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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)-

Carbamic acid, [(1S)-1-(chlorocarbonyl)-2-methylpropyl]-,9H-fluoren-9-ylmethyl ester

O=C(N[C@H](C(=O)Cl)C(C)C)OCC1c2ccccc2c2c1cccc2 Request for Quotation
Chemical Name: Carbamic acid, [(1S)-1-(chlorocarbonyl)-2-methylpropyl]-,9H-fluoren-9-ylmethyl ester
CAS Number: 103321-53-5
Product Number: AG008S9C(AGN-PC-0OSBT2)
Synonyms:
MDL No:
Molecular Formula: C20H20ClNO3
Molecular Weight: 357.8307

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Chemical Structure


Fmoc-Val-Cl is a valuable reagent widely utilized in chemical synthesis for the efficient protection of amino groups in peptide synthesis. This compound plays a crucial role in the solid-phase peptide synthesis process, where it is commonly used as a protecting group for the amino acid valine. By selectively blocking the amino group of valine with the Fmoc protecting group, Fmoc-Val-Cl enables the stepwise assembly of peptides with high purity and yields. Furthermore, the Fmoc protecting group can be easily removed under mild conditions, making it a versatile tool in peptide chemistry. Overall, Fmoc-Val-Cl is an essential reagent in the synthesis of complex peptides and peptidomimetics, offering chemists precise control over the sequence and structure of the final product.