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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)-

3-[9H-fluoren-9-ylmethoxycarbonyl(methyl)amino]propanoic acid

OC(=O)CCN(C(=O)OCC1c2ccccc2c2c1cccc2)C Request for Quotation
Chemical Name: 3-[9H-fluoren-9-ylmethoxycarbonyl(methyl)amino]propanoic acid
CAS Number: 172965-84-3
Product Number: AG003T17(AGN-PC-00OQOG)
Synonyms:
MDL No: MFCD01861327
Molecular Formula: C19H19NO4
Molecular Weight: 325.3585

Identification/Properties

Properties
BP:
525.4±29.0 °C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
325.364g/mol
XLogP3:
2.7
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
6
Exact Mass:
325.131g/mol
Monoisotopic Mass:
325.131g/mol
Topological Polar Surface Area:
66.8A^2
Heavy Atom Count:
24
Formal Charge:
0
Complexity:
444
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

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


N-Fmoc-N-Methyl-beta-alanine is commonly utilized in chemical synthesis as a versatile building block for the preparation of peptide and pharmaceutical compounds. Its Fmoc (9-fluorenylmethoxycarbonyl) protected amino group allows for selective deprotection under mild conditions, enabling the sequential assembly of peptides with high purity. This compound is particularly valuable in solid-phase peptide synthesis, where the Fmoc group serves as a temporary protecting group during the coupling of amino acids, leading to the controlled elongation of the peptide chain. Additionally, the presence of the N-Methyl group enhances the stability and solubility of the compound in various organic solvents, facilitating its incorporation into complex molecular structures. Furthermore, the unique properties of N-Fmoc-N-Methyl-beta-alanine make it an essential tool for the development of novel peptide-based therapeutics and bioactive compounds.