1. Home
  2. 3-[3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]pyridine

Contact Angene

Tel: +852 8191 6999

Email: sales@angenechemical.com

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)-

3-[3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]pyridine

CC1(C)OB(OC1(C)C)c1cccc(c1)c1cccnc1 Request for Quotation
Chemical Name: 3-[3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]pyridine
CAS Number: 939430-30-5
Product Number: AG00IHVT(AGN-PC-0WAMFG)
Synonyms:
MDL No: MFCD20923943
Molecular Formula: C17H20BNO2
Molecular Weight: 281.1572

Identification/Properties

Computed Properties
Molecular Weight:
281.162g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
281.159g/mol
Monoisotopic Mass:
281.159g/mol
Topological Polar Surface Area:
31.4A^2
Heavy Atom Count:
21
Formal Charge:
0
Complexity:
356
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-H412
Precautionary Statements:
P273-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


3-[3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]pyridine, commonly known as $name$, is a versatile compound widely used in chemical synthesis. This compound plays a crucial role as a key building block in the field of organic chemistry, particularly in the synthesis of complex molecules. Its unique structure enables it to participate in various reactions, making it a valuable tool for chemists in designing and creating new compounds. In chemical synthesis, $name$ is often employed as a reagent for Suzuki-Miyaura cross-coupling reactions, where it serves as a coupling partner alongside aryl halides or pseudohalides to form biaryl compounds. Additionally, $name$ can also be utilized in transition metal-catalyzed C-H activation reactions and other transformations that require the introduction of functional groups at specific positions on aromatic rings. Furthermore, its compatibility with a wide range of reaction conditions and its ability to facilitate selective bond formations make $name$ an indispensable component in the toolbox of synthetic chemists.