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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)-

(2R)-pyrrolidine-2-carboxamide;hydrochloride

NC(=O)C1CCCN1.Cl Request for Quotation
Chemical Name: (2R)-pyrrolidine-2-carboxamide;hydrochloride
CAS Number: 115630-49-4
Product Number: AG000GA5(AGN-PC-07XRM9)
Synonyms:
MDL No:
Molecular Formula: C5H11ClN2O
Molecular Weight: 150.6066

Identification/Properties

Computed Properties
Molecular Weight:
150.606g/mol
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
150.056g/mol
Monoisotopic Mass:
150.056g/mol
Topological Polar Surface Area:
55.1A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
103
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:
2
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


H-DL-Pro-NH2.HCl is a valuable chemical reagent commonly used in peptide synthesis. Specifically, it serves as a key building block in the creation of peptides and proteins through solid-phase peptide synthesis (SPPS) methodologies. By incorporating H-DL-Pro-NH2.HCl into the synthesis process, chemists can efficiently construct and assemble complex peptide structures with high precision. This compound plays a critical role in enabling the formation of peptide bonds and facilitating the sequential coupling of amino acid residues. Additionally, H-DL-Pro-NH2.HCl offers excellent compatibility with various protecting groups and activation methods, making it a versatile and essential tool for peptide chemists working in the field of chemical synthesis.