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Thermo Scientific Chemicals
4,5-Dimethoxy-2-nitrobenzoic acid, 98%
CAS: 4998-07-6 | C9H8NO6 | 226.17 g/mol
化学物質識別子
CAS4998-07-6
IUPAC Name4,5-dimethoxy-2-nitrobenzoate
Molecular FormulaC9H8NO6
InChI KeyWWCMFGBGMJAJRX-UHFFFAOYSA-M
SMILESCOC1=CC(C([O-])=O)=C(C=C1OC)[N+]([O-])=O
さらに表示
仕様
スペックシート
スペックシートFormPowder or lumps
Assay (Aqueous acid-base Titration)≥97.5 to ≤102.5%
Melting Point (clear melt)190.0-196.0?C
Appearance (Color)White to yellow
Assay (Silylated GC)≥97.5%
4,5-Dimethoxy-2-nitrobenzoic acid was used in the synthesis of 4,5-dimethoxy-2-nitrobenzamide and 6,7-dimethoxyquinazoline derivatives.
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
4,5-Dimethoxy-2-nitrobenzoic acid was used in the synthesis of 4,5-dimethoxy-2-nitrobenzamide and 6,7-dimethoxyquinazoline derivatives.
Solubility
Insoluble in water. Soluble in DMSO and methanol. Solubility in hot 1mol/L NaOH (almost transparency).
Notes
Store away from oxidizing agents. Keep the container tightly closed and place it in a cool, dry and well ventilated condition.
4,5-Dimethoxy-2-nitrobenzoic acid was used in the synthesis of 4,5-dimethoxy-2-nitrobenzamide and 6,7-dimethoxyquinazoline derivatives.
Solubility
Insoluble in water. Soluble in DMSO and methanol. Solubility in hot 1mol/L NaOH (almost transparency).
Notes
Store away from oxidizing agents. Keep the container tightly closed and place it in a cool, dry and well ventilated condition.
RUO – Research Use Only
General References:
- P A Goodman, et al. Role of tyrosine kinases in induction of the c-jun proto-oncogene in irradiated B-lineage lymphoid cells.J. Biol. Chem.,1998,273(28), 17742-17748.
- R K Narla, et al. 4-(3'-Bromo-4'hydroxylphenyl)-amino-6,7-dimethoxyquinazoline: a novel quinazoline derivative with potent cytotoxic activity against human glioblastoma cells.Clin Cancer Res.,1998,4(6), 1405-1414.