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CAS 16650-55-8

4-Bromo-1-naphthoic Acid TCI B4949

4-Bromo-1-naphthoic Acid TCI B4949

Chemical Identity

CAS No.
16650-55-8
PubChem
CID 282591·SID 354333942
Formula
C11H7BrO2
Molecular weight
251.08 g/mol
Purity
>98.0%(GC)(T)
Reference databases
ECHA
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
4-bromonaphthalene-1-carboxylic acid
SMILES
C1=CC=C2C(=C1)C(=CC=C2Br)C(=O)O
InChIKey
FIJIPZQZVLCOMB-UHFFFAOYSA-N
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4-Bromo-1-naphthoic Acid is a chemical compound widely used as a foundational material in various laboratory reactions. It serves as a building block in organic synthesis, offering versatility in chemical transformations. Its aromatic structure contributes to its reactivity, making it a valuable reagent in synthetic pathways. This compound is commonly utilized in research settings to develop complex molecules, including pharmaceuticals and industrial chemicals. Its presence in laboratory workflows highlights its importance in advancing chemical innovation.

The compound’s reactivity stems from its bromo group, which influences its chemical behavior. This group enhances its participation in substitution and electrophilic reactions, making it suitable for hydrolysis, esterification, and nucleophilic substitution. Its stability under specific conditions ensures reliable performance in controlled environments. These properties make it a preferred choice for chemists seeking to synthesize compounds with tailored functionalities.

In Indonesian laboratories, 4-Bromo-1-naphthoic Acid is frequently used in organic chemistry research, particularly in projects involving the synthesis of bioactive compounds. It is also found in pharmacological and food chemistry studies due to its potential in developing compounds with specific biological activities. Its role in laboratory research underscores its significance as a key reagent in chemical innovation.

  • Organic synthesis projects benefit from this compound’s reactivity and structural versatility, enabling the creation of complex molecules.
  • Pharmaceutical research utilizes its ability to participate in substitution reactions, aiding in the development of new drug compounds.
  • Food chemistry studies leverage its potential in synthesizing compounds with specific functional properties.
  • Bioactive compound synthesis relies on its reactivity, making it ideal for creating molecules with targeted biological effects.
  • Industrial chemical production benefits from its stability and reactivity, supporting the development of various chemical products.

Brand TCI
CAS number 16650-55-8
Molecular formula —
Purity —
Category Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes Available in standard laboratory quantities
Physical form Solid
Storage Store in a cool, dry place away from direct sunlight

This compound should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to use airtight containers to prevent moisture exposure, which could affect its reactivity. Laboratory personnel should handle it with care, using appropriate personal protective equipment such as gloves and safety goggles. Due to its reactivity, it should be kept away from incompatible substances like strong oxidizers. Proper ventilation is essential when working with this material to minimize inhalation risks. Following these guidelines ensures safe and effective use in laboratory settings.

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