What is the FMOC-ALA-ALA-OH?

FMOC-ALA-ALA-OH is , while it's Molecular Formula is C21H22N2O5. Used in Pharmaceutical Research and Development: FMOC-ALA-ALA-OH is utilized as a precursor in solid-phase peptide synthesis for the development of pharmaceuticals. Its role is crucial in creating longer, more complex peptides with precise amino acid sequences, which are essential for the discovery and design of new drugs. Used in Biochemistry Research: In the field of biochemistry, FMOC-ALA-ALA-OH is employed as a fundamental component in peptide chemistry. It aids researchers in studying the structure, function, and interactions of peptides, contributing to a deeper understanding of biological processes and the development of bioactive molecules. Used in Peptide Synthesis: FMOC-ALA-ALA-OH is used as a protected amino acid building block in the synthesis of custom peptides. Its application ensures that the alanine residues are correctly incorporated into the desired peptide sequence while maintaining the integrity of the peptide during the assembly process. Used in the Synthesis of Peptide-based Biomaterials: FMOC-ALA-ALA-OH is used as a component in the synthesis of peptide-based biomaterials, such as hydrogels and scaffolds, for applications in tissue engineering and regenerative medicine. The controlled release of bioactive peptides and the promotion of cell adhesion and proliferation are facilitated by the incorporation of this compound into the biomaterials. Used in the Development of Diagnostic and Therapeutic Peptides: FMOC-ALA-ALA-OH is employed in the design and synthesis of diagnostic and therapeutic peptides, including those for imaging, drug delivery, and targeted therapies. Its role in creating specific peptide sequences allows for the development of peptides with tailored properties and functions.

What is the CAS number for FMOC-ALA-ALA-OH?

The CAS number of FMOC-ALA-ALA-OH is 87512-31-0.

What is FMOC-ALA-ALA-OH (87512-31-0) used for?

FMOC-ALA-ALA-OH is a chemical compound that serves as a building block in peptide synthesis, consisting of a chain of three alanine amino acids protected by a fluorenylmethyloxycarbonyl (FMOC) group. This FMOC group shields the amino acids during the synthesis process and can be conveniently removed in the final step, making FMOC-ALA-ALA-OH a versatile component in the creation of complex peptides with specific sequences.

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87512-31-0

Product Name：FMOC-ALA-ALA-OH
Molecular Formula：C21H22N2O5
Purity：99%
Molecular Weight：382.416

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Product Details;

CAS#： 87512-31-0

Molecular Formula： C21H22N2O5

Reputable Manufacturer Supply 87512-31-0 with Cheapest Price, Buy High Quality Fmoc-Ala-Ala-OH

Molecular Formula:C21H22N2O5
Molecular Weight:382.416
Melting Point:175-179℃ (ethyl acetate hexane )
Boiling Point:674.2±45.0 °C(Predicted)
PKA:3.49±0.10(Predicted)
PSA：104.73000
Density:1.280±0.06 g/cm3(Predicted)
LogP:3.28470

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87512-31-0 Process route

: 35661-39-3,136132-75-7
N-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-alanine

: 87512-31-0
(S)-2-((S)-2-((((9H-fluoren-9-yl)methoxy)carbonyl) amino)propanamido)propanoic acid

Conditions

Conditions	Yield
N-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-alanine; With N-ethyl-N,N-diisopropylamine; In dichloromethane; at 20 ℃; for 2.73333h; With piperidine; In N,N-dimethyl-formamide; at 20 ℃; N-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-alanine; Further stages;	78%
Multi-step reaction with 2 steps 1: (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 2 h 2: trifluoroacetic acid / chloroform / 7 h With (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; In tetrahydrofuran; chloroform;
Multi-step reaction with 2 steps 1: dicyclohexyl-carbodiimide / dichloromethane / 6 h / 5 °C 2: sodium hydrogencarbonate / tetrahydrofuran; water / 5 h / 25 °C With sodium hydrogencarbonate; dicyclohexyl-carbodiimide; In tetrahydrofuran; dichloromethane; water;
Multi-step reaction with 2 steps 1: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 10 h / 20 °C 2: lithium hydroxide; water / tetrahydrofuran / 10 h With water; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; lithium hydroxide; In tetrahydrofuran; N,N-dimethyl-formamide;
N-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-alanine; With N-ethyl-N,N-diisopropylamine; In N,N-dimethyl-formamide; With piperidine; In N,N-dimethyl-formamide; N-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-alanine; Further stages;

: 56-41-7,25191-17-7,18875-37-1
L-alanin

: 73724-40-0
(S)-2,5-dioxopyrrolidin-1-yl 2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)propanoate

: 87512-31-0
(S)-2-((S)-2-((((9H-fluoren-9-yl)methoxy)carbonyl) amino)propanamido)propanoic acid