ChemImpex 3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde; 98% (GC); 380151-86-0; MFCD05663827, 5G

Name: ChemImpex 3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde; 98% (GC); 380151-86-0; MFCD05663827, 5G
SKU: CMX-39883-5G
Price: 88.22 USD

List Price $88.22 Your Price $88.22

ChemImpex 3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde; 98% (GC); 380151-86-0; MFCD05663827 - CMX (Additional S&H or Hazmat Fees May Apply)

NETA PART: CMX-39883-5G

MFG.PART: 39883-5G

UNSPSC: 12350000

Manufacturer: Chem Impex International

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Description

3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This compound features a unique dioxaborolane moiety, which enhances its reactivity and stability, making it an excellent choice for researchers focusing on boron chemistry. Its structure allows for efficient incorporation into various synthetic pathways, particularly in the development of pharmaceuticals and agrochemicals. The compound has shown promise in applications such as cross-coupling reactions, which are pivotal in forming carbon-carbon bonds, thus facilitating the creation of complex organic molecules.

Moreover, the presence of the benzaldehyde functional group provides additional reactivity, allowing for further derivatization and functionalization. This characteristic is particularly beneficial for researchers looking to explore new chemical entities or optimize existing compounds. With its unique properties and practical applications, 3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde stands out as a valuable tool for both academic and industrial chemists aiming to innovate in their respective fields.

Specifications

Synonyms	3-Formylphenylboronic acid pinacol ester, 2-(3-Formylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
CAS Number	380151-86-0
Purity	≥ 98% (GC)
Molecular Formula	C₁₃H₁₇BO₃
Molecular Weight	232.09
MDL Number	MFCD05663827
PubChem ID	2760586
Melting Point	51 - 55 °C
Appearance	White to light yellow crystalline powder
Conditions	Store at RT

Safety & Regulations

Hazmat	No
Antibiotic	No
DEA-regulated	No
Warnings	-

3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde is widely utilized in research focused on:

Organic Synthesis: This compound serves as a versatile building block in the synthesis of complex organic molecules, particularly in the development of pharmaceuticals and agrochemicals.
Fluorescent Probes: It can be employed in the creation of fluorescent probes for biological imaging, aiding researchers in visualizing cellular processes in real-time.
Cross-Coupling Reactions: The compound is effective in cross-coupling reactions, such as Suzuki-Miyaura coupling, which is crucial for forming carbon-carbon bonds in various organic compounds.
Material Science: It finds applications in the development of advanced materials, including polymers and nanomaterials, enhancing their properties for electronics and coatings.
Medicinal Chemistry: Researchers utilize it in the design of new drug candidates, leveraging its unique structure to improve efficacy and reduce side effects in therapeutic applications.

Specifications

More Information
SKU	CMX-39883-5G
Supplier Part Number	39883-5G
UM	EA
UNSPSC	12350000
Manufacturer	Chem Impex International
Temperature	Store at RT
ProductLine	CMX
Qty	1
MinOrderQty	1
Weight	7.000000
Lead Time	5
Hazardous	N
CAS Number	380151-86-0
Energy Star	No
Green	No
Controlled	N

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ChemImpex 3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde; 98% (GC); 380151-86-0; MFCD05663827, 5G

Specifications

Safety & Regulations

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