Boc-Phe(3-Me)-OH
Boc-Phe(3-Me)-OH (CAS: 114873-06-2), with the molecular formula C15H21NO4 and a molecular weight of 279.33 g/mol, is a derivative of phenylalanine. This unnatural amino acid derivative is commonly employed in peptide chemistry for the synthesis of modified peptides. Its structure allows for specific incorporation into peptide chains, facilitating research in chemical biology and advanced chemical synthesis.
- IUPAC
- Boc-3-methyl-L-phenylalanine

Peptide Synthesis
Boc-3-methyl-L-phenylalanine is a protected unnatural amino acid used in solid-phase and solution-phase peptide synthesis. It enables the introduction of modified phenylalanine residues into peptide sequences to study structure-activity relationships or to create novel peptidomimetics.
Chemical Biology Research
As an unnatural amino acid derivative, it serves as a valuable building block in chemical biology for constructing peptides with altered properties or functionalities. This aids in probing biological pathways and developing new therapeutic agents.
Organic Synthesis
This compound is utilised as a chiral intermediate in complex organic synthesis. Its specific structure can be leveraged in multi-step synthetic routes towards diverse target molecules.
| Molecular weight | 279.33 |
|---|---|
| Empirical formula | C15H21NO4 |
| Assay | ≥98.0% (TLC) |
| Protective equipment | Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter |
|---|---|
| Water hazard class (WGK, DE) | 3 |
Hazard information is provided for guidance. Always consult the product Safety Data Sheet (SDS), available on request, before handling.
Documentation
Every batch ships with a Certificate of Analysis covering assay, identity and purity; the grade is confirmed against your enquiry. Safety Data Sheets and technical data sheets are available on request.
Supply & logistics
Samples for technical evaluation; bulk MOQ by grade and packaging. In-stock material ships in 7–10 working days, worldwide, with full export documentation.
What is Boc-Phe(3-Me)-OH used for?
+
Boc-Phe(3-Me)-OH is primarily used as a protected unnatural amino acid derivative in peptide synthesis and for research in chemical biology and organic synthesis.
What is the CAS number and molecular formula of Boc-Phe(3-Me)-OH?
+
The CAS number is 114873-06-2, and the molecular formula is C15H21NO4.
What grade and purity does Tech Serve Solutions supply?
+
Tech Serve Solutions supplies Boc-Phe(3-Me)-OH with an assay of ≥98.0% (TLC). We do not represent this product as USP, BP, or EP grade.
What are the safety and handling precautions for Boc-Phe(3-Me)-OH?
+
Users should employ appropriate personal protective equipment, including eyeshields and gloves. A type N95 (US) or type P1 (EN143) respirator filter is recommended. The compound is classified with WGK 3 in Germany, indicating a significant hazard to water.
How is Boc-Phe(3-Me)-OH packed and shipped?
+
Tech Serve Solutions expertly packs and ships fine chemicals, pharmaceutical intermediates, and laboratory reagents globally, adhering to all relevant regulations for safe transport.
How can I request a sample or quote for Boc-Phe(3-Me)-OH?
+
To request a sample or quote, please use the contact form on our website or call our sales team directly. Our experts will assist you promptly.
▶ Related products

1-(2-Fluorobenzyl)piperazine
C11H15FN2
Chemical Synthesis
1-(2-Fluorophenyl)biguanide hydrochloride
Chemical Synthesis

1-(2-Fluorophenyl)cyclopropanecarboxylic acid
C10H9FO2
Chemical Synthesis
1-(2-Fluorophenyl)piperazine
C10H13FN2
Chemical Synthesis
1-(2-Fluorophenyl)piperazine monohydrochloride
C10H13FN2 · HCl
Chemical Synthesis
1-(2-Furoyl)-1H-benzotriazole
C11H7N3O2
Chemical Synthesis
1-(2-Furoyl)piperazine
C9H12N2O2
Chemical Synthesis
1-(2-Hydroxy-5-methylphenyl)-3-phenyl-1,3-propanedione
Chemical Synthesis
▶ Explore more

3-Methyl-1,5-di-p-tolyl-1,4-pentazadiene
Chemical Synthesis

3-Methyl-1,5-pentanediol
Chemical Synthesis

3-Methyl-1-(2-methylphenyl)-1H-pyrazol-5-amine
C11H13N3
Chemical Synthesis
3-Methyl-1-(3′-sulfoamidophenyl)-5-pyrazolone
C10H11N3O3S
Chemical Synthesis