1040424-52-9

Usage

Uses

Used in Pharmaceutical Industry:
4'-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-[1,1'-biphenyl]-4-carbaldehyde is used as a key intermediate in the synthesis of pharmaceutical compounds due to its ability to facilitate the formation of complex molecular structures. Its unique boron-containing framework enhances the efficiency of organic reactions, contributing to the development of novel drugs with improved therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical sector, 4'-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-[1,1'-biphenyl]-4-carbaldehyde is utilized as a vital component in the production of various agrochemicals. Its role in organic synthesis allows for the creation of molecules with specific pesticidal or herbicidal properties, thereby contributing to the development of effective crop protection agents.
Used in Organic Chemistry Research:
4'-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-[1,1'-biphenyl]-4-carbaldehyde is employed as a versatile tool in organic chemistry research for exploring new reaction pathways and developing innovative synthetic methods. Its reactivity and structural features make it an ideal candidate for studying the mechanisms of carbon-carbon bond formation and other related chemical processes.
Overall, 4'-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-[1,1'-biphenyl]-4-carbaldehyde's diverse applications highlight its significance in the fields of pharmaceuticals, agrochemicals, and organic chemistry research, where it plays a crucial role in the synthesis of complex organic molecules and the advancement of novel chemical reactions.

Upstream product

• 87199-17-5 4-formylphenylboronic acid, 
• 589-87-7 1,4-bromoiodobenzene 
• 50670-58-1 4-formyl-4'-bromobiphenyl 
• 73183-34-3 bis(pinacol)diborane 

Downstream Products

• 1040424-59-6 C₈₄H₈₆O₆ 

Relevant academic research and scientific papers

Aminal-Linked Covalent Organic Frameworks through Condensation of Secondary Amine with Aldehyde

New linkage chemistry will endow covalent organic frameworks (COFs) with not only structural diversity but also fascinating properties. However, to develop a new type of linkages has been a great challenge. We herein report the first two COFs using aminal

Multifunctional photoresponsive organic molecule for electric field sensing and modulation

Nonlinear optical organic molecules have advanced a wide range of fields spanning from integrated photonics to biological imaging. With advances in molecular design, an emerging application is multifunctional nonlinear organic materials. Unlike conventional molecules which simply emit light through single or multi photon processes, multifunctional materials can perform multiple tasks, such as modulating the optical signal or reporting an electric field intensity. In this work, we report a multifunctional organic molecular device with electric field 'sense-and-modulate' capability. This is achieved by combining two distinct functional modules. The electric field-reporting module relies on a photo-induced electron transfer (PeT) dye, tetraphenylethylene (TPE) as a two-photon (2p) imaging agent; while the electric field-modulating module relies on the organic photoconductor, naphthalimide (NAI). To reduce cross-talk between the two modules, they are separated by a long alkyl chain. The photophysical properties and photoconductivity of the probe molecule are studied in a range of solvents and in the solid state, and the results agree with the density functional theory predictions. Specifically, 2p excitation is demonstrated, and the photoconductivity is rapid and reversible. The entire system is optically controlled, including signal read-out, and the two modules can be operated simultaneously or individually.

AMPK ACTIVATORS

This disclosure is directed, at least in part, to AMPK activators useful for the treatment of conditions or disorders associated with AMPK. In some embodiments, the condition or disorder is associated with the gut-brain axis. In some embodiments, condition or disorder is associated with systemic infection and inflammation from having a leaky gut barrier. In some embodiments, the AMPK activators are gut-restricted compounds. In some embodiments, the AMPK activators are agonists, super agonists, full agonists, or partial agonists.

Unsaturated strained cyclophanes based on dibenz[a,j]anthracene by an intramolecular McMurry olefination

(Chemical Equation Presented) A new type of rigid conjugated unsaturated strained cyclophane derivative containing dibenz[a,j]anthracene units was facilely synthesized through an intramolecular McMurry reaction without intermolecular dimerization products