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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-(aminomethyl)oxan-4-yl]methanol

NCC1(CO)CCOCC1 Request for Quotation
Chemical Name: [4-(aminomethyl)oxan-4-yl]methanol
CAS Number: 959238-22-3
Product Number: AG00IJJ7(AGN-PC-03OHVP)
Synonyms:
MDL No:
Molecular Formula: C7H15NO2
Molecular Weight: 145.1995

Identification/Properties

Computed Properties
Molecular Weight:
145.202g/mol
XLogP3:
-0.9
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
145.11g/mol
Monoisotopic Mass:
145.11g/mol
Topological Polar Surface Area:
55.5A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
99.8
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The compound 4-(Aminomethyl)tetrahydro-2H-pyran-4-yl)methanol, also known as $name$, plays a crucial role in chemical synthesis as a versatile building block. Its unique structural properties make it a valuable intermediate in the creation of a wide range of complex organic molecules. By incorporating $name$ into various synthetic pathways, chemists can access novel structures with diverse functionalities.One of the key applications of $name$ is in the synthesis of heterocyclic compounds. The presence of both an amine and a hydroxyl group in its structure allows for efficient derivatization and functionalization. Chemists can utilize these reactive sites to introduce additional substituents or form various chemical bonds, expanding the scope of possible synthetic routes.Moreover, the tetrahydro-2H-pyran moiety in $name$ confers unique reactivity and stereochemistry to the synthesized molecules. This structural motif can participate in various ring-closing reactions, leading to the formation of cyclic compounds with specific spatial arrangements. Additionally, the presence of the aminomethyl group enhances the nucleophilicity of the molecule, enabling it to participate in a wide range of transformations, such as reductive amination or imine formation.Overall, the strategic incorporation of (4-(Aminomethyl)tetrahydro-2H-pyran-4-yl)methanol in chemical synthesis allows for the efficient construction of structurally complex and diverse organic molecules with potential applications in drug discovery, material science, and agrochemical research.