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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)-

Fmoc-amcp-oh

O=C(NCC1(CC1)C(=O)O)OCC1c2ccccc2c2c1cccc2 Request for Quotation
Chemical Name: Fmoc-amcp-oh
CAS Number: 1263045-62-0
Product Number: AG009C2O(AGN-PC-0WNPPY)
Synonyms:
MDL No:
Molecular Formula:
Molecular Weight:

Identification/Properties

Computed Properties
Molecular Weight:
337.375g/mol
XLogP3:
2.9
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
6
Exact Mass:
337.131g/mol
Monoisotopic Mass:
337.131g/mol
Topological Polar Surface Area:
75.6A^2
Heavy Atom Count:
25
Formal Charge:
0
Complexity:
508
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


Fmoc-amcp-oh, a versatile compound used in chemical synthesis, plays a crucial role in the field of organic chemistry. Its primary application lies in solid-phase peptide synthesis, a technique widely employed to construct peptides and small proteins in a stepwise manner. By utilizing Fmoc-amcp-oh as a protecting group, chemists can selectively shield specific amino acid residues during the peptide assembly process. This protection allows for efficient and precise control over peptide bond formation, ultimately leading to the creation of complex and tailored peptide sequences. Furthermore, Fmoc-amcp-oh exhibits excellent stability under the typical conditions of peptide synthesis, ensuring reliable performance throughout the reaction. Its compatibility with various coupling reagents and purification methods further enhances its utility in peptide chemistry. Overall, Fmoc-amcp-oh is a vital tool for researchers and chemists engaged in the synthesis of peptides and related biomolecules, enabling the advancement of diverse applications in drug development, biotechnology, and chemical biology.