1184259-08-2

Basic information

• Product Name: 3-ForMyl-4-nitrophenyl boronicacid pinacol ester
• Synonyms: 3-ForMyl-4-nitrophenyl boronicacid pinacol ester;2-Nitro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde
• CAS NO: 1184259-08-2
• Molecular Formula: C₁₃H₁₆BNO₅
• Molecular Weight: 295.09612
• EINECS: -0
• Mol File: 1184259-08-2.mol

Chemical Properties

• Appearance: /
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• CAS DataBase Reference: 3-ForMyl-4-nitrophenyl boronicacid pinacol ester(CAS DataBase Reference)
• NIST Chemistry Reference: 3-ForMyl-4-nitrophenyl boronicacid pinacol ester(1184259-08-2)
• EPA Substance Registry System: 3-ForMyl-4-nitrophenyl boronicacid pinacol ester(1184259-08-2)

Safety Data

• Hazardous Substances Data: 1184259-08-2(Hazardous Substances Data)

Usage

Uses

Used in Organic Synthesis:
3-Formyl-4-nitrophenyl boronic acid pinacol ester is used as a reagent for the preparation of a variety of functionalized molecules. Its versatility in organic synthesis allows for the creation of complex molecular structures.
Used in the Suzuki-Miyaura Cross-Coupling Reaction:
In the field of organic chemistry, 3-Formyl-4-nitrophenyl boronic acid pinacol ester is used as a coupling partner in the Suzuki-Miyaura cross-coupling reaction. This reaction is a powerful method for forming carbon-carbon bonds, which is essential for the synthesis of various organic compounds.
Used in Pharmaceutical Development:
3-Formyl-4-nitrophenyl boronic acid pinacol ester is utilized as a key intermediate in the development of new pharmaceuticals. Its ability to form carbon-carbon bonds and create complex molecular structures makes it a valuable asset in the synthesis of potential drug candidates.
Used in Agrochemical Development:
Similarly, in the agrochemical industry, 3-Formyl-4-nitrophenyl boronic acid pinacol ester is employed as a building block for the synthesis of new agrochemicals. Its role in creating complex molecular structures contributes to the development of effective and targeted agrochemical products.
Used in Material Science:
3-Formyl-4-nitrophenyl boronic acid pinacol ester is also used in material science for the synthesis of advanced materials. Its ability to form carbon-carbon bonds and create complex structures is crucial for the development of new materials with unique properties and applications.

Upstream product

• 5551-12-2 4-bromo-2-nitrobenzaldehyde 
• 73183-34-3 bis(pinacol)diborane 
• 20357-20-4 5-bromo-2-nitrobenzaldehyde 

Downstream Products

• 1184264-91-2 N-[2-(3'-formyl-4'-nitro-biphenyl-2-yl)-ethyl]-benzenesulfonamide 

Relevant articles and documents

NOVEL 2-AMINO-QUINAZOLINE DERIVATIVES USEFUL AS INHIBITORS OF β-SECRETASE (BACE)

The present invention is directed to novel 2-amino-3,4-dihydro-quinazoline derivatives, pharmaceutical compositions containing them and their use in the treatment of Alzheimer’s disease (AD) and related disorders. The compounds of the invention are inhibitors of β-secretase, also known as β-site cleaving enzyme and BACE.

NOVEL 2-AMINO-QUINAZOLINE DERIVATIVES USEFUL AS INHIBITORS OF β-SECRETASE (BACE)

The present invention is directed to novel 2-amino-3, 4-dihydro-quinazoline derivatives, pharmaceutical compositions containing them and their use in the treatment of Alzheimer's disease (AD) and related disorders. The compounds of the invention are inhibitors of P-secretase, also known as n-site cleaving enzyme and BACE.

2-AMINO-QUINAZOLINE DERIVATIVES USEFUL AS INHIBITORS OF B-SECRETASE (BACE)

The present invention is directed to novel 2-amino-3,4-dihydro-quinazoline derivatives, pharmaceutical compositions containing them and their use in the treatment of Alzheimer's disease (AD) and related disorders. The compounds of the invention are inhibi