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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)-

D-Cysteine,N-[(9H-fluoren-9-ylmethoxy)carbonyl]-S-[(4-methylphenyl)methyl]-

O=C(N[C@@H](C(=O)O)CSCc1ccc(cc1)C)OCC1c2ccccc2c2c1cccc2 Request for Quotation
Chemical Name: D-Cysteine,N-[(9H-fluoren-9-ylmethoxy)carbonyl]-S-[(4-methylphenyl)methyl]-
CAS Number: 200354-41-2
Product Number: AG002CPX(AGN-PC-0QRBDR)
Synonyms:
MDL No:
Molecular Formula: C26H25NO4S
Molecular Weight: 447.5460

Identification/Properties

Computed Properties
Molecular Weight:
447.549g/mol
XLogP3:
5.2
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
9
Exact Mass:
447.15g/mol
Monoisotopic Mass:
447.15g/mol
Topological Polar Surface Area:
101A^2
Heavy Atom Count:
32
Formal Charge:
0
Complexity:
613
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


Fmoc-D-Cys(4-MeBzl)-OH is a valuable building block in chemical synthesis, particularly in the field of peptide synthesis. Due to its unique structure, it allows for precise control over the positioning of cysteine residues within peptide sequences. This specific derivative of cysteine, known for its Fmoc (Fluorenylmethyloxycarbonyl) protection group and 4-Methylbenzyl side chain, offers enhanced stability during peptide assembly and manipulation processes.In peptide synthesis, Fmoc-D-Cys(4-MeBzl)-OH plays a crucial role in introducing cysteine residues at specific locations within the peptide chain. The Fmoc protection group ensures selective deprotection under mild conditions, enabling stepwise assembly of complex peptide sequences. Additionally, the 4-Methylbenzyl side chain provides additional protection and can be selectively removed when needed to allow for further chemical modifications.Overall, the application of Fmoc-D-Cys(4-MeBzl)-OH in chemical synthesis offers chemists precise control over cysteine incorporation in peptide design, making it a versatile tool for the development of custom peptides with specific functionalities.