2-Amino-6-methylbenzoic acid, 98%, Thermo Scientific Chemicals
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2-Amino-6-methylbenzoic acid, 98%, Thermo Scientific Chemicals
2-Amino-6-methylbenzoic acid, 98%, Thermo Scientific Chemicals
2-Amino-6-methylbenzoic acid, 98%, Thermo Scientific Chemicals
Thermo Scientific Chemicals

2-Amino-6-methylbenzoic acid, 98%, Thermo Scientific Chemicals

CAS: 4389-50-8 | C8H8NO2 | 150.16 g/mol
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Catalog NumberQuantity
ALFA15187.065 g
Catalog number ALFA15187.06
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Quantity:
5 g
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Chemical Identifiers
CAS30084-90-3
IUPAC Name9H-fluorene-2-carbaldehyde
Molecular FormulaC14H10O
InChI KeyMNQGEQSXFDKAPY-UHFFFAOYSA-N
SMILESO=CC1=CC=C2C(CC3=CC=CC=C23)=C1
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SpecificationsSpecification SheetSpecification Sheet
Appearance (Color)White to pale yellow
FormPowder
Assay (GC)≥98.5%
Free acid (titration)≤1.0%
Melting Point (clear melt)80.5-86.5?C
2-Amino-6-methylbenzoic acid reacts with cyanogen bromide to prepare 2-amino-5-methyl-benzo[d][1,3]oxazin-4-one.

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
2-Amino-6-methylbenzoic acid reacts with cyanogen bromide to prepare 2-amino-5-methyl-benzo[d][1,3]oxazin-4-one.

Solubility
Soluble in methanol.

Notes
Incompatible with strong oxidizing agents and strong acids.
RUO – Research Use Only

General References:

  1. Ma, C.; Gong, G.; Liu, Z.; Ma, A.; Chen, Z. Stimulatory effects of tea supplements on the propagation of Lactobacillus casei in milk. Int. Dairy. J. 2015, 43, 1-6.
  2. Pearson, A. J.; Panda, S. N-Prolinylanthranilic acid derivatives as bifunctional organocatalysts for asymmetric aldol reactions. Tetrahedron 2011, 67 (22), 3969-3975.
  3. Wang, D.; Lin, H.; Cao, R.; Yang, S.; Chen, Q.; Hao, G.; Yang, W.; Yang, G. Synthesis and Herbicidal Evaluation of Triketone-Containing Quinazoline-2,4-diones. J. Agric. Food Chem. 2014, 62 (49), 11786-11796.