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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-[[(2,5-dioxo-1-pyrrolidinyl)oxy]carbonyl]-,9H-fluoren-9-ylmethyl ester, (S)-

O=C([C@@H]1CCCN1C(=O)OCC1c2ccccc2c2c1cccc2)ON1C(=O)CCC1=O Request for Quotation
Chemical Name: 1-Pyrrolidinecarboxylic acid, 2-[[(2,5-dioxo-1-pyrrolidinyl)oxy]carbonyl]-,9H-fluoren-9-ylmethyl ester, (S)-
CAS Number: 109074-94-4
Product Number: AG008S95(AGN-PC-0OZ4XN)
Synonyms:
MDL No:
Molecular Formula:
Molecular Weight:

Identification/Properties

Computed Properties
Molecular Weight:
434.448g/mol
XLogP3:
2.8
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
6
Exact Mass:
434.148g/mol
Monoisotopic Mass:
434.148g/mol
Topological Polar Surface Area:
93.2A^2
Heavy Atom Count:
32
Formal Charge:
0
Complexity:
747
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
1
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H317-H319
Precautionary Statements:
P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


Fmoc-Pro-OSu is a key reagent commonly used in chemical synthesis, specifically in the field of peptide synthesis. This compound is utilized as a coupling agent, allowing for the efficient and precise attachment of amino acids during the stepwise assembly of peptides. By incorporating Fmoc-Pro-OSu into the synthesis process, chemists can protect amino groups while activating carboxyl groups, facilitating the formation of stable amide bonds between amino acids. This reagent plays a crucial role in solid-phase peptide synthesis, enabling the controlled elongation of peptide chains with high purity and yield. Additionally, Fmoc-Pro-OSu is known for its compatibility with a variety of amino acids and coupling methods, making it a versatile tool for the synthesis of complex peptides with diverse sequences and functionalities.