1. Home
  2. 1-propyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrazole

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
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)-

1-propyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrazole

CCCn1ccc(n1)B1OC(C(O1)(C)C)(C)C Request for Quotation
Chemical Name: 1-propyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrazole
CAS Number: 934586-51-3
Product Number: AG0062LY(AGN-PC-0GX66H)
Synonyms:
MDL No:
Molecular Formula: C12H21BN2O2
Molecular Weight: 236.1183

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;

Safety Information

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


1-Propyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole is a versatile compound widely utilized in chemical synthesis processes. This compound serves as a crucial building block in the creation of complex organic molecules with diverse applications. Its unique structural properties and reactivity make it ideal for use in various transformations and reactions.In chemical synthesis, 1-Propyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole is commonly employed as a ligand in metal-catalyzed cross-coupling reactions. This compound plays a pivotal role in facilitating the formation of carbon-carbon bonds, essential for the construction of elaborate molecular structures. Additionally, it can act as a stabilizing agent for reactive intermediates, enhancing the efficiency and selectivity of synthetic processes.Moreover, the incorporation of 1-Propyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole in chemical transformations enables the precise modification of functional groups, enabling chemists to tailor the properties of target molecules for specific applications. Its versatility and compatibility with a wide range of substrates make it a valuable tool in organic synthesis, driving innovation and advancement in the field of chemistry.