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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)-

3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)thiophene-2-carbonitrile

N#Cc1sccc1B1OC(C(O1)(C)C)(C)C Request for Quotation
Chemical Name: 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)thiophene-2-carbonitrile
CAS Number: 942070-34-0
Product Number: AG0065YH(AGN-PC-00QOL3)
Synonyms:
MDL No:
Molecular Formula: C11H14BNO2S
Molecular Weight: 235.1104

Identification/Properties

Properties
Storage:
2-8℃;
Computed Properties
Molecular Weight:
235.108g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
1
Exact Mass:
235.084g/mol
Monoisotopic Mass:
235.084g/mol
Topological Polar Surface Area:
70.5A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
320
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


The 3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)thiophene-2-carbonitrile compound is a versatile building block in chemical synthesis. It serves as a key reagent in the construction of complex organic molecules, particularly in the field of medicinal chemistry. This compound can be utilized in the formation of heterocyclic structures through Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of various pharmaceutical intermediates and bioactive compounds. Its unique structural features make it a valuable tool for the synthesis of novel organic materials with potential applications in drug discovery and material science. Additionally, the presence of the boronate moiety in this compound facilitates its involvement in diverse transformations, expanding its utility in the creation of functionalized organic molecules with tailored properties.