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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(1R,3S,4S)-3-(6-bromo-1H-benzimidazol-2-yl)-2-azabicyclo[2.2.1]heptane-2-carboxylate (GS-459990)

Brc1ccc2c(c1)[nH]c(n2)[C@@H]1[C@H]2CC[C@@H](N1C(=O)OC(C)(C)C)C2 Request for Quotation
Chemical Name: tert-Butyl(1R,3S,4S)-3-(6-bromo-1H-benzimidazol-2-yl)-2-azabicyclo[2.2.1]heptane-2-carboxylate (GS-459990)
CAS Number: 1256387-74-2
Product Number: AG009AGO(AGN-PC-0WAJZ2)
Synonyms:
MDL No:
Molecular Formula: C18H22BrN3O2
Molecular Weight: 392.2902

Identification/Properties

Safety Information

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

NMR Spectrum

Other Analytical Data

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Chemical Structure


The compound $name$plays a crucial role in chemical synthesis due to its unique structural features. Specifically, its incorporation in chemical reactions facilitates the formation of structurally complex molecules with intricate stereochemistry. By leveraging the chiral center present in the (1R,3S,4S) configuration, this compound serves as a key building block in the creation of enantiomerically pure compounds. Additionally, the presence of the 6-bromo-1H-benzimidazol-2-yl moiety provides a versatile handle for further functionalization, allowing for the introduction of diverse chemical functionalities. Overall, the application of 1,1-Dimethylethyl (1R,3S,4S)-3-(6-bromo-1H-benzimidazol-2-yl)-2-azabicyclo[2.2.1]heptane-2-carboxylate in chemical synthesis enables the efficient and controlled synthesis of intricate molecular structures with high stereochemical fidelity.