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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-(aminocarbonyl)-, phenylmethyl ester

NC(=O)C1CCCN1C(=O)OCc1ccccc1 Request for Quotation
Chemical Name: 1-Pyrrolidinecarboxylic acid, 2-(aminocarbonyl)-, phenylmethyl ester
CAS Number: 93188-01-3
Product Number: AG00H2YE(AGN-PC-0KRQ7I)
Synonyms:
MDL No:
Molecular Formula: C13H16N2O3
Molecular Weight: 248.2777

Identification/Properties

Computed Properties
Molecular Weight:
248.282g/mol
XLogP3:
0.6
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
4
Exact Mass:
248.116g/mol
Monoisotopic Mass:
248.116g/mol
Topological Polar Surface Area:
72.6A^2
Heavy Atom Count:
18
Formal Charge:
0
Complexity:
313
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

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


Benzyl 2-carbamoylpyrrolidine-1-carboxylate is a versatile compound used in chemical synthesis for its unique properties. In organic chemistry, it serves as a key intermediate in the preparation of various pharmaceuticals and biologically active molecules. Due to its structural characteristics, Benzyl 2-carbamoylpyrrolidine-1-carboxylate can participate in a variety of reactions such as acylations, cyclizations, and functional group transformations, making it an essential building block for creating complex organic compounds. Its utility in the synthesis of diverse chemical entities highlights its importance in the field of medicinal chemistry and drug development.