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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-Cyanopyridine-2-boronic Acid Pinacol Ester

N#Cc1cccc(n1)B1OC(C(O1)(C)C)(C)C Request for Quotation
Chemical Name: 6-Cyanopyridine-2-boronic Acid Pinacol Ester
CAS Number: 952402-79-8
Product Number: AG003N76(AGN-PC-0WAFT8)
Synonyms:
MDL No:
Molecular Formula: C12H15BN2O2
Molecular Weight: 230.0707

Identification/Properties

Properties
BP:
365.6°C at 760 mmHg
Storage:
Inert atmosphere;-10 ℃;
Form:
Solid
Computed Properties
Molecular Weight:
230.074g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
1
Exact Mass:
230.123g/mol
Monoisotopic Mass:
230.123g/mol
Topological Polar Surface Area:
55.1A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
332
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
Precautionary Statements:
P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


6-Cyanopyridine-2-boronic acid pinacol ester, also known as $name$, serves as a versatile building block in organic synthesis. This compound is commonly utilized as a key reagent in the preparation of various biologically active molecules and pharmaceutical intermediates. Through its boronic acid functionality, $name$ plays a crucial role in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds. This precise and efficient method is essential in the synthesis of complex organic compounds for drug discovery and medicinal chemistry research. Additionally, the cyano group in 6-Cyanopyridine-2-boronic acid pinacol ester offers a valuable handle for further elaboration, allowing chemists to introduce a wide range of functional groups and structural modifications. As a result, $name$ is an indispensable tool for synthetic chemists seeking to access novel chemical entities with potential therapeutic applications.