Description
Dimethyl 3-aminobenzene-1,2-dicarboxylate (CAS: 34529-06-1) is a high-purity chemical compound with the molecular formula C10H11NO4. This ester derivative of 3-aminophthalic acid is widely utilized in organic synthesis, pharmaceutical research, and material science applications. The compound features a benzene ring substituted with an amino group and two methyl ester functionalities at the 1,2-positions, making it a versatile intermediate for further functionalization. With a molecular weight of 209.20 g/mol, it is supplied as a crystalline solid with excellent stability under standard laboratory conditions. Our product undergoes rigorous quality control to ensure ≥98% purity (HPLC), making it ideal for sensitive research applications.
Properties
- CAS Number: 34529-06-1
- Complexity: 254
- IUPAC Name: dimethyl 3-aminobenzene-1,2-dicarboxylate
- InChI: InChI=1S/C10H11NO4/c1-14-9(12)6-4-3-5-7(11)8(6)10(13)15-2/h3-5H,11H2,1-2H3
- InChI Key: VEJKSNHPNFHCLF-UHFFFAOYSA-N
- Exact Mass: 209.06880783
- Molecular Formula: C10H11NO4
- Molecular Weight: 209.20
- SMILES: COC(=O)C1=C(C(=CC=C1)N)C(=O)OC
- Topological: 78.6
- Monoisotopic Mass: 209.06880783
- Synonyms: 34529-06-1, dimethyl 3-aminobenzene-1,2-dicarboxylate, DTXSID80539363, DTXCID10490150, Dimethyl 3-aminophthalate, 1,2-dimethyl 3-aminobenzene-1,2-dicarboxylate, 3-Amino-phthalic acid dimethyl ester, 3-AMINO-1,2-PHTHALIC ACID, DIMETHYL ESTER, MFCD09029586, DIMETHYL 3-AMINO-1,2-BENZENEDICARBOXYLATE, methyl 2-amino-6-(methoxycarbonyl)benzoate, 3-Aminophthalic Acid Dimethyl Ester, 1,2-Benzenedicarboxylic acid, 3-amino-, dimethyl ester, Dimethyl3-aminophthalate, methyl 3-amino phthalate, SCHEMBL60709, VEJKSNHPNFHCLF-UHFFFAOYSA-N, ALBB-025534, SBB072566, STL433375, AKOS015962615, CS-W019874, PB31341, DS-15898, SY097862, DB-069019, Methyl 3-amino-2-(methoxycarbonyl)benzoate, Methyl-3-amino-2-(methoxycarbonyl)benzoate, ST45028468, 1,2-benzenedicarboxylic acid, 3-amino-, dimethyl ester, hydrochloride
Dimethyl 3-aminobenzene-1,2-dicarboxylate serves as a key precursor in the synthesis of heterocyclic compounds, fluorescent dyes, and pharmaceutical intermediates. Researchers employ it in Suzuki coupling reactions and as a building block for metal-organic frameworks (MOFs). Its amino and ester groups allow for selective modifications in peptide-mimetic studies. The compound is particularly valuable in developing novel chemiluminescent probes for analytical chemistry.
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