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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)-

Glycine, N-[N-[N-[N-[(phenylmethoxy)carbonyl]glycyl]glycyl]glycyl]-

O=C(CNC(=O)OCc1ccccc1)NCC(=O)NCC(=O)NCC(=O)O Request for Quotation
Chemical Name: Glycine, N-[N-[N-[N-[(phenylmethoxy)carbonyl]glycyl]glycyl]glycyl]-
CAS Number: 7770-50-5
Product Number: AG00G4B9(AGN-PC-0JMGHH)
Synonyms:
MDL No:
Molecular Formula: C16H20N4O7
Molecular Weight: 380.3526

Identification/Properties

Computed Properties
Molecular Weight:
380.357g/mol
XLogP3:
-0.9
Hydrogen Bond Donor Count:
5
Hydrogen Bond Acceptor Count:
7
Rotatable Bond Count:
11
Exact Mass:
380.133g/mol
Monoisotopic Mass:
380.133g/mol
Topological Polar Surface Area:
163A^2
Heavy Atom Count:
27
Formal Charge:
0
Complexity:
547
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


Z-Gly-Gly-Gly-Gly-OH, also known as Z-GGGG-OH, is a peptide derivative commonly used in chemical synthesis. This compound is primarily utilized as a building block in peptide synthesis and solid-phase peptide synthesis to construct complex peptide molecules. Z-GGGG-OH plays a crucial role in forming peptide bonds and creating peptide chains through sequential coupling reactions. Its selective functional groups allow for precise control over the peptide sequence, making it a versatile tool in peptide chemistry. Additionally, Z-GGGG-OH can also be employed as a protecting group to shield reactive functional groups in peptides, preventing undesired side reactions during synthesis. Overall, the application of Z-Gly-Gly-Gly-Gly-OH in chemical synthesis enables the efficient and controlled production of customized peptides for various research and pharmaceutical purposes.