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62456-32-0

1-Hydroxy-8-bromonaphthalene

Catalog#: AR00EGXR  |   CAS#: 62456-32-0  |   MDL#: MFCD17012355  |   MF: C10H7BrO  |   MW: 223.066

Packsize Purity Price Availability Quantity
100mg 97% $22.00 Global Stock Buy Now Add To Cart
250mg 97% $39.00 Global Stock Buy Now Add To Cart
500mg 97% $58.00 Global Stock Buy Now Add To Cart
1g 97% $80.00 Global Stock Buy Now Add To Cart
5g 97% $240.00 Global Stock Buy Now Add To Cart
10g 97% $455.00 Global Stock Buy Now Add To Cart
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Catalog Number AR00EGXR
Chemical Name 1-Hydroxy-8-bromonaphthalene
CAS Number 62456-32-0
Molecular Formula C10H7BrO
Molecular Weight 223.066
MDL Number MFCD17012355
SMILES Oc1cccc2c1c(Br)ccc2

8-Bromo-1-naphthalenol, also known as 8-Bromonaphthol, is a versatile chemical compound widely used in various chemical synthesis processes. Its unique structure and properties make it a valuable tool for organic chemists and researchers in the field.One key application of 8-Bromo-1-naphthalenol is as a versatile building block in the synthesis of complex organic molecules. Its bromine functional group allows for various substitution reactions, making it a crucial intermediate in the preparation of different organic compounds. Chemists can utilize 8-Bromo-1-naphthalenol to introduce specific functional groups or modify existing structures, enabling the synthesis of novel materials and pharmaceuticals.Additionally, 8-Bromo-1-naphthalenol is commonly employed in the preparation of dyes, pigments, and fluorescent compounds. Its aromatic naphthalene ring system plays a vital role in the color and fluorescence properties of the resulting products. By incorporating 8-Bromo-1-naphthalenol into the molecular structure, chemists can tailor the optical and electronic properties of the final materials for various applications in industry and research.Moreover, 8-Bromo-1-naphthalenol serves as a valuable tool in bioconjugation chemistry. By functionalizing biomolecules with this compound, researchers can create bioactive conjugates for use in biological studies, drug delivery systems, and diagnostic applications. The selective reactivity of 8-Bromo-1-naphthalenol allows for controlled conjugation reactions with proteins, peptides, and other biological molecules, expanding the possibilities for designing advanced bioconjugates.Overall, 8-Bromo-1-naphthalenol's versatility and reactivity make it an indispensable reagent in chemical synthesis, materials science, and bioconjugation applications. Its ability to participate in diverse chemical transformations enables the creation of innovative compounds with tailored properties and functionalities for a wide range of scientific and industrial purposes.
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GHS Pictogram
Signal Word Warning
UN# N/A
Hazard Statements H302-H315-H319-H335
Precautionary Statements P261-P305+P351+P338
Class N/A
Packing Group N/A

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