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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)-

FMOC-D-HOMOLEUCINE

CC(CC[C@H](C(=O)O)NC(=O)OCC1c2ccccc2c2c1cccc2)C Request for Quotation
Chemical Name: FMOC-D-HOMOLEUCINE
CAS Number: 204320-60-5
Product Number: AG0029F7(AGN-PC-0WADCK)
Synonyms:
MDL No:
Molecular Formula: C22H25NO4
Molecular Weight: 367.4382

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
367.445g/mol
XLogP3:
4.7
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
8
Exact Mass:
367.178g/mol
Monoisotopic Mass:
367.178g/mol
Topological Polar Surface Area:
75.6A^2
Heavy Atom Count:
27
Formal Charge:
0
Complexity:
498
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


N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-5-methyl-D-norleucine is a versatile compound widely utilized in chemical synthesis for its unique reactivity and structural properties. This compound acts as a valuable building block in the creation of various pharmaceuticals, agrochemicals, and specialty chemicals. With its specific chemical structure, N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-5-methyl-D-norleucine serves as a key intermediate in the synthesis of complex organic molecules, allowing for the efficient and controlled formation of bonds crucial for the development of novel compounds. Its strategic incorporation in synthetic pathways enables chemists to access diverse molecular architectures, facilitating the exploration of new chemical entities with potential applications in drug discovery, materials science, and other fields requiring tailored chemical structures.