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TCI

CAS 475250-52-3

2-(4-Methoxybenzyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane TCI M2071

2-(4-Methoxybenzyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane TCI M2071

Chemical Identity

CAS No.
475250-52-3
PubChem
CID 12012759·SID 87561474
Formula
C14H21BO3
Molecular weight
248.13 g/mol
Purity
>97.0%(GC)(T)
Reference databases
ECHA
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
2-[(4-methoxyphenyl)methyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
SMILES
B1(OC(C(O1)(C)C)(C)C)CC2=CC=C(C=C2)OC
InChIKey
HPNLRRQVSZVKHY-UHFFFAOYSA-N
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2-(4-Methoxybenzyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is an organoboron compound widely used in chemical laboratories for its versatility in organic synthesis. This compound plays a crucial role in various reactions, particularly in coupling reactions such as the Suzuki-Miyaura reaction, which is essential for the creation of complex organic molecules. Its unique structure, combining a boron core with aromatic and methoxy groups, makes it a valuable reagent for chemists seeking to synthesize a wide range of compounds with specific chemical properties.

The compound's chemical stability under controlled conditions, along with its sensitivity to moisture and oxidation, makes it a preferred choice for specialized applications. Its molecular complexity allows for highly specific and selective reactions, which is vital in the development of pharmaceuticals and advanced materials. The solid form of the compound also facilitates ease of handling and use in laboratory settings, contributing to its popularity among researchers.

In Indonesian laboratories, this compound is commonly used in organic chemistry research, especially in the development of pharmacological compounds and innovative materials. Researchers at educational and research institutions rely on this reagent for its reliability and effectiveness in complex chemical processes. Its availability and performance make it a go-to choice for those working on advanced synthetic pathways.

TCI brochures (PDF)

  • Organic synthesis applications benefit from this compound's ability to participate in selective coupling reactions, enhancing the efficiency of complex molecule creation.
  • Pharmaceutical research utilizes this reagent for the synthesis of drug molecules, leveraging its reactivity in cross-coupling processes.
  • Material science projects incorporate this compound to develop novel materials with tailored chemical properties through controlled reaction conditions.
  • Analytical chemistry experiments use this compound as a reference standard for studying reaction mechanisms and chemical behavior.
  • Environmental studies employ this reagent to investigate the fate and transformation of organic compounds in different chemical environments.

Brand TCI
CAS number 475250-52-3
Molecular formula —
Purity —
Category Chemistry > Organometallic Reagents > Organoboron [Organometallic Reagents]
Pack sizes Available in standard laboratory quantities
Physical form Solid
Storage —

This compound should be stored in a cool, dry place away from moisture and oxidizing agents to maintain its chemical integrity. It is recommended to use airtight containers made of materials that do not react with organoboron compounds, such as glass or high-density polyethylene. Due to its sensitivity to humidity, it is essential to handle the compound in a controlled environment and ensure that storage conditions are consistent with laboratory safety standards. Proper labeling and storage practices are crucial to prevent accidental exposure and ensure the compound remains effective for its intended applications.

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