Product Name:4-(tetramethyl-1,3,2-dioxaborolan-2-yl)-1h-indazole

IUPAC Name:4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indazole

Molecular Formula:C13H17BN2O2
Catalog Number:CM108910
Molecular Weight:244.1

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Product Details

CAS NO:885618-33-7
Molecular Formula:C13H17BN2O2
Melting Point:-
Smiles Code:CC1(C)OB(C2=CC=CC3=C2C=NN3)OC1(C)C
Catalog Number:CM108910
Molecular Weight:244.1
Boiling Point:
MDL No:MFCD08059267

Category Infos

Indazoles are a class of organic heterocyclic compounds, also known as 1,2-diazaindene and benzopyrazole. Indazole is a good bioisomer of phenol, which is more lipophilic than phenol and less prone to phase I and II metabolism. Indazole derivatives have a wide range of biological activities, and it has been confirmed that indazole compounds have anti-tumor, analgesic, anti-inflammatory and other drug activities. Anticancer is the most important application field of indazole drugs. Renal cell carcinoma, solid tumor, nausea and vomiting caused by chemotherapy and leukemia are the main indications of this structural backbone drug.
Boronic Acids and Esters
Boronic acids and boronate esters are commonly used reagents in Suzuki–Miyaura coupling chemistry. Organoboron derivatives are common reagents for C–C bond formation, either through classical palladium-mediated transformations or through other newer coupling methods. Boronic esters and acids are potential intermediates in the manufacture of many active pharmaceutical ingredients (API).
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Product Other Information

Product Overview 4-(Tetramethyl-1,3,2-dioxaborolan-2-yl)-1h-indazole (885618-33-7), with the chemical formula C13H17BN2O2, is an organic compound classified as an boronic esters. It contains a Indazole group attached to the boron.
Physical Properties Appearance: 4-(Tetramethyl-1,3,2-dioxaborolan-2-yl)-1h-indazole is a white to off-white solid.
Melting Point: When in solid form, it typically has a melting point between 139-142℃.
Chemical Properties 4-(Tetramethyl-1,3,2-dioxaborolan-2-yl)-1h-indazole a reactive compound, often utilized as a starting material or intermediate in various chemical reactions and synthesis processes. Additionally, it is non-toxic and has been often used in coupling reactions.
Synthesis and Application 4-(Tetramethyl-1,3,2-dioxaborolan-2-yl)-1h-indazole can be synthesized from a variety of precursors, including 1,3,2-dioxaborolane and 1H-indazole. This compound has been studied for its potential applications in various fields, including drug development, medicinal chemistry, and materials science. It has been shown to have a wide range of biochemical and physiological effects, as well as advantages and limitations for laboratory experiments.
Storage and Handling 4-(Tetramethyl-1,3,2-dioxaborolan-2-yl)-1h-indazole is also relatively stable and can be stored for long periods of time.