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Catalog Number:
29296
CAS Number:
126759-30-6
Ester méthylique de l'acide 3-bromo-4-nitrobenzoïque
Purity:
≥ 98 % (dosage)
Synonym(s):
3-bromo-4-nitrobenzoate de méthyle
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Product Information

3-Bromo-4-nitrobenzoic acid methyl ester is a versatile compound with significant applications in organic synthesis and pharmaceutical development. This compound, also known as methyl 3-bromo-4-nitrobenzoate, features a bromine and nitro group that enhance its reactivity, making it an ideal intermediate for the synthesis of various biologically active molecules. Researchers utilize this compound in the preparation of novel pharmaceuticals, agrochemicals, and dyes, leveraging its unique properties to create complex structures efficiently.

Moreover, its ability to undergo various chemical transformations allows for the development of derivatives that can be tailored for specific applications, such as in medicinal chemistry for drug discovery. The compound's stability and ease of handling further contribute to its appeal in laboratory settings, ensuring that it meets the rigorous demands of both academic and industrial research. With its broad utility and potential for innovation, 3-Bromo-4-nitrobenzoic acid methyl ester stands out as a valuable asset for professionals in the chemical and pharmaceutical industries.

Synonyms
3-bromo-4-nitrobenzoate de méthyle
CAS Number
126759-30-6
Purity
≥ 98 % (dosage)
Molecular Formula
C8H6BrNO4
Molecular Weight
260.04
MDL Number
MFCD11045599
PubChem ID
21812750
Melting Point
72-77 °C
Appearance
Poudre blanche à jaune
Conditions
Magasin chez RT
General Information
Synonyms
3-bromo-4-nitrobenzoate de méthyle
CAS Number
126759-30-6
Purity
≥ 98 % (dosage)
Molecular Formula
C8H6BrNO4
Molecular Weight
260.04
MDL Number
MFCD11045599
PubChem ID
21812750
Melting Point
72-77 °C
Appearance
Poudre blanche à jaune
Conditions
Magasin chez RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

3-Bromo-4-nitrobenzoic acid methyl ester is widely utilized in research focused on:

  • Synthetic Chemistry: This compound serves as a key intermediate in the synthesis of various pharmaceuticals and agrochemicals, enabling researchers to develop new compounds with desired biological activities.
  • Drug Development: Its unique structure allows for modifications that can lead to the discovery of novel drug candidates, particularly in targeting specific diseases such as cancer and bacterial infections.
  • Material Science: The compound can be used in the formulation of advanced materials, including polymers and coatings, which benefit from its chemical stability and reactivity.
  • Analytical Chemistry: It is employed as a standard in chromatographic techniques, aiding in the accurate quantification of similar compounds in complex mixtures.
  • Biochemistry: Researchers utilize this ester in biochemical assays to study enzyme activity and interactions, providing insights into metabolic pathways and potential therapeutic targets.

Citations