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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)-

1-Pyrrolidinecarboxylic acid, 2-(aminomethyl)-, phenylmethyl ester

NCC1CCCN1C(=O)OCc1ccccc1 Request for Quotation
Chemical Name: 1-Pyrrolidinecarboxylic acid, 2-(aminomethyl)-, phenylmethyl ester
CAS Number: 119020-03-0
Product Number: AG000P2T(AGN-PC-0KKL3D)
Synonyms:
MDL No:
Molecular Formula: C13H18N2O2
Molecular Weight: 234.2942

Identification/Properties

Computed Properties
Molecular Weight:
234.299g/mol
XLogP3:
1.2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
4
Exact Mass:
234.137g/mol
Monoisotopic Mass:
234.137g/mol
Topological Polar Surface Area:
55.6A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
252
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

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NMR Spectrum

Other Analytical Data

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Chemical Structure


Benzyl 2-(aminomethyl)pyrrolidine-1-carboxylate is a versatile compound frequently employed in chemical synthesis due to its unique properties and reactivity. In the field of organic chemistry, this compound serves as a valuable building block for the synthesis of various complex molecules. Its amino group can participate in a range of reactions, making it an essential component in the creation of pharmaceuticals, agrochemicals, and materials. Additionally, the presence of the pyrrolidine ring enhances the compound's stability and contributes to its stereochemical properties, allowing for precise control over the configuration of the resulting products. In summary, Benzyl 2-(aminomethyl)pyrrolidine-1-carboxylate is a crucial intermediate in the synthesis of diverse chemical compounds with broad applications in various industries.