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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-methyl-2-(oxolan-3-ylmethoxy)phenyl]methanamine

NCc1ccc(cc1OCC1COCC1)C Request for Quotation
Chemical Name: [4-methyl-2-(oxolan-3-ylmethoxy)phenyl]methanamine
CAS Number: 1250057-67-0
Product Number: AG019Z59(AG019Z59)
Synonyms:
MDL No:
Molecular Formula: C13H19NO2
Molecular Weight: 221.2955

Identification/Properties

Computed Properties
Molecular Weight:
221.3g/mol
XLogP3:
1.4
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
4
Exact Mass:
221.142g/mol
Monoisotopic Mass:
221.142g/mol
Topological Polar Surface Area:
44.5A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
210
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
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 compound [4-methyl-2-(oxolan-3-ylmethoxy)phenyl]methanamine, also known as $name$, is a versatile building block in chemical synthesis. It is commonly used as a key intermediate in the preparation of various pharmaceutical compounds due to its structural versatility and functional groups that can be modified to enhance desired properties. In chemical synthesis, $name$ serves as a valuable starting material for the construction of complex molecules and drug candidates through various synthetic routes. Its unique structure enables the introduction of different substituents and modifications, providing a platform for the creation of novel chemical entities with potential pharmacological activities. Furthermore, the presence of the oxolane ring contributes to the compound's stability and reactivity, making it a useful tool in the synthesis of biologically active molecules.