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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)-

tert-butyl N-[3-bromo-1-(oxan-4-yl)propyl]carbamate

BrCCC(C1CCOCC1)NC(=O)OC(C)(C)C Request for Quotation
Chemical Name: tert-butyl N-[3-bromo-1-(oxan-4-yl)propyl]carbamate
CAS Number: 924817-72-1
Product Number: AG00654O(AGN-PC-04Q6NR)
Synonyms:
MDL No: MFCD06410600
Molecular Formula: C13H24BrNO3
Molecular Weight: 322.2386

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Chemical Structure


The tert-Butyl (3-bromo-1-(tetrahydro-2H-pyran-4-yl)propyl)carbamate is a versatile compound commonly used in chemical synthesis processes. This compound's strategic use lies in its ability to function as a selective protecting group for amines, particularly in complex organic molecule synthesis. By employing this tert-Butyl (3-bromo-1-(tetrahydro-2H-pyran-4-yl)propyl)carbamate, chemists can shield specific amine functional groups within a molecule, allowing for selective manipulation of other reactive sites without affecting the protected amines. This protective action ensures that the desired chemical transformations occur selectively at designated positions, enabling precise control over the synthetic pathway toward the target compound.