1. Home
  2. 1,3,2-Dioxaborolane, 4,4,5,5-tetramethyl-2-(1-phenylethenyl)-

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)-

1,3,2-Dioxaborolane, 4,4,5,5-tetramethyl-2-(1-phenylethenyl)-

C=C(c1ccccc1)B1OC(C(O1)(C)C)(C)C Request for Quotation
Chemical Name: 1,3,2-Dioxaborolane, 4,4,5,5-tetramethyl-2-(1-phenylethenyl)-
CAS Number: 143825-84-7
Product Number: AG001IFI(AGN-PC-0NEQS6)
Synonyms:
MDL No:
Molecular Formula: C14H19BO2
Molecular Weight: 230.1105

Identification/Properties

Properties
MP:
42-49 °C
BP:
277.3°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
230.114g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
230.148g/mol
Monoisotopic Mass:
230.148g/mol
Topological Polar Surface Area:
18.5A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
287
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#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


4,4,5,5-Tetramethyl-2-(1-phenylvinyl)-1,3,2-dioxaborolane is a versatile compound widely used in chemical synthesis as a cross-coupling reagent. This compound plays a crucial role in the formation of carbon-carbon bonds through palladium-catalyzed coupling reactions. It is particularly useful in the synthesis of pharmaceuticals, agrochemicals, and advanced materials.Its unique structure allows for efficient and selective couplings, leading to the formation of complex molecules with high precision. The presence of boron in its structure enhances the reactivity and stability of the intermediate species, making it a preferred choice in modern organic synthesis strategies.Moreover, 4,4,5,5-Tetramethyl-2-(1-phenylvinyl)-1,3,2-dioxaborolane offers excellent functional group compatibility and can be easily modified to suit specific synthetic needs. Its application extends to the construction of challenging molecular architectures and the development of novel chemical entities with diverse applications.Overall, this compound is a valuable tool in the hands of synthetic chemists, enabling the efficient construction of complex molecules and facilitating the discovery of new compounds with potential therapeutic, agricultural, and material science applications.