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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)-

methyl 3-amino-1-benzylpyrrolidine-3-carboxylate

COC(=O)C1(N)CCN(C1)Cc1ccccc1 Request for Quotation
Chemical Name: methyl 3-amino-1-benzylpyrrolidine-3-carboxylate
CAS Number: 145602-88-6
Product Number: AG001D8E(AGN-PC-0N4JT1)
Synonyms:
MDL No:
Molecular Formula: C13H18N2O2
Molecular Weight: 234.2942

Identification/Properties

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


Methyl 3-amino-1-benzylpyrrolidine-3-carboxylate is a versatile compound commonly used in chemical synthesis processes. This compound serves as a crucial building block in the creation of various pharmaceuticals and fine chemicals due to its unique structure and reactivity. In organic synthesis, Methyl 3-amino-1-benzylpyrrolidine-3-carboxylate can undergo diverse transformations to introduce functional groups or form complex molecular structures. Its presence in a synthetic route enables the production of biologically active molecules, such as pharmaceutical intermediates and natural products. Additionally, the incorporation of this compound in the synthesis of heterocyclic compounds allows for the development of novel materials with potential applications in medicinal chemistry and material science. The strategic utilization of Methyl 3-amino-1-benzylpyrrolidine-3-carboxylate in chemical transformations highlights its significance in advancing synthetic methodologies and expanding the scope of organic chemistry research.