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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)-

(3R,4R)-1-(tert-Butoxycarbonyl)-4-(4-fluorophenyl)piperidine-3-carboxylic acid

OC(=O)[C@H]1CN(CC[C@H]1c1ccc(cc1)F)C(=O)OC(C)(C)C Request for Quotation
Chemical Name: (3R,4R)-1-(tert-Butoxycarbonyl)-4-(4-fluorophenyl)piperidine-3-carboxylic acid
CAS Number: 951167-03-6
Product Number: AG0066HJ(AGN-PC-0WAHU9)
Synonyms:
MDL No:
Molecular Formula: C17H22FNO4
Molecular Weight: 323.3593

Identification/Properties

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


The (3R,4R)-1-(tert-Butoxycarbonyl)-4-(4-fluorophenyl)piperidine-3-carboxylic acid is a highly versatile compound that finds widespread applications in chemical synthesis. This compound serves as a key building block in the creation of various pharmaceuticals, agrochemicals, and fine chemicals due to its unique structural features and reactivity.In chemical synthesis, (3R,4R)-1-(tert-Butoxycarbonyl)-4-(4-fluorophenyl)piperidine-3-carboxylic acid acts as a crucial intermediate for the preparation of complex organic molecules. Its functional groups and stereochemistry make it an ideal candidate for the formation of diverse chemical bonds and structural motifs. By utilizing this compound, chemists can efficiently access a wide range of target molecules with specific biological or chemical properties.Moreover, the presence of the tert-Butoxycarbonyl (Boc) protecting group in the structure of this compound enables selective reactions at other reactive sites without affecting the desired functionality. This protective group strategy plays a vital role in controlling the sequence and outcome of chemical transformations during synthesis, leading to higher yields and purities of the final products.Overall, the application of (3R,4R)-1-(tert-Butoxycarbonyl)-4-(4-fluorophenyl)piperidine-3-carboxylic acid in chemical synthesis offers chemists a powerful tool to access complex molecules efficiently and reliably, making it indispensable in modern organic chemistry research and drug discovery efforts.