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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)-

(6-cyclobutyloxypyridin-3-yl)methanamine

NCc1ccc(nc1)OC1CCC1 Request for Quotation
Chemical Name: (6-cyclobutyloxypyridin-3-yl)methanamine
CAS Number: 1247205-52-2
Product Number: AG000MNY(AGN-PC-0EEQ2Y)
Synonyms:
MDL No:
Molecular Formula: C10H14N2O
Molecular Weight: 178.2310

Identification/Properties

Computed Properties
Molecular Weight:
178.235g/mol
XLogP3:
0.9
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
178.111g/mol
Monoisotopic Mass:
178.111g/mol
Topological Polar Surface Area:
48.1A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
159
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


The application of (6-Cyclobutoxypyridin-3-yl)methanamine in chemical synthesis lies in its versatile capabilities as a building block for the creation of complex organic molecules. This compound serves as a crucial intermediate in the synthesis of various pharmaceuticals, agrochemicals, and specialty chemicals. Its unique structural properties make it a valuable tool for chemists in designing and constructing novel molecular structures with specific functionalities. By utilizing (6-Cyclobutoxypyridin-3-yl)methanamine in chemical reactions, researchers can access a diverse array of potential products, opening up possibilities for the development of new materials and compounds in the field of organic chemistry. This compound's importance in synthesis lies in its ability to facilitate the production of advanced chemical compounds with tailored properties, making it an indispensable component in the toolkit of synthetic chemists.