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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-meabu(4)-OH

OC(=O)CCCN(C(=O)OCC1c2ccccc2c2c1cccc2)C Request for Quotation
Chemical Name: Fmoc-meabu(4)-OH
CAS Number: 221124-57-8
Product Number: AG00BGJY(AGN-PC-0WOHHO)
Synonyms:
MDL No:
Molecular Formula: C20H21NO4
Molecular Weight: 339.3850

Identification/Properties

Computed Properties
Molecular Weight:
339.391g/mol
XLogP3:
3.1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
7
Exact Mass:
339.147g/mol
Monoisotopic Mass:
339.147g/mol
Topological Polar Surface Area:
66.8A^2
Heavy Atom Count:
25
Formal Charge:
0
Complexity:
458
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
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


4-[[(9H-Fluoren-9-ylmethoxy)carbonyl]methylamino]butanoic acid, also known as $name$, is a versatile compound widely used in chemical synthesis. This compound serves as a key building block in the creation of various pharmaceuticals, agrochemicals, and materials due to its unique reactivity and functional groups. In chemical synthesis, $name$ is utilized as a protected amino acid derivative, allowing for controlled and selective reactions at specific sites on the molecule. By incorporating this compound into synthetic pathways, chemists can efficiently introduce amino acid functionality while protecting other reactive groups, thereby facilitating the synthesis of complex molecules with high precision and purity. Additionally, the fluorenylmethoxycarbonyl (Fmoc) group on $name$ can be readily removed under mild conditions, making it a valuable tool in peptide synthesis for the sequential deprotection of amino acids. Overall, the application of 4-[[(9H-Fluoren-9-ylmethoxy)carbonyl]methylamino]butanoic acid in chemical synthesis enables the efficient and controlled construction of diverse molecular architectures with potential applications in various fields of chemistry and beyond.