CAS 206548-14-3
:Methyl 2-amino-5-bromo-3-methylbenzoate
Description:
Methyl 2-amino-5-bromo-3-methylbenzoate, with the CAS number 206548-14-3, is an organic compound that belongs to the class of benzoate esters. It features a methyl ester functional group, which contributes to its solubility in organic solvents. The presence of the amino group (-NH2) and the bromo substituent (Br) on the aromatic ring indicates that it may exhibit interesting reactivity, particularly in nucleophilic substitution reactions. The compound is likely to be a solid at room temperature, with a specific melting point that can vary based on purity and crystalline form. Its structure suggests potential applications in pharmaceuticals or as an intermediate in organic synthesis, particularly in the development of biologically active compounds. Additionally, the bromine atom may impart unique properties, such as increased lipophilicity or altered electronic characteristics, which can influence its behavior in chemical reactions and interactions with biological systems. Safety data should be consulted for handling and storage, as halogenated compounds can pose specific health and environmental risks.
Formula:C9H10BrNO2
InChI:InChI=1S/C9H10BrNO2/c1-5-3-6(10)4-7(8(5)11)9(12)13-2/h3-4H,11H2,1-2H3
InChI key:InChIKey=NVJKMGDNYCDLGR-UHFFFAOYSA-N
SMILES:C(OC)(=O)C1=C(N)C(C)=CC(Br)=C1
Synonyms:- Benzoic acid, 2-amino-5-bromo-3-methyl-, methyl ester
- Methyl 2-amino-5-bromo-3-methylbenzoate
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Found 4 products.
Benzoic acid, 2-amino-5-bromo-3-methyl-, methyl ester
CAS:Formula:C9H10BrNO2Purity:98%Color and Shape:SolidMolecular weight:244.0852Methyl 2-amino-5-bromo-3-methylbenzoate
CAS:<p>Methyl 2-amino-5-bromo-3-methylbenzoate</p>Purity:≥95%Color and Shape:PowderMolecular weight:244.09g/molMethyl 2-Amino-5-bromo-3-methylbenzoate
CAS:Formula:C9H10BrNO2Purity:95%Color and Shape:SolidMolecular weight:244.088Methyl 2-amino-5-bromo-3-methylbenzoate
CAS:<p>Methyl 2-amino-5-bromo-3-methylbenzoate is an analog of the amino acid threonine. It has been shown to have medicinal properties in humans and has been used as a probe to study cellular functions. In addition, it is part of the family of molecule inhibitors that function by binding to catalytic sites on enzymes. Methyl 2-amino-5-bromo-3-methylbenzoate inhibits cellular functions by interfering with protein synthesis and altering cellular physiology.</p>Formula:C9H10NO2BrPurity:Min. 95%Molecular weight:244.08 g/mol



