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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)-

3-Furanmethanamine, 2-methyl-

Cc1occc1CN Request for Quotation
Chemical Name: 3-Furanmethanamine, 2-methyl-
CAS Number: 35801-15-1
Product Number: AG00C8ML(AGN-PC-01XFVB)
Synonyms:
MDL No:
Molecular Formula: C6H9NO
Molecular Weight: 111.1418

Identification/Properties

Computed Properties
Molecular Weight:
111.144g/mol
XLogP3:
0.2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
111.068g/mol
Monoisotopic Mass:
111.068g/mol
Topological Polar Surface Area:
39.2A^2
Heavy Atom Count:
8
Formal Charge:
0
Complexity:
74.9
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


In chemical synthesis, (2-Methylfuran-3-yl)methanamine serves as a versatile building block with unique reactivity due to its furan ring and primary amine functional groups. This compound can participate in a variety of reactions to introduce the furan moiety or primary amine functionality into target molecules. (2-Methylfuran-3-yl)methanamine can be utilized in the preparation of pharmaceutical intermediates, agrochemicals, and functional materials by serving as a key intermediate in multistep synthesis routes. Its strategic placement within a molecular structure can influence the physicochemical properties and biological activities of the final compound. This compound is particularly valuable in the development of novel organic molecules with diverse applications in medicinal chemistry, materials science, and other fields.