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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)-

lithium;trihydroxy(pyridin-2-yl)boranuide

O[B-](c1ccccn1)(O)O.[Li+] Request for Quotation
Chemical Name: lithium;trihydroxy(pyridin-2-yl)boranuide
CAS Number: 1393822-96-2
Product Number: AG001AW6(AGN-PC-0BLDA6)
Synonyms:
MDL No:
Molecular Formula: C5H7BLiNO3
Molecular Weight: 146.8660

Identification/Properties

Computed Properties
Molecular Weight:
146.865g/mol
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
0
Exact Mass:
147.068g/mol
Monoisotopic Mass:
147.068g/mol
Topological Polar Surface Area:
73.6A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
119
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:
2
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


Lithium trihydroxy(pyridin-2-yl)borate, also known as LiTPyB, is a versatile compound widely used in chemical synthesis as a highly efficient and selective catalyst. Its unique structure allows it to facilitate a variety of reactions with precision and control, making it a valuable tool for synthetic chemists.In organic synthesis, LiTPyB is commonly used in cross-coupling reactions to form carbon-carbon or carbon-heteroatom bonds. Its ability to activate aryl halides and other electrophiles enables the formation of complex molecular structures with high efficiency. Additionally, LiTPyB plays a crucial role in the activation of challenging substrates, such as hindered or deactivated aryl halides, leading to enhanced reactivity and selectivity in various transformations.Moreover, LiTPyB has found applications in the functionalization of aromatic compounds, the preparation of organoboronic acids, and the synthesis of heterocyclic compounds. Its compatibility with a wide range of functional groups and reaction conditions further expands its utility in diverse synthetic methodologies.Overall, Lithium trihydroxy(pyridin-2-yl)borate stands out as a versatile and effective catalyst in chemical synthesis, facilitating the creation of complex molecular architectures with remarkable precision and efficiency.