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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)-

Bicyclo[2.2.1]hept-5-ene-2-carboxylic acid, 3-amino-,(1R,2R,3S,4S)-rel-

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Chemical Name: Bicyclo[2.2.1]hept-5-ene-2-carboxylic acid, 3-amino-,(1R,2R,3S,4S)-rel-
CAS Number: 92511-32-5
Product Number: AG00GV96(AGN-PC-0VZUBL)
Synonyms:
MDL No:
Molecular Formula:
Molecular Weight:

Identification/Properties

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H312-H332
Precautionary Statements:
P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P330-P362-P403+P233-P501
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The 3-exo-Aminobicyclo[2.2.1]hept-5-ene-2-carboxylic acid plays a crucial role in chemical synthesis as a versatile intermediate. Its unique structure and functional groups make it an ideal building block for the synthesis of various complex organic molecules. One key application of this compound is in the preparation of novel heterocyclic compounds. By utilizing the amino and carboxylic acid groups present in 3-exo-Aminobicyclo[2.2.1]hept-5-ene-2-carboxylic acid, chemists can introduce additional functional groups through a variety of synthetic transformations. This enables the creation of diverse and structurally complex heterocycles that have potential applications in pharmaceuticals, agrochemicals, and materials science.Furthermore, the stereochemistry of the bicyclic ring system in 3-exo-Aminobicyclo[2.2.1]hept-5-ene-2-carboxylic acid can be leveraged to control the spatial arrangement of substituents in the final products. This can be particularly important in drug discovery and development, where the three-dimensional arrangement of atoms can significantly influence the biological activity and pharmacological properties of a compound.Overall, the strategic use of 3-exo-Aminobicyclo[2.2.1]hept-5-ene-2-carboxylic acid in chemical synthesis allows for the efficient construction of complex molecules with precise control over stereochemistry, making it a valuable tool for synthetic chemists working in a variety of research areas.