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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)-

L-leucine, 4-fluoro-, ethyl ester-4×H2SO4×½Py

c1cccnc1.OS(=O)(=O)O.OS(=O)(=O)O.CCOC(=O)[C@H](CC(F)(C)C)N.CCOC(=O)[C@H](CC(F)(C)C)N Request for Quotation
Chemical Name: L-leucine, 4-fluoro-, ethyl ester-4×H2SO4×½Py
CAS Number: 1459196-65-6
Product Number: AG001DIC(AGN-PC-0WAJ04)
Synonyms:
MDL No:
Molecular Formula: C21H41F2N3O12S2
Molecular Weight: 629.6899

Identification/Properties

Properties
Storage:
Room Temperature;
Form:
Solid

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


$Name$ is a versatile chemical compound that finds a valuable application in chemical synthesis, specifically in the realm of organic chemistry. As a derivative of L-leucine with a 4-fluoro substitution and an ethyl ester functional group, this compound plays a crucial role as a building block in the creation of various complex organic molecules.In chemical synthesis, $Name$ serves as a key intermediate in the production of pharmaceuticals, agrochemicals, and fine chemicals. Its unique structure and reactivity allow for specific modifications and transformations, enabling chemists to tailor the properties of the final products. By incorporating $Name$ into synthetic pathways, researchers can introduce fluorine atoms and ethyl ester groups with precision, leading to the development of novel compounds with enhanced biological activities or improved chemical properties.Moreover, the strategic placement of the 4-fluoro and ethyl ester moieties on the L-leucine scaffold offers opportunities for selective functionalization and stereochemical control during the synthesis process. This level of control is essential for achieving high yields and desired stereochemistry in the target molecules, making $Name$ a valuable tool for synthetic chemists working on intricate organic synthesis projects.Overall, the application of L-leucine, 4-fluoro-, ethyl ester-4h2so4py in chemical synthesis underscores its importance as a versatile building block for the generation of structurally diverse and functionally rich compounds in the field of organic chemistry.