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Methyl 2-methyl-3-nitrobenzoate, 97%
CAS: 59382-59-1 | C9H9NO4 | 195.17 g/mol
$70.45 - $263.03
Chemical Identifiers
| CAS | 59382-59-1 |
|---|---|
| Molecular Formula | C9H9NO4 |
| Molecular Weight (g/mol) | 195.17 |
| MDL Number | MFCD00082564 |
| InChI Key | CRZGFIMLHZTLGT-UHFFFAOYSA-N |
| Synonym | benzoic acid, 2-methyl-3-nitro-, methyl ester, methyl 3-nitro-o-toluate, 2-methyl-3-nitrobenzoic acid methyl ester, methyl 3-nitro-2-methylbenzoate, 3-nitro-o-toluic acid methyl ester, 2-methyl-3-nitromethylbenzoate, pubchem10933, acmc-1awh8, ksc495s1j, methyl2-methyl-3-nitrobenzoate |
| PubChem CID | 601165 |
| IUPAC Name | methyl 2-methyl-3-nitrobenzoate |
| SMILES | COC(=O)C1=CC=CC(=C1C)[N+]([O-])=O |
| Catalog Number | Mfr. No. | Quantity | Price | Quantity | |||||
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| Catalog Number | Mfr. No. | Quantity | Price | Quantity | |||||
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AAH6024206
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Thermo Scientific Chemicals
H6024206 |
5 g |
Each for $70.45
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AAH6024214
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Thermo Scientific Chemicals
H6024214 |
25 g |
Each for $263.03
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Description
Methyl 2-methyl-3-nitrobenzoate may be used in the synthesis of methyl indole-4-carboxylate, 5-aminoisoquinolin-1(2H)-one, 5-nitroisocoumarin and [2-(4-fluorophenyl)-1H-indol-4-yl]-1-pyrrolidinylmethanone. It may also be used in the preparation of substituted nitrostyrene benzoic acids, via reaction with aromatic aldehydes in the presence of DBU in DMSO; and 4-(hydroxymethyl)-1-tosylindole, via Batcho-Leimgruber modification of the Reissert indole synthesis.
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.
ApplicationsMethyl 2-methyl-3-nitrobenzoate may be used in the synthesis of methyl indole-4-carboxylate, 5-aminoisoquinolin-1(2H)-one, 5-nitroisocoumarin and [2-(4-fluorophenyl)-1H-indol-4-yl]-1-pyrrolidinylmethanone. It may also be used in the preparation of substituted nitrostyrene benzoic acids, via reaction with aromatic aldehydes in the presence of DBU in DMSO; and 4-(hydroxymethyl)-1-tosylindole, via Batcho-Leimgruber modification of the Reissert indole synthesis.
Solubility
Soluble in methanol.
Notes
Stable under recommended storage conditions. Incompatible with oxidizing agents and heat.
Chemical Identifiers
| 59382-59-1 | |
| 195.17 | |
| CRZGFIMLHZTLGT-UHFFFAOYSA-N | |
| 601165 | |
| COC(=O)C1=CC=CC(=C1C)[N+]([O-])=O |
| C9H9NO4 | |
| MFCD00082564 | |
| benzoic acid, 2-methyl-3-nitro-, methyl ester, methyl 3-nitro-o-toluate, 2-methyl-3-nitrobenzoic acid methyl ester, methyl 3-nitro-2-methylbenzoate, 3-nitro-o-toluic acid methyl ester, 2-methyl-3-nitromethylbenzoate, pubchem10933, acmc-1awh8, ksc495s1j, methyl2-methyl-3-nitrobenzoate | |
| methyl 2-methyl-3-nitrobenzoate |
Specifications
| 59382-59-1 | |
| C9H9NO4 | |
| 5 g | |
| benzoic acid, 2-methyl-3-nitro-, methyl ester, methyl 3-nitro-o-toluate, 2-methyl-3-nitrobenzoic acid methyl ester, methyl 3-nitro-2-methylbenzoate, 3-nitro-o-toluic acid methyl ester, 2-methyl-3-nitromethylbenzoate, pubchem10933, acmc-1awh8, ksc495s1j, methyl2-methyl-3-nitrobenzoate | |
| CRZGFIMLHZTLGT-UHFFFAOYSA-N | |
| methyl 2-methyl-3-nitrobenzoate | |
| 601165 | |
| 97% |
| 62°C to 65°C | |
| MFCD00082564 | |
| 1964020 | |
| Soluble in methanol. | |
| COC(=O)C1=CC=CC(=C1C)[N+]([O-])=O | |
| 195.17 | |
| 195.17 | |
| Methyl 2-methyl-3-nitrobenzoate |
Safety and Handling
TSCA : No
Recommended Storage : Ambient temperatures
RUO – Research Use Only