methyl 4-(1-(tert-butoxycarbonyl)ethyl)benzoate

methyl 4-(1-(tert-butoxycarbonyl)ethyl)benzoate

(S)-3-(1-(tert-butoxycarbonyl)ethyl)benzoic acid

(S)-3-(1-(tert-butoxycarbonyl)ethyl)benzoic acid

methyl 3-amino-4,6-dibromo-2-methylbenzoate

$225.00
CAS No.: 119916-05-1
Catalog No.: 193075
Purity: 95%
MF: C9H9Br2NO2
MW: 322.984
Storage: 2-8 degree Celsius
SMILES: NC=1C(=C(C(=O)OC)C(=CC1Br)Br)C
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methyl 3-amino-4,6-dibromo-2-methylbenzoate; CAS No.: 119916-05-1; methyl 3-amino-4,6-dibromo-2-methylbenzoate. PROPERTIES: This compound presents as a white crystalline powder with molecular formula C9H8Br2N2O2 and a molecular weight of 340.98 g/mol. It demonstrates a melting point in the range of 128-132 C and shows moderate solubility in common organic solvents like methanol and ethyl acetate. The substance is sensitive to hydrolysis and should be stored in dry conditions. Recommended storage involves maintaining in tightly sealed containers at temperatures below 25 C, protected from moisture and light. When handling, standard laboratory safety protocols should be followed, including the use of protective gloves and eye wear, as methyl 3-amino-4,6-dibromo-2-methylbenzoate may cause skin irritation. The amino group requires careful handling in strongly acidic environments. APPLICATIONS: In the pharmaceutical industry, methyl 3-amino-4,6-dibromo-2-methylbenzoate serves as an intermediate for synthesizing non-steroidal anti-inflammatory drugs (NSAIDs), as described in medicinal chemistry literature focusing on benzoate derivatives. Its bromo substituents enable participation in cross-coupling reactions for constructing biaryl systems. Additionally, this compound functions as a building block for preparing agrochemicals with fungicidal activities through coupling reactions. Academic research has explored its potential in metal coordination chemistry for creating luminescent sensors, as reported in inorganic chemistry journals. The benzoate ring system also facilitates formation of metal-organic frameworks (MOFs), making it valuable for gas storage applications in materials science, as evidenced by studies in crystallography publications.

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