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Methyl 2-hydroxy-5-nitrobenzoate, 98%, Thermo Scientific Chemicals
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Catalog number B25278.30
also known as B25278-30
Price (EUR)/ Each
446,78
Online exclusive
502.00 Save 55,22 (11%)
-
Quantity:
250 g
Price (EUR)/ Each
446,78
Online exclusive
502.00 Save 55,22 (11%)
Methyl 2-hydroxy-5-nitrobenzoate, 98%, Thermo Scientific Chemicals
Catalog numberB25278.30
Price (EUR)/ Each
446,78
Online exclusive
502.00 Save 55,22 (11%)
-
Chemical Identifiers
CAS17302-46-4
IUPAC Name2-(methoxycarbonyl)-4-nitrobenzen-1-olate
Molecular FormulaC8H6NO5
InChI KeyUUBFELFUKFJSRD-UHFFFAOYSA-M
SMILESCOC(=O)C1=CC(=CC=C1[O-])[N+]([O-])=O
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Specifications
Specification Sheet
Specification SheetAppearance (Color)White to pale cream to cream to orange
Assay (GC)≥97.5%
Melting Point (clear melt)113.0-119.0?C
FormCrystals or powder or crystalline powder
Methyl 2-hydroxy-5-nitrobenzoate is used as pharmaceutical intermediate.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
Methyl 2-hydroxy-5-nitrobenzoate is used as pharmaceutical intermediate.
Solubility
Insoluble in water.
Notes
Stable under recommended storage conditions. Incompatible with oxidizing agents.
Methyl 2-hydroxy-5-nitrobenzoate is used as pharmaceutical intermediate.
Solubility
Insoluble in water.
Notes
Stable under recommended storage conditions. Incompatible with oxidizing agents.
RUO – Research Use Only
General References:
- John McGinley; Vickie McKee; Hans Toftlund; John M.D.Walsh. Unusual metal coordination chemistry from an amino-amide derivative of 4-nitrophenol, a surprising ligand. Dalton Trans. 2009, (39), 8406-8412.
- David R.Edwards; Alexei A.Neverov; R.Stan Brown. Dissociative solvolytic cleavage of methyl (ortho-carboxymethyl)aryl phosphate diesters mediated by Yb3+ in methanol gives a 1012-fold rate acceleration attributable to leaving group assistance. J. Am. Chem. Soc. 2009, 131,(1), 368-377.