1. Home
  2. Quinoline, 6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-

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)-

Quinoline, 6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-

CC1(C)OB(OC1(C)C)c1ccc2c(c1)cccn2 Request for Quotation
Chemical Name: Quinoline, 6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-
CAS Number: 406463-06-7
Product Number: AG00769S(AGN-PC-00UQMN)
Synonyms:
MDL No:
Molecular Formula: C15H18BNO2
Molecular Weight: 255.1199

Identification/Properties

Computed Properties
Molecular Weight:
255.124g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
255.143g/mol
Monoisotopic Mass:
255.143g/mol
Topological Polar Surface Area:
31.4A^2
Heavy Atom Count:
19
Formal Charge:
0
Complexity:
329
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
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

Request for Quotation

Customer Feedback

Chemical Structure


6-Quinolineboronic acid pinacol ester is a versatile compound used in chemical synthesis for its ability to act as a boronic acid derivative. This compound is commonly employed as a key building block in the synthesis of various biologically active molecules and pharmaceuticals. Its unique structure consisting of a quinoline core and boronic acid functionality makes it a valuable tool in organic chemistry.In chemical synthesis, 6-Quinolineboronic acid pinacol ester serves as a potent reagent for Suzuki-Miyaura cross-coupling reactions, enabling the formation of complex carbon-carbon bonds. This reaction is widely utilized in the pharmaceutical industry for the construction of drug candidates and other bioactive compounds. Additionally, this compound can also participate in other cross-coupling reactions such as Sonogashira and Heck reactions, further expanding its synthetic utility.Furthermore, 6-Quinolineboronic acid pinacol ester has been instrumental in the development of novel materials and catalysts due to its versatile reactivity and compatibility with various reaction conditions. Its incorporation into molecular frameworks has led to the generation of new compounds with diverse properties and applications in materials science.Overall, the unique characteristics and reactivity of 6-Quinolineboronic acid pinacol ester make it an essential tool in chemical synthesis, enabling the efficient construction of complex molecules with potential pharmaceutical and material applications.