ChemicalBook--->CAS DataBase List--->27883-60-9

27883-60-9

27883-60-9 Structure

27883-60-9 Structure
IdentificationBack Directory
[Name]

4-HYDROXY-5-METHOXY-2-NITRO-BENZOIC ACID METHYL ESTER
[CAS]

27883-60-9
[Synonyms]

4-hydroxy-5-methoxy-2-nitrobenzoic acid
Methyl 4-hydroxy-5-Methoxy-2-nitrobenzoate
4-HYDROXY-5-METHOXY-2-NITRO-BENZOIC ACID METHYL ESTER
Benzoic acid, 4-hydroxy-5-methoxy-2-nitro-, methyl ester
[Molecular Formula]

C9H9NO6
[MDL Number]

MFCD09833001
[MOL File]

27883-60-9.mol
[Molecular Weight]

227.17
Chemical PropertiesBack Directory
[Boiling point ]

389.2±42.0 °C(Predicted)
[density ]

1.405±0.06 g/cm3(Predicted)
[storage temp. ]

Inert atmosphere,Room Temperature
[pka]

6.63±0.24(Predicted)
[Appearance]

Brown to reddish brown Solid
[InChI]

InChI=1S/C9H9NO6/c1-15-8-3-5(9(12)16-2)6(10(13)14)4-7(8)11/h3-4,11H,1-2H3
[InChIKey]

SKKNLIAUOSEGNQ-UHFFFAOYSA-N
[SMILES]

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

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P271-P261
[HazardClass ]

IRRITANT
[HS Code ]

2916310090
Spectrum DetailBack Directory
[Spectrum Detail]

4-HYDROXY-5-METHOXY-2-NITRO-BENZOIC ACID METHYL ESTER(27883-60-9)1HNMR
Hazard InformationBack Directory
[Synthesis]

Methyl 4-(benzyloxy)-5-methoxy-2-nitrobenzoate

61032-41-5

4-HYDROXY-5-METHOXY-2-NITRO-BENZOIC ACID METHYL ESTER

27883-60-9

General procedure for the synthesis of methyl 4-hydroxy-5-methoxy-2-nitrobenzoate from methyl 4-benzyloxy-5-methoxy-2-nitrobenzoate: Methyl 2-nitro-4-benzyloxy-5-methoxybenzoate (4.1 mmol, 1.3 g) was dissolved in trifluoroacetic acid (8 mL), and the reaction was carried out at reflux for 1 hour. Upon completion of the reaction, trifluoroacetic acid was removed by decantation and the reaction mixture was extracted with water and ethyl acetate. The organic phases were combined, concentrated and purified by column chromatography to give 0.796 g methyl 2-nitro-4-hydroxy-5-methoxybenzoate in 86% yield.

[References]

[1] Patent: CN105884699, 2016, A. Location in patent: Paragraph 0064; 0065
[2] Patent: WO2016/148674, 2016, A1. Location in patent: Page/Page column 114
[3] Bioorganic and medicinal chemistry, 2004, vol. 12, # 16, p. 4337 - 4350
[4] Journal of Medicinal Chemistry, 2018, vol. 61, # 15, p. 6518 - 6545
[5] Bioorganic and Medicinal Chemistry Letters, 2002, vol. 12, # 20, p. 2989 - 2992
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