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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, 4,4,5,5-tetramethyl-2-[4-(methylthio)phenyl]-

CSc1ccc(cc1)B1OC(C(O1)(C)C)(C)C Request for Quotation
Chemical Name: 1,3,2-Dioxaborolane, 4,4,5,5-tetramethyl-2-[4-(methylthio)phenyl]-
CAS Number: 190788-58-0
Product Number: AG002ET0(AGN-PC-01LR28)
Synonyms:
MDL No:
Molecular Formula: C13H19BO2S
Molecular Weight: 250.1648

Identification/Properties

Properties
MP:
35.1-35.9℃
BP:
344.5°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
250.163g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
250.12g/mol
Monoisotopic Mass:
250.12g/mol
Topological Polar Surface Area:
43.8A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
257
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-H413
Precautionary Statements:
P264-P270-P273-P301+P312-P330
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


4,4,5,5-Tetramethyl-2-(4-(methylthio)phenyl)-1,3,2-dioxaborolane, also known as $name$, is a versatile chemical compound commonly utilized in various chemical synthesis processes. This compound plays a crucial role as a boron-containing building block in organic chemistry. Its unique structure confers it with valuable properties that enable its application in a range of synthetic strategies.One primary application of $name$ in chemical synthesis is as a key reagent in Suzuki-Miyaura cross-coupling reactions. In this widely used reaction, $name$ acts as a boronate ester, facilitating the coupling of aryl halides or pseudohalides with organoboron species under mild conditions. This reaction allows for the efficient formation of carbon-carbon bonds, enabling the construction of complex organic molecules with high selectivity and efficacy.Furthermore, $name$ can also serve as a valuable precursor in the synthesis of biaryl compounds, which are essential structural motifs found in many pharmaceuticals, agrochemicals, and materials. Through its participation in diverse synthetic transformations, $name$ contributes to the development of novel organic compounds with desired properties and functionalities.Overall, the application of 4,4,5,5-Tetramethyl-2-(4-(methylthio)phenyl)-1,3,2-dioxaborolane in chemical synthesis underscores its significance as a versatile building block with diversified utility in the creation of intricate molecular structures and the advancement of organic synthesis methodologies.