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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, 2-(3-hexyl-2-thienyl)-4,4,5,5-tetramethyl-

CCCCCCc1ccsc1B1OC(C(O1)(C)C)(C)C Request for Quotation
Chemical Name: 1,3,2-Dioxaborolane, 2-(3-hexyl-2-thienyl)-4,4,5,5-tetramethyl-
CAS Number: 850881-09-3
Product Number: AG003JIP(AGN-PC-0146AF)
Synonyms:
MDL No:
Molecular Formula: C16H27BO2S
Molecular Weight: 294.2604

Identification/Properties

Properties
BP:
385.3 °C at 760 mmHg
Storage:
Room Temperature;Light sensitive;Inert atmosphere;
Form:
Liquid
Computed Properties
Molecular Weight:
294.26g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
6
Exact Mass:
294.182g/mol
Monoisotopic Mass:
294.182g/mol
Topological Polar Surface Area:
46.7A^2
Heavy Atom Count:
20
Formal Charge:
0
Complexity:
304
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-(3-Hexylthiophen-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is a versatile chemical compound widely used in organic synthesis processes. This boron-containing compound serves as an important building block in the preparation of various functional molecules due to its unique properties.One significant application of 2-(3-Hexylthiophen-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is in Suzuki-Miyaura cross-coupling reactions. This compound acts as a key component in this widely employed organic transformation, facilitating the coupling of aryl or vinyl halides with boronic acids or boronates. The resulting products are valuable intermediates in the synthesis of pharmaceuticals, agrochemicals, polymers, and materials.Furthermore, 2-(3-Hexylthiophen-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane exhibits good stability and compatibility with a variety of reaction conditions, making it a preferred choice for chemists seeking efficient and selective bond-forming strategies. Its incorporation in chemical synthesis processes enables the rapid construction of complex molecular architectures with high efficiency and control.Overall, the utility of 2-(3-Hexylthiophen-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane in chemical synthesis highlights its significance as a key reagent for the construction of diverse organic compounds with wide-ranging applications.