| Identification | More | [Name]
2-AMINO-3-METHOXYBENZOIC ACID | [CAS]
3177-80-8 | [Synonyms]
2-AMINO-3-METHOXYBENZOIC ACID
2-AMINO-M-ANISIC ACID
3-METHOXYANTHRANILIC ACID
O-ANISIDINE-6-CARBOXYLIC ACID
Benzoic acid, 2-amino-3-methoxy-
2-AMINO-3-METHOXYBENZOIC ACID 99+% | [Molecular Formula]
C8H9NO3 | [MDL Number]
MFCD00075178 | [Molecular Weight]
167.16 | [MOL File]
3177-80-8.mol |
| Chemical Properties | Back Directory | [Melting point ]
169-170 °C (lit.) | [Boiling point ]
333.9±27.0 °C(Predicted) | [density ]
1.303±0.06 g/cm3(Predicted) | [storage temp. ]
Keep in dark place,Sealed in dry,Room Temperature | [solubility ]
DMSO (Slightly), Methanol (Slightly) | [form ]
Powder | [pka]
4.82±0.10(Predicted) | [color ]
White to yellow to brown | [CAS DataBase Reference]
3177-80-8(CAS DataBase Reference) |
| Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S37/39:Wear suitable gloves and eye/face protection . | [WGK Germany ]
3
| [HS Code ]
29225090 |
| Hazard Information | Back Directory | [Chemical Properties]
White to light brown crystals or powder | [Uses]
2-Amino-3-methoxybenzoic Acid is used in the preparation of CDK1/cyclin B inhibitors for application towards antitumor treatment. In addition, it is used in the synthesis of Alogliptin, an inhibitor o
f dipeptidy peptidase, which aids in the lowering of blood-glucose for potential treatment of diabetes. | [Definition]
ChEBI: 3-methoxyanthranilic acid is an aminobenzoic acid that is anthranilic acid in which the hydrogen at position 3 is substituted by a methoxy group. It is a metabolite of kynurenine. It has a role as a mammalian metabolite. It is a member of benzoic acids and an aminobenzoic acid. It is functionally related to an anthranilic acid. It is a conjugate acid of a 3-methoxyanthranilate. | [Synthesis Reference(s)]
The Journal of Organic Chemistry, 63, p. 6797, 1998 DOI: 10.1021/jo972158g |
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