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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-Methionine, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-

CSCC[C@H](C(=O)O)NC(=O)OCC1c2ccccc2c2c1cccc2 Request for Quotation
Chemical Name: D-Methionine, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-
CAS Number: 112883-40-6
Product Number: AG0078PW(AGN-PC-0NY136)
Synonyms:
MDL No:
Molecular Formula: C20H21NO4S
Molecular Weight: 371.4500

Identification/Properties

Computed Properties
Molecular Weight:
371.451g/mol
XLogP3:
3.7
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
8
Exact Mass:
371.119g/mol
Monoisotopic Mass:
371.119g/mol
Topological Polar Surface Area:
101A^2
Heavy Atom Count:
26
Formal Charge:
0
Complexity:
478
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:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


Fmoc-D-Met-OH, also known as Fmoc-D-methionine, is a crucial building block in chemical synthesis processes. This compound is commonly utilized in peptide synthesis, which is a fundamental aspect of pharmaceutical and biotechnological research.In peptide synthesis, Fmoc-D-Met-OH serves as a protected form of D-methionine amino acid. The Fmoc (Fluorenylmethyloxycarbonyl) protecting group shields the amine group of methionine, allowing for selective reactions to occur at other functional groups present in the peptide chain. This protection strategy enables precise and controlled peptide assembly, thus contributing to the successful creation of complex peptides and proteins.Moreover, Fmoc-D-Met-OH plays a crucial role in solid-phase peptide synthesis (SPPS), a popular method for constructing peptides. Through strategic deprotection and coupling steps, Fmoc-D-Met-OH can be sequentially added to the growing peptide chain anchored to a solid support, facilitating the stepwise synthesis of peptides with high purity and efficiency.Overall, Fmoc-D-Met-OH's application in chemical synthesis, particularly in peptide synthesis and SPPS, highlights its significance in enabling the efficient and precise construction of peptides and proteins for various research and industrial purposes.