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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)-

(6-ethylsulfanylpyridin-3-yl)boronic acid

CCSc1ccc(cn1)B(O)O Request for Quotation
Chemical Name: (6-ethylsulfanylpyridin-3-yl)boronic acid
CAS Number: 1217501-38-6
Product Number: AG0015S3(AGN-PC-09PYY3)
Synonyms:
MDL No:
Molecular Formula: C7H10BNO2S
Molecular Weight: 183.0358

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Computed Properties
Molecular Weight:
183.032g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
Exact Mass:
183.053g/mol
Monoisotopic Mass:
183.053g/mol
Topological Polar Surface Area:
78.6A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
137
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:
H317-H319
Precautionary Statements:
P305+P351+P338-P280
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


(6-(Ethylthio)pyridin-3-yl)boronic acid is a versatile reagent widely used in chemical synthesis as a key building block and cross-coupling agent. This compound is valued for its ability to participate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of biaryl compounds through the coupling of aryl halides with aryl boronic acids. Additionally, (6-(Ethylthio)pyridin-3-yl)boronic acid can be employed in the synthesis of pharmaceuticals, agrochemicals, and materials science, where the pyridine ring serves as a valuable heterocyclic scaffold for introducing functionality and enhancing molecular properties. The ethylthio substituent further expands the synthetic versatility of this compound, allowing for the selective modification of pyridine-based molecules. Overall, (6-(Ethylthio)pyridin-3-yl)boronic acid is a crucial tool in the arsenal of synthetic chemists for constructing complex organic molecules with precision and efficiency.