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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)-

(R)-tert-Butyl (6-oxopiperidin-3-yl)carbamate

O=C1CC[C@H](CN1)NC(=O)OC(C)(C)C Request for Quotation
Chemical Name: (R)-tert-Butyl (6-oxopiperidin-3-yl)carbamate
CAS Number: 1228566-94-6
Product Number: AG000JM9(AGN-PC-0WAGHF)
Synonyms:
MDL No:
Molecular Formula: C10H18N2O3
Molecular Weight: 214.2615

Identification/Properties

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302
Precautionary Statements:
P280-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


(R)-tert-Butyl (6-oxopiperidin-3-yl)carbamate, also known as $name$, is a versatile compound widely used in chemical synthesis. Its unique chemical structure makes it a valuable building block in the preparation of various organic molecules. In particular, (R)-tert-Butyl (6-oxopiperidin-3-yl)carbamate is commonly employed in the synthesis of pharmaceutical intermediates, agrochemicals, and specialty chemicals.One of the key applications of (R)-tert-Butyl (6-oxopiperidin-3-yl)carbamate is in asymmetric synthesis, where its chiral nature allows for the creation of enantiopure compounds. This is crucial in the pharmaceutical industry, where the chirality of a molecule can significantly impact its biological activity and pharmacological properties. By utilizing (R)-tert-Butyl (6-oxopiperidin-3-yl)carbamate as a starting material, chemists can access a wide range of chiral compounds with high enantiomeric purity.Furthermore, (R)-tert-Butyl (6-oxopiperidin-3-yl)carbamate serves as a masked amine functionality, enabling the selective introduction of amines into target molecules. This is especially important in the construction of complex organic molecules, allowing chemists to control the timing and regiochemistry of amine incorporation.Overall, the use of (R)-tert-Butyl (6-oxopiperidin-3-yl)carbamate in chemical synthesis offers a powerful tool for the efficient and selective preparation of chiral compounds and structurally diverse molecules. Its versatility and utility make it an invaluable component in the toolbox of synthetic chemists aiming to access new and challenging chemical structures.