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Thermo Scientific Chemicals
Methyl 2-amino-5-bromobenzoate, 98%
CAS: 52727-57-8 | C8H8BrNO2 | 230.06 g/mol
化学物質識別子
CAS52727-57-8
仕様
スペックシート
スペックシートMelting Point68.0-74.0?C (clear to hazy)
Appearance (Color)Pale cream to cream to pale gray or pale brown
FormCrystals or powder or crystalline powder
Assay (GC)≥97.5%
Methyl 2-amino-5-bromobenzoate acts as a potential PqsD inhibitor against pseudomonas aeruginosa infections. It is also used in the preparation of hepatitis C virus NS5b RNA polymerase inhibitors. It is involved in plant growth-regulator activity.
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
Methyl 2-amino-5-bromobenzoate acts as a potential PqsD inhibitor against pseudomonas aeruginosa infections. It is also used in the preparation of hepatitis C virus NS5b RNA polymerase inhibitors. It is involved in plant growth-regulator activity.
Solubility
Soluble in water.
Notes
Light and air sensitive. Incompatible with strong oxidizing agents, strong reducing agents, acid halides, acid anhydrides, strong acids and strong bases. Store in a cool place.
Methyl 2-amino-5-bromobenzoate acts as a potential PqsD inhibitor against pseudomonas aeruginosa infections. It is also used in the preparation of hepatitis C virus NS5b RNA polymerase inhibitors. It is involved in plant growth-regulator activity.
Solubility
Soluble in water.
Notes
Light and air sensitive. Incompatible with strong oxidizing agents, strong reducing agents, acid halides, acid anhydrides, strong acids and strong bases. Store in a cool place.
RUO – Research Use Only
General References:
- Saxena, A.; Agrawal, M.; Gupta, A. Vibrational study, molecular properties and first-order molecular hyperpolarizability of Methyl 2-amino 5-bromobenzoate using DFT method. Opt. Mater. 2015, 46, 154-167.
- Grombein, C. M.; Hu, Q.; Rau, S.; Zimmer, C.; Hartmann, R. W. Heteroatom insertion into 3,4-dihydro-1H-quinolin-2-ones leads to potent and selective inhibitors of human and rat aldosterone synthase. Eur. J. Med. Chem. 2015, 90, 788-796.