Thermo Scientific™ (3-(Naphthalen-1-yl)phenyl)boronic acid 98%

Catalog No :

CAS Number :

Brand :

Availability :

In Stock


Formula: C₁₆H₁₃BO₂
Storage Temperature: Ambient
CAS Number: 881913-20-8

Conditions générales
Garantie satisfait ou remboursé de 30 jours
Expédition : 2-3 jours ouvrables

  • Pack Size

This combination does not exist.

Place Inquiry

This combination does not exist.

Specifications:
Application Organic Synthesis
Storage Temperature Ambient
Product Type Laboratory Chemical Forms Powder
Product Brand Thermo Fisher Scientific™, thermo Scientific
Product Grade Analytical grade Formula C₁₆H₁₃BO₂

(3-(Naphthalen-1-yl)phenyl)boronic acid is a highly pure arylboronic acid derivative used in Suzuki-Miyaura cross-coupling reactions and other palladium-catalyzed coupling strategies for building complex aromatic and heteroaromatic compounds. Featuring both naphthalene and phenyl moieties, this compound is suitable for use in pharmaceutical intermediate synthesis, organic electronics, materials science, and medicinal chemistry research.

This reagent is supplied at ≥98% purity, making it suitable for demanding synthetic applications where chemical precision is critical. It is compatible with most common organometallic reagents and reaction conditions.

Key Features

  • High purity: ≥98%
  • Supplied as a white crystalline powder
  • Ideal for Suzuki coupling and C–C bond formation
  • Useful in medicinal chemistry, OLED/organic materials synthesis, and combinatorial libraries
  • Stable under standard laboratory storage conditions
  • Available in 250 mg, 1 g, and 5 g quantities

Applications

  • Suzuki-Miyaura cross-coupling for C–C bond formation
  • Synthesis of biaryls, pharmaceutical intermediates, and aromatic frameworks
  • Ligand and catalyst development
  • Organic material synthesis (e.g., OLEDs, sensors)
  • Research in medicinal and synthetic organic chemistry

Chemical & Physical Properties

PropertySpecification
Chemical Name(3-(Naphthalen-1-yl)phenyl)boronic acid
Synonyms3-naphthalen-1-yl phenylboronic acid, 3-(1-naphthyl)benzeneboronic acid, etc.
CAS Number881913-20-8
Molecular FormulaC₁₆H₁₃BO₂
Molecular Weight248.09 g/mol
Percent Purity≥98%
Physical FormWhite powder
ColorWhite
MDL NumberMFCD11045054
PubChem CID58881077
IUPAC Name(3-naphthalen-1-ylphenyl)boronic acid
SMILESB(C1=CC(=CC=C1)C2=CC=CC3=CC=CC=C32)(O)O
InChI KeyHFXYUCJLQZCNPD-UHFFFAOYSA-N

Available Packaging Sizes

Catalog NumberQuantityPackaging
H64019.MD 250 mgGlass vial
H64019.03 1 gGlass vial
H64019.06 5 gGlass vial


Thermo Scientific™ (3-(Naphthalen-1-yl)phenyl)boronic acid, 98% is a versatile, high-purity reagent essential for modern organic synthesis and materials science. Its high purity and reliable performance make it an excellent choice for researchers involved in cross-coupling reactions, small molecule synthesis, and functional material development.

  • Pack Size:   250mg 1g 5g
Resources file not found.


Add a Review

Rate this Product  
Name *
Email *

Your Review *
20960





0

0  Reviews
(0) 
(0) 
(0) 
(0) 
(0) 

Customer Review