Benzenebutanoic acid, b-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-,(bS)-|193954-28-8,AngeneChemical

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Pyrimidine, 5-bromo-2-methyl-

1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide

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)-

Benzenebutanoic acid, b-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-,(bS)-

OC(=O)C[C@H](Cc1ccccc1)NC(=O)OCC1c2ccccc2c2c1cccc2

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Chemical Name:	Benzenebutanoic acid, b-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-,(bS)-
CAS Number:	193954-28-8
Product Number:	AG0034YC(AGN-PC-0QMH5J)
Synonyms:
MDL No:
Molecular Formula:	C25H23NO4
Molecular Weight:	401.4544

Identification/Properties
Safety Information
NMR Spectrum
Other Analytical Data
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Identification/Properties

Properties

MP:

110-112℃(Solv: ethyl acetate (141-78-6); hexane (110-54-3))

BP:

633.2°C at 760 mmHg

Storage:

Keep in dry area;2-8℃;

Form:

Solid

Computed Properties

Molecular Weight:

401.462g/mol

XLogP3:

4.6

Hydrogen Bond Donor Count:

Hydrogen Bond Acceptor Count:

Rotatable Bond Count:

Exact Mass:

401.163g/mol

Monoisotopic Mass:

401.163g/mol

Topological Polar Surface Area:

75.6A^2

Heavy Atom Count:

Formal Charge:

Complexity:

566

Isotope Atom Count:

Defined Atom Stereocenter Count:

Undefined Atom Stereocenter Count:

Defined Bond Stereocenter Count:

Undefined Bond Stereocenter Count:

Covalently-Bonded Unit Count:

Compound Is Canonicalized:

Yes

Safety Information

GHS Pictogram:

Signal Word:

Warning

UN#:

N/A

Hazard Statements:

H302-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-L-β-HoPhe-OH, a derivative of the amino acid β-homophenylalanine, is a valuable reagent widely used in chemical synthesis for its unique properties and versatile applications. This compound serves as a crucial building block in peptide synthesis, particularly in the solid-phase synthesis of peptide chains. Due to the Fmoc (9-fluorenylmethyloxycarbonyl) protecting group attached to the amino group of L-β-HoPhe-OH, this reagent facilitates controlled and efficient peptide bond formation during the peptide assembly process.The Fmoc-L-β-HoPhe-OH compound is known for its compatibility with standard solid-phase peptide synthesis protocols and its ability to enable the incorporation of β-homophenylalanine residues into peptide sequences. Additionally, the Fmoc protecting group can be selectively removed under mild acidic conditions, allowing for the sequential addition of other amino acids and modifications to the growing peptide chain. This reagent is particularly valuable in the synthesis of bioactive peptides, peptidomimetics, and other structurally diverse peptides with enhanced stability and biological activity.In summary, Fmoc-L-β-HoPhe-OH plays a crucial role in the efficient and precise synthesis of complex peptides, offering chemists a powerful tool for the development of novel peptide-based therapeutics, materials, and biochemical probes.