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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-methoxypyrimidin-5-yl)methanamine

COc1ncc(cn1)CN Request for Quotation
Chemical Name: (2-methoxypyrimidin-5-yl)methanamine
CAS Number: 944899-18-7
Product Number: AG00II8G(AGN-PC-0ALJBE)
Synonyms:
MDL No:
Molecular Formula: C6H9N3O
Molecular Weight: 139.15516

Identification/Properties

Computed Properties
Molecular Weight:
139.158g/mol
XLogP3:
-0.6
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
139.075g/mol
Monoisotopic Mass:
139.075g/mol
Topological Polar Surface Area:
61A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
91
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:
Danger
UN#:
2811
Hazard Statements:
H301
Precautionary Statements:
P301+P310
Class:
6.1
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure


The compound (2-Methoxypyrimidin-5-yl)methanamine, also known as $name$, plays a pivotal role in chemical synthesis due to its versatile applications. As a key building block in organic chemistry, $name$ serves as a valuable intermediate in the production of various pharmaceuticals, agrochemicals, and specialty chemicals. Its unique structure and reactivity make it an essential component in the synthesis of complex molecules, including heterocyclic compounds and biologically active substances. By serving as a nucleophilic amine, $name$ can participate in a range of synthetic transformations such as nucleophilic substitution, reductive amination, and Suzuki-Miyaura coupling reactions. Its ability to functionalize aromatic rings and form stable amide linkages expands its utility in the creation of diverse chemical entities with tailored properties. In summary, the use of (2-Methoxypyrimidin-5-yl)methanamine in chemical synthesis enables the efficient construction of intricate molecular structures and opens up new avenues for innovation in the field of organic chemistry.