6-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indazole|937049-58-6,AngeneChemical

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Pyrimidine, 5-bromo-2-methyl-

1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide

2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-

O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]

Tris(dibenzylideneacetone)dipalladium

C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C

Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

6-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indazole

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Chemical Name:	6-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indazole
CAS Number:	937049-58-6
Product Number:	AG003EEE(AGN-PC-07135H)
Synonyms:
MDL No:
Molecular Formula:	C13H17BN2O2
Molecular Weight:	244.0973

Identification/Properties
Safety Information
NMR Spectrum
Other Analytical Data
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Identification/Properties

Properties

MP:

134-139°C

BP:

404.1°C at 760 mmHg

Storage:

Inert atmosphere;2-8℃;

Form:

Solid

Computed Properties

Molecular Weight:

244.101g/mol

Hydrogen Bond Donor Count:

Hydrogen Bond Acceptor Count:

Rotatable Bond Count:

Exact Mass:

244.138g/mol

Monoisotopic Mass:

244.138g/mol

Topological Polar Surface Area:

47.1A^2

Heavy Atom Count:

Formal Charge:

Complexity:

319

Isotope Atom Count:

Defined Atom Stereocenter Count:

Undefined Atom Stereocenter Count:

Defined Bond Stereocenter Count:

Undefined Bond Stereocenter Count:

Covalently-Bonded Unit Count:

Compound Is Canonicalized:

Yes

Safety Information

GHS Pictogram:

Signal Word:

Warning

UN#:

N/A

Hazard Statements:

H302-H315-H319-H335

Precautionary Statements:

P261-P305+P351+P338

Class:

N/A

Packing Group:

N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure

1H-Indazole-6-boronic acid pinacol ester is a versatile compound widely utilized in chemical synthesis as a valuable building block. This specific boronic acid derivative has found significant application in the development and synthesis of pharmaceuticals, agrochemicals, and materials due to its unique reactivity and compatibility with a variety of coupling reactions.In organic synthesis, 1H-Indazole-6-boronic acid pinacol ester serves as an important intermediate for the preparation of complex molecules through cross-coupling reactions such as Suzuki-Miyaura coupling, Stille coupling, and Sonogashira coupling. By incorporating this compound into the synthetic pathway, chemists can introduce the indazole group with precision, allowing for the synthesis of structurally diverse compounds with specific biological or chemical properties.Furthermore, the pinacol ester functionality of this compound plays a crucial role in enhancing its stability and facilitating its manipulation in various synthetic processes. The presence of the boronic acid moiety provides a handle for further functionalization, enabling the incorporation of additional substituents or the formation of new bonds, thereby expanding the structural diversity and complexity of the final products.Overall, the strategic incorporation of 1H-Indazole-6-boronic acid pinacol ester in chemical synthesis enables researchers to access novel compounds with tailored properties and functionalities, making it a valuable tool in the development of innovative molecules for a wide range of applications.