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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)-

4-Pyridinemethanamine, 3-methyl-

NCc1ccncc1C Request for Quotation
Chemical Name: 4-Pyridinemethanamine, 3-methyl-
CAS Number: 97004-05-2
Product Number: AG0065P1(AGN-PC-0K6A5J)
Synonyms:
MDL No:
Molecular Formula: C7H10N2
Molecular Weight: 122.1677

Identification/Properties

Properties
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
122.171g/mol
XLogP3:
0.1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
122.084g/mol
Monoisotopic Mass:
122.084g/mol
Topological Polar Surface Area:
38.9A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
83
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#:
2735
Hazard Statements:
H314
Precautionary Statements:
P280-P305+P351+P338-P310
Class:
8
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure


The (3-Methylpyridin-4-yl)methanamine compound plays a crucial role in chemical synthesis as a versatile building block. It serves as a valuable intermediate in the production of various pharmaceuticals, agrochemicals, and other fine chemicals. With its unique structure and reactivity, this compound can participate in a range of organic reactions, including coupling reactions, condensations, and functional group transformations. Its presence in the synthesis of heterocyclic compounds is particularly noteworthy, as it can facilitate the creation of complex molecular scaffolds with diverse properties. Additionally, (3-Methylpyridin-4-yl)methanamine can be utilized in the preparation of catalysts, polymers, and specialty materials, showcasing its significance in the realm of chemical research and development.