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Catalog Number:
18884
CAS Number:
16650-63-8
3-Bromo-naphthalene-1-carboxylic acid methyl ester
Purity:
≥ 96% (HPLC)
Synonym(s):
Methyl 3-bromonaphthalene-1-carboxylate
Documents
$65.40 /100MG
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Product Information

3-Bromo-naphthalene-1-carboxylic acid methyl ester is a versatile compound widely utilized in organic synthesis and pharmaceutical research. This compound, known for its unique bromine substitution, serves as an essential building block in the synthesis of various biologically active molecules. Its structure allows for diverse functionalization, making it a valuable intermediate in the development of agrochemicals, dyes, and pharmaceuticals. Researchers appreciate its role in facilitating reactions such as cross-coupling and nucleophilic substitutions, which are critical in the creation of complex organic compounds.

The compound's methyl ester functionality enhances its solubility and reactivity, making it suitable for a range of applications in both laboratory and industrial settings. Its use in the synthesis of naphthalene derivatives has been particularly notable in the development of novel materials and therapeutic agents. With its favorable properties and broad applicability, 3-Bromo-naphthalene-1-carboxylic acid methyl ester stands out as a key reagent for chemists looking to innovate in their respective fields.

Synonyms
Methyl 3-bromonaphthalene-1-carboxylate
CAS Number
16650-63-8
Purity
≥ 96% (HPLC)
Molecular Formula
C12H9BrO2
Molecular Weight
265.11
MDL Number
MFCD06658478
PubChem ID
11311609
Appearance
White to off-white crystalline powder
Conditions
Store at 0-8 °C
General Information
Synonyms
Methyl 3-bromonaphthalene-1-carboxylate
CAS Number
16650-63-8
Purity
≥ 96% (HPLC)
Molecular Formula
C12H9BrO2
Molecular Weight
265.11
MDL Number
MFCD06658478
PubChem ID
11311609
Appearance
White to off-white crystalline powder
Conditions
Store at 0-8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

3-Bromo-naphthalene-1-carboxylic acid methyl ester is widely utilized in research focused on:

  • Synthesis of Pharmaceuticals: This compound serves as an important intermediate in the synthesis of various pharmaceutical agents, enhancing the development of new medications.
  • Organic Electronics: It is used in the production of organic semiconductors, contributing to advancements in flexible electronics and organic light-emitting diodes (OLEDs).
  • Fluorescent Dyes: The compound is utilized in creating fluorescent dyes for biological imaging, aiding researchers in visualizing cellular processes.
  • Material Science: It plays a role in developing polymeric materials with specific properties, such as improved thermal stability and mechanical strength.
  • Environmental Applications: This chemical is explored for its potential in creating environmentally friendly pesticides, helping to reduce the ecological impact of traditional chemicals.

Citations