetate (2×). 6. The organic extracts were combined, washed with brine, dried over anhydrous sodium sulfate, filtered and concentrated to dryness to afford the title compound methyl 4-amino-3-hydroxybenzoate (5.37 g, 97% yield) as a crystalline solid. 7. The molecular weight of the product was confirmed to be 168 (M+1)+ by low resolution mass spectrometry (LRMS) analysis.

[References]

[1] Patent: WO2013/68552, 2013, A1. Location in patent: Page/Page column 70
[2] Patent: WO2013/68554, 2013, A1. Location in patent: Page/Page column 80
[3] Bioorganic and Medicinal Chemistry Letters, 2001, vol. 11, # 10, p. 1257 - 1260
[4] Patent: EP1382607, 2004, A2. Location in patent: Page 43
[5] Organic and Biomolecular Chemistry, 2016, vol. 14, # 15, p. 3782 - 3786
Spectrum DetailBack Directory
[Spectrum Detail]

Methyl 4-amino-3-hydroxybenzoate(63435-16-5)1HNMR
Well-known Reagent Company Product InformationBack Directory
[Alfa Aesar]

Methyl 4-amino-3-hydroxybenzoate, 98%(63435-16-5)
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