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CAS 21606-04-2

:

1-Methyl 3-nitro-1,2-benzenedicarboxylate

Description:
1-Methyl 3-nitro-1,2-benzenedicarboxylate, with the CAS number 21606-04-2, is an organic compound characterized by its aromatic structure and the presence of both nitro and carboxylate functional groups. This compound features a methyl group and a nitro group attached to a benzene ring that also contains two carboxylate groups in the 1 and 2 positions. The nitro group is known for its electron-withdrawing properties, which can influence the reactivity and stability of the compound. Typically, such compounds exhibit moderate solubility in organic solvents and may have limited solubility in water due to their hydrophobic aromatic structure. The presence of multiple functional groups suggests potential applications in organic synthesis, particularly in the development of pharmaceuticals or agrochemicals. Additionally, the compound's reactivity can be influenced by the positions of the substituents on the benzene ring, making it a subject of interest in studies related to electrophilic aromatic substitution reactions. Safety data should be consulted for handling and storage, as nitro compounds can be sensitive and potentially hazardous.
Formula:C9H7NO6
InChI:InChI=1S/C9H7NO6/c1-16-9(13)5-3-2-4-6(10(14)15)7(5)8(11)12/h2-4H,1H3,(H,11,12)
InChI key:InChIKey=DJMQLZPEBHSABD-UHFFFAOYSA-N
SMILES:C(O)(=O)C1=C(C(OC)=O)C=CC=C1N(=O)=O
Synonyms:
  • 1-Methyl 3-nitro-1,2-benzenedicarboxylate
  • 1-Methyl-3-nitrophthalate
  • 2-(Methoxycarbonyl)-6-Nitrobenzoic Acid
  • 3-Nitro-1,2-Benzenedi-Carboxylic Acid Monomethyl Ester
  • 3-nitro-2-Carboxyl methyl benzoate
  • Methyl 3-Nitro-2-Carboxyl Benzoate
  • Methyl-2-Carboxy-3-Nitrobenzoate
  • Phthalic acid, 3-nitro-, 1-methyl ester
  • 1,2-Benzenedicarboxylic acid, 3-nitro-, 1-methyl ester
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