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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-(Boc-Aminomethyl)-3-amino-oxolane

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Chemical Name: 3-(Boc-Aminomethyl)-3-amino-oxolane
CAS Number: 1158760-39-4
Product Number: AG00HD42(AGN-PC-0WCKIV)
Synonyms:
MDL No: MFCD12408620
Molecular Formula:
Molecular Weight:

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Chemical Structure


3-(Boc-Aminomethyl)-3-aminooxolane is a versatile compound commonly used in chemical synthesis due to its unique structure and reactivity. The Boc (tert-butoxycarbonyl) group serves as a protecting group for the amino functionality, allowing for selective manipulation of the molecule during various synthetic transformations. This compound is particularly valuable in the field of medicinal chemistry for the introduction of amino groups in a controlled manner, essential for the synthesis of pharmaceuticals and bioactive molecules. Additionally, the oxolane ring provides structural diversity and rigidity, making it an important building block for the creation of novel compounds with enhanced biological properties. Furthermore, the presence of both amine and Boc-protected amine functionalities offers opportunities for the construction of complex molecules through solid-phase synthesis or solution-phase chemistry.