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CAS 164014-95-3

1,4-Benzodioxane-6-boronic Acid (contains varying amounts of Anhydride) TCI B4181

1,4-Benzodioxane-6-boronic Acid (contains varying amounts of Anhydride) TCI B4181

Chemical Identity

CAS No.
164014-95-3
PubChem
CID 2776178·SID 253661132
Formula
C8H9BO4
Molecular weight
179.97 g/mol
Reference databases
ECHA
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
2,3-dihydro-1,4-benzodioxin-6-ylboronic acid
SMILES
B(C1=CC2=C(C=C1)OCCO2)(O)O
InChIKey
SQDUGGGBJXULJR-UHFFFAOYSA-N
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1,4-Benzodioxane-6-boronic Acid is a chemical compound widely used in organic reactions, particularly in the synthesis of complex molecules. This reagent plays a crucial role in laboratory settings where the formation of new chemical bonds and the creation of heterocyclic compounds are required. Its unique molecular structure enables it to act as a versatile reactant or reagent in various chemical processes. Due to its stability and controlled reactivity, it is a favored choice among researchers in multiple fields of chemistry.

The compound’s chemical properties, including its boronic acid group and oxygen-containing ring structure, make it highly reactive under appropriate reaction conditions. These features allow it to participate effectively in substitution reactions and bond formation, making it suitable for a wide range of synthetic applications. Its ability to maintain stability under certain conditions also contributes to its reliability in laboratory experiments.

In Indonesian laboratories, 1,4-Benzodioxane-6-boronic Acid is commonly used in organic chemistry research, especially in academic institutions and research centers. It is a key component in the development of new chemical compounds and is frequently employed in studies involving complex molecule synthesis. Its availability and effectiveness make it an essential reagent in the chemical research landscape of Indonesia.

TCI brochures (PDF)

  • Organic synthesis for the creation of complex molecules due to its reactivity and structural versatility.
  • Heterocyclic compound formation through its ability to participate in bond-building reactions.
  • Substitution reactions where the boronic acid group facilitates selective chemical transformations.
  • Research in medicinal chemistry for the development of pharmaceutical compounds.
  • Analytical applications in chemical characterization and reactivity studies.

Brand TCI
CAS number 164014-95-3
Molecular formula —
Purity —
Category Chemistry > Organometallic Reagents > Organoboron [Organometallic Reagents]
Pack sizes As available from supplier
Physical form Solid or liquid depending on formulation
Storage Store in a cool, dry place away from moisture and direct sunlight

This material should be stored in a cool, dry place, away from moisture and direct sunlight to maintain its stability and reactivity. It is recommended to use airtight containers to prevent exposure to air and humidity, which may affect its chemical integrity. Proper labeling and storage in a designated chemical storage area are essential to ensure safety. Always handle with care, using appropriate personal protective equipment such as gloves and goggles. Avoid contact with incompatible substances and ensure good ventilation in the workspace to minimize any potential risks.

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