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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)-

N-methyl-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)quinazolin-2-amine

CNc1ncc2c(n1)ccc(c2)B1OC(C(O1)(C)C)(C)C Request for Quotation
Chemical Name: N-methyl-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)quinazolin-2-amine
CAS Number: 913067-91-1
Product Number: AG006OUC(AGN-PC-00SRBB)
Synonyms:
MDL No:
Molecular Formula: C15H20BN3O2
Molecular Weight: 285.1492

Identification/Properties

Properties
BP:
450.1 °C at 760 mmHg
Storage:
Light sensitive;Keep in dry area;2-8℃;
Computed Properties
Molecular Weight:
285.154g/mol
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
2
Exact Mass:
285.165g/mol
Monoisotopic Mass:
285.165g/mol
Topological Polar Surface Area:
56.3A^2
Heavy Atom Count:
21
Formal Charge:
0
Complexity:
375
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:
H302-H315-H319-H332-H335
Precautionary Statements:
P280-P305+P351+P338-P310
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


N-Methyl-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)quinazolin-2-amine is a versatile compound commonly used in chemical synthesis. This compound is especially valuable in organic chemistry due to its ability to act as a key building block in the creation of various pharmaceuticals, agrochemicals, and materials.The presence of the N-methyl group in this compound enhances its reactivity and allows for efficient functional group transformations in the synthesis of complex molecules. Furthermore, the boron-containing moiety in the structure facilitates Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in a controlled and effective manner.Overall, the application of N-Methyl-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)quinazolin-2-amine in chemical synthesis plays a crucial role in the development of diverse chemical compounds with important industrial and pharmaceutical applications.