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  2. 2-amino-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine-4-carbonitrile

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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)-

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

N#Cc1cc(N)ncc1B1OC(C(O1)(C)C)(C)C Request for Quotation
Chemical Name: 2-amino-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine-4-carbonitrile
CAS Number: 944401-73-4
Product Number: AG00II6A(AGN-PC-0CYRQI)
Synonyms:
MDL No:
Molecular Formula: C12H16BN3O2
Molecular Weight: 245.0853

Identification/Properties

Computed Properties
Molecular Weight:
245.089g/mol
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
1
Exact Mass:
245.134g/mol
Monoisotopic Mass:
245.134g/mol
Topological Polar Surface Area:
81.2A^2
Heavy Atom Count:
18
Formal Charge:
0
Complexity:
361
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-Amino-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)isonicotinonitrile is a versatile compound widely utilized in chemical synthesis for its unique properties and reactivity. This compound serves as a crucial building block in various organic reactions and plays a significant role in the creation of complex molecules.In chemical synthesis, 2-Amino-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)isonicotinonitrile acts as a key intermediate in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals. Its functional groups enable it to participate in a range of important reactions, such as Suzuki coupling, cross-coupling reactions, and palladium-catalyzed transformations.Furthermore, the presence of the boronic ester moiety in this compound allows for selective functionalization and modification, making it a valuable tool in designing and constructing complex organic molecules with high precision and efficiency. Its use in chemical synthesis has led to the development of innovative synthetic routes and methodologies, facilitating the access to diverse molecular structures with potential applications across various fields of chemistry.