• 2,3-Dihydrobenzofuran-5-boronic Acid (contains varying amounts of Anhydride) (CAS 227305-69-3) - TCI D4711 - AMI Scientific
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TCI

CAS 227305-69-3

2,3-Dihydrobenzofuran-5-boronic Acid (contains varying amounts of Anhydride) TCI D4711

2,3-Dihydrobenzofuran-5-boronic Acid (contains varying amounts of Anhydride) TCI D4711

Chemical Identity

CAS No.
227305-69-3
Formula
C8H9BO3
Molecular weight
163.97 g/mol
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
2,3-dihydro-1-benzofuran-5-ylboronic acid
SMILES
B(C1=CC2=C(C=C1)OCC2)(O)O
InChIKey
ZIXLJHSFAMVHPC-UHFFFAOYSA-N
MDL
MDL02681979
PubChem
CID 2773380
Rp 1.936.200,00
Rp 1.936.200,00
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2,3-Dihydrobenzofuran-5-boronic Acid is a chemical compound widely used in organic reactions, particularly in the synthesis of heterocyclic compounds and boron-containing molecules. This compound plays a crucial role in laboratory settings due to its unique reactivity and structural complexity. The presence of a boron atom makes it a versatile reagent for various chemical transformations, especially in coupling reactions. Its ability to form stable intermediates under controlled conditions makes it an essential tool for chemists working on complex molecular structures.

This compound is preferred for its high reactivity towards organic halides and transition metals, which facilitates the formation of new chemical bonds. Its stability under controlled laboratory conditions ensures consistent performance in synthetic processes. The compound's ability to participate in a wide range of reactions, including Suzuki and Stille couplings, makes it a valuable asset in modern organic synthesis. Its versatility and reliability make it a popular choice among researchers in both academic and industrial settings.

In Indonesian laboratories, 2,3-Dihydrobenzofuran-5-boronic Acid is commonly used in organic chemistry research, especially in projects involving the synthesis of heterocyclic compounds and boron-based molecules. It is frequently employed in the development of new pharmaceuticals and materials due to its reactivity and compatibility with various synthetic methodologies. Its application in these contexts highlights its importance in advancing chemical research and innovation in the region.

  • Organic synthesis of heterocyclic compounds due to its reactivity and structural versatility.
  • Coupling reactions such as Suzuki and Stille for forming carbon-carbon bonds.
  • Development of boron-containing compounds for pharmaceutical and material science applications.
  • Research in transition metal catalysis where boronic acid derivatives are essential.
  • Synthesis of aromatic and phenolic derivatives through functional group transformations.

Brand TCI
CAS number 227305-69-3
Molecular formula —
Purity —
Category Chemistry > Organometallic Reagents > Organoboron [Organometallic Reagents]
Pack sizes As per supplier specifications
Physical form Solid (as per standard product description)
Storage Store in a cool, dry place away from moisture and direct sunlight.

This compound should be stored in a cool, dry environment to maintain its stability and reactivity. It is recommended to use airtight containers to prevent exposure to moisture and air, which can affect its chemical integrity. Due to its reactivity, it should be handled with appropriate personal protective equipment, including gloves and safety goggles. Proper ventilation is essential when working with this compound to minimize inhalation risks. It should not be stored near incompatible substances such as strong oxidizers or acids. Regular monitoring of storage conditions ensures the compound remains suitable for use in laboratory applications.

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